# HG changeset patch
# User fubar
# Date 1375855108 14400
# Node ID 48d71bd383a1f12a4524b2876006762164cf7eb1
# Parent 37b851eb82033c12fdb550e847e8b40ee302b3c8
Uploaded
diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/.hg_archival.txt
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/.hg_archival.txt Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,5 @@
+repo: 2122e630b13aedc43ced5f83c11988903db28ea6
+node: 37b851eb82033c12fdb550e847e8b40ee302b3c8
+branch: default
+latesttag: null
+latesttagdistance: 24
diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/rgToolFactory.py
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/rgToolFactory.py Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,631 @@
+# rgToolFactory.py
+# see https://bitbucket.org/fubar/galaxytoolfactory/wiki/Home
+#
+# copyright ross lazarus (ross stop lazarus at gmail stop com) May 2012
+#
+# all rights reserved
+# Licensed under the LGPL
+# suggestions for improvement and bug fixes welcome at https://bitbucket.org/fubar/galaxytoolfactory/wiki/Home
+#
+# august 2013
+# found a problem with GS if $TMP or $TEMP missing - now inject /tmp and warn
+#
+# july 2013
+# added ability to combine images and individual log files into html output
+# just make sure there's a log file foo.log and it will be output
+# together with all images named like "foo_*.pdf
+# otherwise old format for html
+#
+# January 2013
+# problem pointed out by Carlos Borroto
+# added escaping for <>$ - thought I did that ages ago...
+#
+# August 11 2012
+# changed to use shell=False and cl as a sequence
+
+# This is a Galaxy tool factory for simple scripts in python, R or whatever ails ye.
+# It also serves as the wrapper for the new tool.
+#
+# you paste and run your script
+# Only works for simple scripts that read one input from the history.
+# Optionally can write one new history dataset,
+# and optionally collect any number of outputs into links on an autogenerated HTML page.
+
+# DO NOT install on a public or important site - please.
+
+# installed generated tools are fine if the script is safe.
+# They just run normally and their user cannot do anything unusually insecure
+# but please, practice safe toolshed.
+# Read the fucking code before you install any tool
+# especially this one
+
+# After you get the script working on some test data, you can
+# optionally generate a toolshed compatible gzip file
+# containing your script safely wrapped as an ordinary Galaxy script in your local toolshed for
+# safe and largely automated installation in a production Galaxy.
+
+# If you opt for an HTML output, you get all the script outputs arranged
+# as a single Html history item - all output files are linked, thumbnails for all the pdfs.
+# Ugly but really inexpensive.
+#
+# Patches appreciated please.
+#
+#
+# long route to June 2012 product
+# Behold the awesome power of Galaxy and the toolshed with the tool factory to bind them
+# derived from an integrated script model
+# called rgBaseScriptWrapper.py
+# Note to the unwary:
+# This tool allows arbitrary scripting on your Galaxy as the Galaxy user
+# There is nothing stopping a malicious user doing whatever they choose
+# Extremely dangerous!!
+# Totally insecure. So, trusted users only
+#
+# preferred model is a developer using their throw away workstation instance - ie a private site.
+# no real risk. The universe_wsgi.ini admin_users string is checked - only admin users are permitted to run this tool.
+#
+
+import sys
+import shutil
+import subprocess
+import os
+import time
+import tempfile
+import optparse
+import tarfile
+import re
+import shutil
+import math
+
+progname = os.path.split(sys.argv[0])[1]
+myversion = 'V000.2 June 2012'
+verbose = False
+debug = False
+toolFactoryURL = 'https://bitbucket.org/fubar/galaxytoolfactory'
+
+def timenow():
+ """return current time as a string
+ """
+ return time.strftime('%d/%m/%Y %H:%M:%S', time.localtime(time.time()))
+
+html_escape_table = {
+ "&": "&",
+ ">": ">",
+ "<": "<",
+ "$": "\$"
+ }
+
+def html_escape(text):
+ """Produce entities within text."""
+ return "".join(html_escape_table.get(c,c) for c in text)
+
+def cmd_exists(cmd):
+ return subprocess.call("type " + cmd, shell=True,
+ stdout=subprocess.PIPE, stderr=subprocess.PIPE) == 0
+
+
+class ScriptRunner:
+ """class is a wrapper for an arbitrary script
+ """
+
+ def __init__(self,opts=None,treatbashSpecial=True):
+ """
+ cleanup inputs, setup some outputs
+
+ """
+ self.useGM = cmd_exists('gm')
+ self.useIM = cmd_exists('convert')
+ self.useGS = cmd_exists('gs')
+ self.temp_warned = False # we want only one warning if $TMP not set
+ self.treatbashSpecial = treatbashSpecial
+ if opts.output_dir: # simplify for the tool tarball
+ os.chdir(opts.output_dir)
+ self.thumbformat = 'png'
+ self.opts = opts
+ self.toolname = re.sub('[^a-zA-Z0-9_]+', '', opts.tool_name) # a sanitizer now does this but..
+ self.toolid = self.toolname
+ self.myname = sys.argv[0] # get our name because we write ourselves out as a tool later
+ self.pyfile = self.myname # crude but efficient - the cruft won't hurt much
+ self.xmlfile = '%s.xml' % self.toolname
+ s = open(self.opts.script_path,'r').readlines()
+ s = [x.rstrip() for x in s] # remove pesky dos line endings if needed
+ self.script = '\n'.join(s)
+ fhandle,self.sfile = tempfile.mkstemp(prefix=self.toolname,suffix=".%s" % (opts.interpreter))
+ tscript = open(self.sfile,'w') # use self.sfile as script source for Popen
+ tscript.write(self.script)
+ tscript.close()
+ self.indentedScript = '\n'.join([' %s' % x for x in s]) # for restructured text in help
+ self.escapedScript = '\n'.join([html_escape(x) for x in s])
+ self.elog = os.path.join(self.opts.output_dir,"%s_error.log" % self.toolname)
+ if opts.output_dir: # may not want these complexities
+ self.tlog = os.path.join(self.opts.output_dir,"%s_runner.log" % self.toolname)
+ art = '%s.%s' % (self.toolname,opts.interpreter)
+ artpath = os.path.join(self.opts.output_dir,art) # need full path
+ artifact = open(artpath,'w') # use self.sfile as script source for Popen
+ artifact.write(self.script)
+ artifact.close()
+ self.cl = []
+ self.html = []
+ a = self.cl.append
+ a(opts.interpreter)
+ if self.treatbashSpecial and opts.interpreter in ['bash','sh']:
+ a(self.sfile)
+ else:
+ a('-') # stdin
+ a(opts.input_tab)
+ a(opts.output_tab)
+ self.outFormats = 'tabular' # TODO make this an option at tool generation time
+ self.inputFormats = 'tabular' # TODO make this an option at tool generation time
+ self.test1Input = '%s_test1_input.xls' % self.toolname
+ self.test1Output = '%s_test1_output.xls' % self.toolname
+ self.test1HTML = '%s_test1_output.html' % self.toolname
+
+ def makeXML(self):
+ """
+ Create a Galaxy xml tool wrapper for the new script as a string to write out
+ fixme - use templating or something less fugly than this example of what we produce
+
+
+ a tabular file
+
+ reverse.py --script_path "$runMe" --interpreter "python"
+ --tool_name "reverse" --input_tab "$input1" --output_tab "$tab_file"
+
+
+
+
+
+
+
+
+
+
+
+**What it Does**
+
+Reverse the columns in a tabular file
+
+
+
+
+
+# reverse order of columns in a tabular file
+import sys
+inp = sys.argv[1]
+outp = sys.argv[2]
+i = open(inp,'r')
+o = open(outp,'w')
+for row in i:
+ rs = row.rstrip().split('\t')
+ rs.reverse()
+ o.write('\t'.join(rs))
+ o.write('\n')
+i.close()
+o.close()
+
+
+
+
+
+
+ """
+ newXML="""
+ %(tooldesc)s
+ %(command)s
+
+ %(inputs)s
+
+
+ %(outputs)s
+
+
+
+ %(script)s
+
+
+ %(tooltests)s
+
+ %(help)s
+
+ """ # needs a dict with toolname, toolid, interpreter, scriptname, command, inputs as a multi line string ready to write, outputs ditto, help ditto
+
+ newCommand="""
+ %(toolname)s.py --script_path "$runMe" --interpreter "%(interpreter)s"
+ --tool_name "%(toolname)s" %(command_inputs)s %(command_outputs)s
+ """ # may NOT be an input or htmlout
+ tooltestsTabOnly = """
+
+
+
+
+ """
+ tooltestsHTMLOnly = """
+
+
+
+
+ """
+ tooltestsBoth = """
+
+
+
+
+
+ """
+ xdict = {}
+ xdict['tool_version'] = self.opts.tool_version
+ xdict['test1Input'] = self.test1Input
+ xdict['test1HTML'] = self.test1HTML
+ xdict['test1Output'] = self.test1Output
+ if self.opts.make_HTML and self.opts.output_tab <> 'None':
+ xdict['tooltests'] = tooltestsBoth % xdict
+ elif self.opts.make_HTML:
+ xdict['tooltests'] = tooltestsHTMLOnly % xdict
+ else:
+ xdict['tooltests'] = tooltestsTabOnly % xdict
+ xdict['script'] = self.escapedScript
+ # configfile is least painful way to embed script to avoid external dependencies
+ # but requires escaping of <, > and $ to avoid Mako parsing
+ if self.opts.help_text:
+ xdict['help'] = open(self.opts.help_text,'r').read()
+ else:
+ xdict['help'] = 'Please ask the tool author for help as none was supplied at tool generation'
+ coda = ['**Script**','Pressing execute will run the following code over your input file and generate some outputs in your history::']
+ coda.append(self.indentedScript)
+ coda.append('**Attribution** This Galaxy tool was created by %s at %s\nusing the Galaxy Tool Factory.' % (self.opts.user_email,timenow()))
+ coda.append('See %s for details of that project' % (toolFactoryURL))
+ coda.append('Please cite: Creating re-usable tools from scripts: The Galaxy Tool Factory. Ross Lazarus; Antony Kaspi; Mark Ziemann; The Galaxy Team. ')
+ coda.append('Bioinformatics 2012; doi: 10.1093/bioinformatics/bts573')
+ xdict['help'] = '%s\n%s' % (xdict['help'],'\n'.join(coda))
+ if self.opts.tool_desc:
+ xdict['tooldesc'] = '%s ' % self.opts.tool_desc
+ else:
+ xdict['tooldesc'] = ''
+ xdict['command_outputs'] = ''
+ xdict['outputs'] = ''
+ if self.opts.input_tab <> 'None':
+ xdict['command_inputs'] = '--input_tab "$input1" ' # the space may matter a lot if we append something
+ xdict['inputs'] = ' \n' % self.inputFormats
+ else:
+ xdict['command_inputs'] = '' # assume no input - eg a random data generator
+ xdict['inputs'] = ''
+ xdict['inputs'] += ' \n' % self.toolname
+ xdict['toolname'] = self.toolname
+ xdict['toolid'] = self.toolid
+ xdict['interpreter'] = self.opts.interpreter
+ xdict['scriptname'] = self.sfile
+ if self.opts.make_HTML:
+ xdict['command_outputs'] += ' --output_dir "$html_file.files_path" --output_html "$html_file" --make_HTML "yes" '
+ xdict['outputs'] += ' \n'
+ if self.opts.output_tab <> 'None':
+ xdict['command_outputs'] += ' --output_tab "$tab_file"'
+ xdict['outputs'] += ' \n' % self.outFormats
+ xdict['command'] = newCommand % xdict
+ xmls = newXML % xdict
+ xf = open(self.xmlfile,'w')
+ xf.write(xmls)
+ xf.write('\n')
+ xf.close()
+ # ready for the tarball
+
+
+ def makeTooltar(self):
+ """
+ a tool is a gz tarball with eg
+ /toolname/tool.xml /toolname/tool.py /toolname/test-data/test1_in.foo ...
+ """
+ retval = self.run()
+ if retval:
+ print >> sys.stderr,'## Run failed. Cannot build yet. Please fix and retry'
+ sys.exit(1)
+ self.makeXML()
+ tdir = self.toolname
+ os.mkdir(tdir)
+ if self.opts.input_tab <> 'None': # no reproducible test otherwise? TODO: maybe..
+ testdir = os.path.join(tdir,'test-data')
+ os.mkdir(testdir) # make tests directory
+ shutil.copyfile(self.opts.input_tab,os.path.join(testdir,self.test1Input))
+ if self.opts.output_tab <> 'None':
+ shutil.copyfile(self.opts.output_tab,os.path.join(testdir,self.test1Output))
+ if self.opts.make_HTML:
+ shutil.copyfile(self.opts.output_html,os.path.join(testdir,self.test1HTML))
+ if self.opts.output_dir:
+ shutil.copyfile(self.tlog,os.path.join(testdir,'test1_out.log'))
+ op = '%s.py' % self.toolname # new name
+ outpiname = os.path.join(tdir,op) # path for the tool tarball
+ pyin = os.path.basename(self.pyfile) # our name - we rewrite ourselves (TM)
+ notes = ['# %s - a self annotated version of %s generated by running %s\n' % (op,pyin,pyin),]
+ notes.append('# to make a new Galaxy tool called %s\n' % self.toolname)
+ notes.append('# User %s at %s\n' % (self.opts.user_email,timenow()))
+ pi = open(self.pyfile,'r').readlines() # our code becomes new tool wrapper (!) - first Galaxy worm
+ notes += pi
+ outpi = open(outpiname,'w')
+ outpi.write(''.join(notes))
+ outpi.write('\n')
+ outpi.close()
+ stname = os.path.join(tdir,self.sfile)
+ if not os.path.exists(stname):
+ shutil.copyfile(self.sfile, stname)
+ xtname = os.path.join(tdir,self.xmlfile)
+ if not os.path.exists(xtname):
+ shutil.copyfile(self.xmlfile,xtname)
+ tarpath = "%s.gz" % self.toolname
+ tar = tarfile.open(tarpath, "w:gz")
+ tar.add(tdir,arcname=self.toolname)
+ tar.close()
+ shutil.copyfile(tarpath,self.opts.new_tool)
+ shutil.rmtree(tdir)
+ ## TODO: replace with optional direct upload to local toolshed?
+ return retval
+
+
+ def compressPDF(self,inpdf=None,thumbformat='png'):
+ """need absolute path to pdf
+ note that GS gets confoozled if no $TMP or $TEMP
+ so we set it
+ """
+ assert os.path.isfile(inpdf), "## Input %s supplied to %s compressPDF not found" % (inpdf,self.myName)
+ our_env = os.environ.copy()
+ if not (our_env.get('TMP',None) or our_env.get('TEMP',None)):
+ our_env['TMP'] = '/tmp'
+ if not self.temp_warned:
+ print >> sys.stdout,'## WARNING - no $TMP or $TEMP!!! Please fix - using /tmp temporarily'
+ self.temp_warned = True
+ hlog = os.path.join(self.opts.output_dir,"compress_%s.txt" % os.path.basename(inpdf))
+ sto = open(hlog,'w')
+ outpdf = '%s_compressed' % inpdf
+ cl = ["gs", "-sDEVICE=pdfwrite", "-dNOPAUSE", "-dBATCH","-dPDFSETTINGS=/printer", "-sOutputFile=%s" % outpdf,inpdf]
+ x = subprocess.Popen(cl,stdout=sto,stderr=sto,cwd=self.opts.output_dir,env=our_env)
+ retval1 = x.wait()
+ sto.close()
+ if retval1 == 0:
+ os.unlink(inpdf)
+ shutil.move(outpdf,inpdf)
+ os.unlink(hlog)
+ else:
+ x = open(hlog,'r').readlines()
+ print >> sys.stdout,x
+ hlog = os.path.join(self.opts.output_dir,"thumbnail_%s.txt" % os.path.basename(inpdf))
+ sto = open(hlog,'w')
+ outpng = '%s.%s' % (os.path.splitext(inpdf)[0],thumbformat)
+ if self.useGM:
+ cl2 = ['gm', 'convert', inpdf, outpng]
+ else: # assume imagemagick
+ cl2 = ['convert', inpdf, outpng]
+ x = subprocess.Popen(cl2,stdout=sto,stderr=sto,cwd=self.opts.output_dir,env=our_env)
+ retval2 = x.wait()
+ sto.close()
+ if retval2 <> 0:
+ x = open(hlog,'r').readlines()
+ print >> sys.stdout,x
+ else:
+ os.unlink(hlog)
+ retval = retval1 or retval2
+ return retval
+
+
+ def getfSize(self,fpath,outpath):
+ """
+ format a nice file size string
+ """
+ size = ''
+ fp = os.path.join(outpath,fpath)
+ if os.path.isfile(fp):
+ size = '0 B'
+ n = float(os.path.getsize(fp))
+ if n > 2**20:
+ size = '%1.1f MB' % (n/2**20)
+ elif n > 2**10:
+ size = '%1.1f KB' % (n/2**10)
+ elif n > 0:
+ size = '%d B' % (int(n))
+ return size
+
+ def makeHtml(self):
+ """ Create an HTML file content to list all the artifacts found in the output_dir
+ """
+
+ galhtmlprefix = """
+
+
+
+
+
+
+
+
+ """
+ galhtmlattr = """
"""
+ galhtmlpostfix = """
\n"""
+
+ flist = os.listdir(self.opts.output_dir)
+ flist = [x for x in flist if x <> 'Rplots.pdf']
+ flist.sort()
+ html = []
+ html.append(galhtmlprefix % progname)
+ html.append('Galaxy Tool "%s" run at %s
' % (self.toolname,timenow()))
+ fhtml = []
+ if len(flist) > 0:
+ logfiles = [x for x in flist if x.lower().endswith('.log')] # log file names determine sections
+ logfiles.sort()
+ logfiles = [x for x in logfiles if os.path.abspath(x) <> os.path.abspath(self.tlog)]
+ logfiles.append(os.path.abspath(self.tlog)) # make it the last one
+ pdflist = []
+ npdf = len([x for x in flist if os.path.splitext(x)[-1].lower() == '.pdf'])
+ for rownum,fname in enumerate(flist):
+ dname,e = os.path.splitext(fname)
+ sfsize = self.getfSize(fname,self.opts.output_dir)
+ if e.lower() == '.pdf' : # compress and make a thumbnail
+ thumb = '%s.%s' % (dname,self.thumbformat)
+ pdff = os.path.join(self.opts.output_dir,fname)
+ retval = self.compressPDF(inpdf=pdff,thumbformat=self.thumbformat)
+ if retval == 0:
+ pdflist.append((fname,thumb))
+ else:
+ pdflist.append((fname,fname))
+ if (rownum+1) % 2 == 0:
+ fhtml.append('%s %s ' % (fname,fname,sfsize))
+ else:
+ fhtml.append('%s %s ' % (fname,fname,sfsize))
+ for logfname in logfiles: # expect at least tlog - if more
+ if os.path.abspath(logfname) == os.path.abspath(self.tlog): # handled later
+ sectionname = 'All tool run'
+ if (len(logfiles) > 1):
+ sectionname = 'Other'
+ ourpdfs = pdflist
+ else:
+ realname = os.path.basename(logfname)
+ sectionname = os.path.splitext(realname)[0].split('_')[0] # break in case _ added to log
+ ourpdfs = [x for x in pdflist if os.path.basename(x[0]).split('_')[0] == sectionname]
+ pdflist = [x for x in pdflist if os.path.basename(x[0]).split('_')[0] <> sectionname] # remove
+ nacross = 1
+ npdf = len(ourpdfs)
+
+ if npdf > 0:
+ nacross = math.sqrt(npdf) ## int(round(math.log(npdf,2)))
+ if int(nacross)**2 != npdf:
+ nacross += 1
+ nacross = int(nacross)
+ width = min(400,int(1200/nacross))
+ html.append('%s images and outputs
' % sectionname)
+ html.append('(Click on a thumbnail image to download the corresponding original PDF image) ')
+ ntogo = nacross # counter for table row padding with empty cells
+ html.append('\n')
+ for i,paths in enumerate(ourpdfs):
+ fname,thumb = paths
+ s= """ \n""" % (fname,thumb,fname,width,fname)
+ if ((i+1) % nacross == 0):
+ s += ' \n'
+ ntogo = 0
+ if i < (npdf - 1): # more to come
+ s += ''
+ ntogo = nacross
+ else:
+ ntogo -= 1
+ html.append(s)
+ if html[-1].strip().endswith(' '):
+ html.append('
\n')
+ else:
+ if ntogo > 0: # pad
+ html.append(' '*ntogo)
+ html.append('\n')
+ logt = open(logfname,'r').readlines()
+ logtext = [x for x in logt if x.strip() > '']
+ html.append('%s log output
' % sectionname)
+ if len(logtext) > 1:
+ html.append('\n\n')
+ html += logtext
+ html.append('\n \n')
+ else:
+ html.append('%s is empty ' % logfname)
+ if len(fhtml) > 0:
+ fhtml.insert(0,'Output File Name (click to view) Size \n')
+ fhtml.append('
')
+ html.append('All output files available for downloading
\n')
+ html += fhtml # add all non-pdf files to the end of the display
+ else:
+ html.append('### Error - %s returned no files - please confirm that parameters are sane
' % self.opts.interpreter)
+ html.append(galhtmlpostfix)
+ htmlf = file(self.opts.output_html,'w')
+ htmlf.write('\n'.join(html))
+ htmlf.write('\n')
+ htmlf.close()
+ self.html = html
+
+
+ def run(self):
+ """
+ scripts must be small enough not to fill the pipe!
+ """
+ if self.treatbashSpecial and self.opts.interpreter in ['bash','sh']:
+ retval = self.runBash()
+ else:
+ if self.opts.output_dir:
+ ste = open(self.elog,'w')
+ sto = open(self.tlog,'w')
+ sto.write('## Toolfactory generated command line = %s\n' % ' '.join(self.cl))
+ sto.flush()
+ p = subprocess.Popen(self.cl,shell=False,stdout=sto,stderr=ste,stdin=subprocess.PIPE,cwd=self.opts.output_dir)
+ else:
+ p = subprocess.Popen(self.cl,shell=False,stdin=subprocess.PIPE)
+ p.stdin.write(self.script)
+ p.stdin.close()
+ retval = p.wait()
+ if self.opts.output_dir:
+ sto.close()
+ ste.close()
+ err = open(self.elog,'r').readlines()
+ if retval <> 0 and err: # problem
+ print >> sys.stderr,err
+ if self.opts.make_HTML:
+ self.makeHtml()
+ return retval
+
+ def runBash(self):
+ """
+ cannot use - for bash so use self.sfile
+ """
+ if self.opts.output_dir:
+ s = '## Toolfactory generated command line = %s\n' % ' '.join(self.cl)
+ sto = open(self.tlog,'w')
+ sto.write(s)
+ sto.flush()
+ p = subprocess.Popen(self.cl,shell=False,stdout=sto,stderr=sto,cwd=self.opts.output_dir)
+ else:
+ p = subprocess.Popen(self.cl,shell=False)
+ retval = p.wait()
+ if self.opts.output_dir:
+ sto.close()
+ if self.opts.make_HTML:
+ self.makeHtml()
+ return retval
+
+
+def main():
+ u = """
+ This is a Galaxy wrapper. It expects to be called by a special purpose tool.xml as:
+ rgBaseScriptWrapper.py --script_path "$scriptPath" --tool_name "foo" --interpreter "Rscript"
+
+ """
+ op = optparse.OptionParser()
+ a = op.add_option
+ a('--script_path',default=None)
+ a('--tool_name',default=None)
+ a('--interpreter',default=None)
+ a('--output_dir',default=None)
+ a('--output_html',default=None)
+ a('--input_tab',default="None")
+ a('--output_tab',default="None")
+ a('--user_email',default='Unknown')
+ a('--bad_user',default=None)
+ a('--make_Tool',default=None)
+ a('--make_HTML',default=None)
+ a('--help_text',default=None)
+ a('--tool_desc',default=None)
+ a('--new_tool',default=None)
+ a('--tool_version',default=None)
+ opts, args = op.parse_args()
+ assert not opts.bad_user,'UNAUTHORISED: %s is NOT authorized to use this tool until Galaxy admin adds %s to admin_users in universe_wsgi.ini' % (opts.bad_user,opts.bad_user)
+ assert opts.tool_name,'## Tool Factory expects a tool name - eg --tool_name=DESeq'
+ assert opts.interpreter,'## Tool Factory wrapper expects an interpreter - eg --interpreter=Rscript'
+ assert os.path.isfile(opts.script_path),'## Tool Factory wrapper expects a script path - eg --script_path=foo.R'
+ if opts.output_dir:
+ try:
+ os.makedirs(opts.output_dir)
+ except:
+ pass
+ r = ScriptRunner(opts)
+ if opts.make_Tool:
+ retcode = r.makeTooltar()
+ else:
+ retcode = r.run()
+ os.unlink(r.sfile)
+ if retcode:
+ sys.exit(retcode) # indicate failure to job runner
+
+
+if __name__ == "__main__":
+ main()
+
+
diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/rgedgeRpaired.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/rgedgeRpaired.xml Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,1084 @@
+
+ models using BioConductor packages
+
+ biocbasics
+ r3
+ graphicsmagick
+ ghostscript
+
+
+
+ rgToolFactory.py --script_path "$runme" --interpreter "Rscript" --tool_name "DifferentialCounts"
+ --output_dir "$html_file.files_path" --output_html "$html_file" --make_HTML "yes"
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Do not run edgeR
+ Run edgeR
+
+
+
+
+
+
+
+
+ Do not run DESeq2
+ Run DESeq2
+
+
+
+ Parametric (default) fit for dispersions
+ Local fit - this will automagically be used if parametric fit fails
+ Mean dispersion fit- use this if you really understand what you're doing - read the fine manual linked below in the documentation
+
+
+
+
+
+ Do not run VOOM
+ Run VOOM
+
+
+
+
+ fdr
+ Benjamini Hochberg
+ Benjamini Yukateli
+ Bonferroni
+ Hochberg
+ Holm
+ Hommel
+ no control for multiple tests
+
+
+
+
+ edgeR['doedgeR'] == "T"
+
+
+ DESeq2['doDESeq2'] == "T"
+
+
+ doVoom == "T"
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ nsamp) {
+ dm =dm[1:nsamp,]
+ #sub = paste('Showing',nsamp,'contigs ranked for evidence for differential abundance out of',nprobes,'total')
+ }
+ newcolnames = substr(colnames(dm),1,20)
+ colnames(dm) = newcolnames
+ pdf(outpdfname)
+ heatmap.2(dm,main=myTitle,ColSideColors=pcols,col=topo.colors(100),dendrogram="col",key=T,density.info='none',
+ Rowv=F,scale='row',trace='none',margins=c(8,8),cexRow=0.4,cexCol=0.5)
+ dev.off()
+}
+
+hmap = function(cmat,nmeans=4,outpdfname="heatMap.pdf",nsamp=250,TName='Treatment',group=NA,myTitle="Title goes here")
+{
+ # for 2 groups only was
+ #col.map = function(g) {if (g==TName) "#FF0000" else "#0000FF"}
+ #pcols = unlist(lapply(group,col.map))
+ gu = unique(group)
+ colours = rainbow(length(gu),start=0.3,end=0.6)
+ pcols = colours[match(group,gu)]
+ nrows = nrow(cmat)
+ mtitle = paste(myTitle,'Heatmap: n contigs =',nrows)
+ if (nrows > nsamp) {
+ cmat = cmat[c(1:nsamp),]
+ mtitle = paste('Heatmap: Top ',nsamp,' DE contigs (of ',nrows,')',sep='')
+ }
+ newcolnames = substr(colnames(cmat),1,20)
+ colnames(cmat) = newcolnames
+ pdf(outpdfname)
+ heatmap(cmat,scale='row',main=mtitle,cexRow=0.3,cexCol=0.4,Rowv=NA,ColSideColors=pcols)
+ dev.off()
+}
+
+qqPlot = function(descr='qqplot',pvector, outpdf='qqplot.pdf',...)
+# stolen from https://gist.github.com/703512
+{
+ o = -log10(sort(pvector,decreasing=F))
+ e = -log10( 1:length(o)/length(o) )
+ o[o==-Inf] = reallysmall
+ o[o==Inf] = reallybig
+ maint = descr
+ pdf(outpdf)
+ plot(e,o,pch=19,cex=1, main=maint, ...,
+ xlab=expression(Expected~~-log[10](italic(p))),
+ ylab=expression(Observed~~-log[10](italic(p))),
+ xlim=c(0,max(e)), ylim=c(0,max(o)))
+ lines(e,e,col="red")
+ grid(col = "lightgray", lty = "dotted")
+ dev.off()
+}
+
+smearPlot = function(DGEList,deTags, outSmear, outMain)
+ {
+ pdf(outSmear)
+ plotSmear(DGEList,de.tags=deTags,main=outMain)
+ grid(col="lightgray", lty="dotted")
+ dev.off()
+ }
+
+boxPlot = function(rawrs,cleanrs,maint,myTitle,pdfname)
+{ #
+ nc = ncol(rawrs)
+ for (i in c(1:nc)) {rawrs[(rawrs[,i] < 0),i] = NA}
+ fullnames = colnames(rawrs)
+ newcolnames = substr(colnames(rawrs),1,20)
+ colnames(rawrs) = newcolnames
+ newcolnames = substr(colnames(cleanrs),1,20)
+ colnames(cleanrs) = newcolnames
+ defpar = par(no.readonly=T)
+ print.noquote('raw contig counts by sample:')
+ print.noquote(summary(rawrs))
+ print.noquote('normalised contig counts by sample:')
+ print.noquote(summary(cleanrs))
+ pdf(pdfname)
+ par(mfrow=c(1,2))
+ boxplot(rawrs,varwidth=T,notch=T,ylab='log contig count',col="maroon",las=3,cex.axis=0.35,main=paste('Raw:',maint))
+ grid(col="lightgray",lty="dotted")
+ boxplot(cleanrs,varwidth=T,notch=T,ylab='log contig count',col="maroon",las=3,cex.axis=0.35,main=paste('After ',maint))
+ grid(col="lightgray",lty="dotted")
+ dev.off()
+ pdfname = "sample_counts_histogram.pdf"
+ nc = ncol(rawrs)
+ print.noquote(paste('Using ncol rawrs=',nc))
+ ncroot = round(sqrt(nc))
+ if (ncroot*ncroot < nc) { ncroot = ncroot + 1 }
+ m = c()
+ for (i in c(1:nc)) {
+ rhist = hist(rawrs[,i],breaks=100,plot=F)
+ m = append(m,max(rhist\$counts))
+ }
+ ymax = max(m)
+ ncols = length(fullnames)
+ if (ncols > 20)
+ {
+ scale = 7*ncols/20
+ pdf(pdfname,width=scale,height=scale)
+ } else {
+ pdf(pdfname)
+ }
+ par(mfrow=c(ncroot,ncroot))
+ for (i in c(1:nc)) {
+ hist(rawrs[,i], main=paste("Contig logcount",i), xlab='log raw count', col="maroon",
+ breaks=100,sub=fullnames[i],cex=0.8,ylim=c(0,ymax))
+ }
+ dev.off()
+ par(defpar)
+
+}
+
+cumPlot = function(rawrs,cleanrs,maint,myTitle)
+{ # updated to use ecdf
+ pdfname = "Filtering_rowsum_bar_charts.pdf"
+ defpar = par(no.readonly=T)
+ lrs = log(rawrs,10)
+ lim = max(lrs)
+ pdf(pdfname)
+ par(mfrow=c(2,1))
+ hist(lrs,breaks=100,main=paste('Before:',maint),xlab="# Reads (log)",
+ ylab="Count",col="maroon",sub=myTitle, xlim=c(0,lim),las=1)
+ grid(col="lightgray", lty="dotted")
+ lrs = log(cleanrs,10)
+ hist(lrs,breaks=100,main=paste('After:',maint),xlab="# Reads (log)",
+ ylab="Count",col="maroon",sub=myTitle,xlim=c(0,lim),las=1)
+ grid(col="lightgray", lty="dotted")
+ dev.off()
+ par(defpar)
+}
+
+cumPlot1 = function(rawrs,cleanrs,maint,myTitle)
+{ # updated to use ecdf
+ pdfname = paste(gsub(" ","", myTitle , fixed=TRUE),"RowsumCum.pdf",sep='_')
+ pdf(pdfname)
+ par(mfrow=c(2,1))
+ lastx = max(rawrs)
+ rawe = knots(ecdf(rawrs))
+ cleane = knots(ecdf(cleanrs))
+ cy = 1:length(cleane)/length(cleane)
+ ry = 1:length(rawe)/length(rawe)
+ plot(rawe,ry,type='l',main=paste('Before',maint),xlab="Log Contig Total Reads",
+ ylab="Cumulative proportion",col="maroon",log='x',xlim=c(1,lastx),sub=myTitle)
+ grid(col="blue")
+ plot(cleane,cy,type='l',main=paste('After',maint),xlab="Log Contig Total Reads",
+ ylab="Cumulative proportion",col="maroon",log='x',xlim=c(1,lastx),sub=myTitle)
+ grid(col="blue")
+ dev.off()
+}
+
+
+
+doGSEAold = function(y=NULL,design=NULL,histgmt="",
+ bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
+ ntest=0, myTitle="myTitle", outfname="GSEA.xls", minnin=5, maxnin=2000,fdrthresh=0.05,fdrtype="BH")
+{
+ sink('Camera.log')
+ genesets = c()
+ if (bigmt > "")
+ {
+ bigenesets = readLines(bigmt)
+ genesets = bigenesets
+ }
+ if (histgmt > "")
+ {
+ hgenesets = readLines(histgmt)
+ if (bigmt > "") {
+ genesets = rbind(genesets,hgenesets)
+ } else {
+ genesets = hgenesets
+ } # use only history if no bi
+ }
+ print.noquote(paste("@@@read",length(genesets), 'genesets from',histgmt,bigmt))
+ genesets = strsplit(genesets,'\t') # tabular. genesetid\tURLorwhatever\tgene_1\t..\tgene_n
+ outf = outfname
+ head=paste(myTitle,'edgeR GSEA')
+ write(head,file=outfname,append=F)
+ ntest=length(genesets)
+ urownames = toupper(rownames(y))
+ upcam = c()
+ downcam = c()
+ for (i in 1:ntest) {
+ gs = unlist(genesets[i])
+ g = gs[1] # geneset_id
+ u = gs[2]
+ if (u > "") { u = paste("",u," ",sep="") }
+ glist = gs[3:length(gs)] # member gene symbols
+ glist = toupper(glist)
+ inglist = urownames %in% glist
+ nin = sum(inglist)
+ if ((nin > minnin) && (nin < maxnin)) {
+ ### print(paste('@@found',sum(inglist),'genes in glist'))
+ camres = camera(y=y,index=inglist,design=design)
+ if (! is.null(camres)) {
+ rownames(camres) = g # gene set name
+ camres = cbind(GeneSet=g,URL=u,camres)
+ if (camres\$Direction == "Up")
+ {
+ upcam = rbind(upcam,camres) } else {
+ downcam = rbind(downcam,camres)
+ }
+ }
+ }
+ }
+ uscam = upcam[order(upcam\$PValue),]
+ unadjp = uscam\$PValue
+ uscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ nup = max(10,sum((uscam\$adjPValue < fdrthresh)))
+ dscam = downcam[order(downcam\$PValue),]
+ unadjp = dscam\$PValue
+ dscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ ndown = max(10,sum((dscam\$adjPValue < fdrthresh)))
+ write.table(uscam,file=paste('camera_up',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ write.table(dscam,file=paste('camera_down',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera up top',nup,'gene sets:'))
+ write.table(head(uscam,nup),file="",quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera down top',ndown,'gene sets:'))
+ write.table(head(dscam,ndown),file="",quote=F,sep='\t',row.names=F)
+ sink()
+}
+
+
+
+
+doGSEA = function(y=NULL,design=NULL,histgmt="",
+ bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
+ ntest=0, myTitle="myTitle", outfname="GSEA.xls", minnin=5, maxnin=2000,fdrthresh=0.05,fdrtype="BH")
+{
+ sink('Camera.log')
+ genesets = c()
+ if (bigmt > "")
+ {
+ bigenesets = readLines(bigmt)
+ genesets = bigenesets
+ }
+ if (histgmt > "")
+ {
+ hgenesets = readLines(histgmt)
+ if (bigmt > "") {
+ genesets = rbind(genesets,hgenesets)
+ } else {
+ genesets = hgenesets
+ } # use only history if no bi
+ }
+ print.noquote(paste("@@@read",length(genesets), 'genesets from',histgmt,bigmt))
+ genesets = strsplit(genesets,'\t') # tabular. genesetid\tURLorwhatever\tgene_1\t..\tgene_n
+ outf = outfname
+ head=paste(myTitle,'edgeR GSEA')
+ write(head,file=outfname,append=F)
+ ntest=length(genesets)
+ urownames = toupper(rownames(y))
+ upcam = c()
+ downcam = c()
+ incam = c()
+ urls = c()
+ gsids = c()
+ for (i in 1:ntest) {
+ gs = unlist(genesets[i])
+ gsid = gs[1] # geneset_id
+ url = gs[2]
+ if (url > "") { url = paste("",url," ",sep="") }
+ glist = gs[3:length(gs)] # member gene symbols
+ glist = toupper(glist)
+ inglist = urownames %in% glist
+ nin = sum(inglist)
+ if ((nin > minnin) && (nin < maxnin)) {
+ incam = c(incam,inglist)
+ gsids = c(gsids,gsid)
+ urls = c(urls,url)
+ }
+ }
+ incam = as.list(incam)
+ names(incam) = gsids
+ allcam = camera(y=y,index=incam,design=design)
+ allcamres = cbind(geneset=gsids,allcam,URL=urls)
+ for (i in 1:ntest) {
+ camres = allcamres[i]
+ res = try(test = (camres\$Direction == "Up"))
+ if ("try-error" %in% class(res)) {
+ cat("test failed, camres = :")
+ print.noquote(camres)
+ } else { if (camres\$Direction == "Up")
+ { upcam = rbind(upcam,camres)
+ } else { downcam = rbind(downcam,camres)
+ }
+
+ }
+ }
+ uscam = upcam[order(upcam\$PValue),]
+ unadjp = uscam\$PValue
+ uscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ nup = max(10,sum((uscam\$adjPValue < fdrthresh)))
+ dscam = downcam[order(downcam\$PValue),]
+ unadjp = dscam\$PValue
+ dscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ ndown = max(10,sum((dscam\$adjPValue < fdrthresh)))
+ write.table(uscam,file=paste('camera_up',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ write.table(dscam,file=paste('camera_down',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera up top',nup,'gene sets:'))
+ write.table(head(uscam,nup),file="",quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera down top',ndown,'gene sets:'))
+ write.table(head(dscam,ndown),file="",quote=F,sep='\t',row.names=F)
+ sink()
+ }
+
+
+edgeIt = function (Count_Matrix=c(),group=c(),out_edgeR=F,out_VOOM=F,out_DESeq2=F,fdrtype='fdr',priordf=5,
+ fdrthresh=0.05,outputdir='.', myTitle='Differential Counts',libSize=c(),useNDF=F,
+ filterquantile=0.2, subjects=c(),mydesign=NULL,
+ doDESeq2=T,doVoom=T,doCamera=T,doedgeR=T,org='hg19',
+ histgmt="", bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
+ doCook=F,DESeq_fitType="parameteric")
+{
+ # Error handling
+ if (length(unique(group))!=2){
+ print("Number of conditions identified in experiment does not equal 2")
+ q()
+ }
+ require(edgeR)
+ options(width = 512)
+ mt = paste(unlist(strsplit(myTitle,'_')),collapse=" ")
+ allN = nrow(Count_Matrix)
+ nscut = round(ncol(Count_Matrix)/2)
+ colTotmillionreads = colSums(Count_Matrix)/1e6
+ counts.dataframe = as.data.frame(c())
+ rawrs = rowSums(Count_Matrix)
+ nonzerod = Count_Matrix[(rawrs > 0),] # remove all zero count genes
+ nzN = nrow(nonzerod)
+ nzrs = rowSums(nonzerod)
+ zN = allN - nzN
+ print('# Quantiles for non-zero row counts:',quote=F)
+ print(quantile(nzrs,probs=seq(0,1,0.1)),quote=F)
+ if (useNDF == T)
+ {
+ gt1rpin3 = rowSums(Count_Matrix/expandAsMatrix(colTotmillionreads,dim(Count_Matrix)) >= 1) >= nscut
+ lo = colSums(Count_Matrix[!gt1rpin3,])
+ workCM = Count_Matrix[gt1rpin3,]
+ cleanrs = rowSums(workCM)
+ cleanN = length(cleanrs)
+ meth = paste( "After removing",length(lo),"contigs with fewer than ",nscut," sample read counts >= 1 per million, there are",sep="")
+ print(paste("Read",allN,"contigs. Removed",zN,"contigs with no reads.",meth,cleanN,"contigs"),quote=F)
+ maint = paste('Filter >=1/million reads in >=',nscut,'samples')
+ } else {
+ useme = (nzrs > quantile(nzrs,filterquantile))
+ workCM = nonzerod[useme,]
+ lo = colSums(nonzerod[!useme,])
+ cleanrs = rowSums(workCM)
+ cleanN = length(cleanrs)
+ meth = paste("After filtering at count quantile =",filterquantile,", there are",sep="")
+ print(paste('Read',allN,"contigs. Removed",zN,"with no reads.",meth,cleanN,"contigs"),quote=F)
+ maint = paste('Filter below',filterquantile,'quantile')
+ }
+ cumPlot(rawrs=rawrs,cleanrs=cleanrs,maint=maint,myTitle=myTitle)
+ allgenes = rownames(workCM)
+ reg = "^chr([0-9]+):([0-9]+)-([0-9]+)"
+ genecards=" 0.8) # is ucsc style string
+ {
+ print("@@ using ucsc substitution for urls")
+ contigurls = paste0(ucsc,"&position=chr",testreg[,2],":",testreg[,3],"-",testreg[,4],"\'>",allgenes," ")
+ } else {
+ print("@@ using genecards substitution for urls")
+ contigurls = paste0(genecards,allgenes,"\'>",allgenes,"")
+ }
+ print.noquote("# urls")
+ print.noquote(head(contigurls))
+ print(paste("# Total low count contigs per sample = ",paste(lo,collapse=',')),quote=F)
+ cmrowsums = rowSums(workCM)
+ TName=unique(group)[1]
+ CName=unique(group)[2]
+ if (is.null(mydesign)) {
+ if (length(subjects) == 0)
+ {
+ mydesign = model.matrix(~group)
+ }
+ else {
+ subjf = factor(subjects)
+ mydesign = model.matrix(~subjf+group) # we block on subject so make group last to simplify finding it
+ }
+ }
+ print.noquote(paste('Using samples:',paste(colnames(workCM),collapse=',')))
+ print.noquote('Using design matrix:')
+ print.noquote(mydesign)
+ if (doedgeR) {
+ sink('edgeR.log')
+ #### Setup DGEList object
+ DGEList = DGEList(counts=workCM, group = group)
+ DGEList = calcNormFactors(DGEList)
+
+ DGEList = estimateGLMCommonDisp(DGEList,mydesign)
+ comdisp = DGEList\$common.dispersion
+ DGEList = estimateGLMTrendedDisp(DGEList,mydesign)
+ if (edgeR_priordf > 0) {
+ print.noquote(paste("prior.df =",edgeR_priordf))
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign,prior.df = edgeR_priordf)
+ } else {
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
+ }
+ DGLM = glmFit(DGEList,design=mydesign)
+ DE = glmLRT(DGLM,coef=ncol(DGLM\$design)) # always last one - subject is first if needed
+ efflib = DGEList\$samples\$lib.size*DGEList\$samples\$norm.factors
+ normData = (1e+06*DGEList\$counts/efflib)
+ uoutput = cbind(
+ Name=as.character(rownames(DGEList\$counts)),
+ DE\$table,
+ adj.p.value=p.adjust(DE\$table\$PValue, method=fdrtype),
+ Dispersion=DGEList\$tagwise.dispersion,totreads=cmrowsums,normData,
+ DGEList\$counts
+ )
+ soutput = uoutput[order(DE\$table\$PValue),] # sorted into p value order - for quick toptable
+ goodness = gof(DGLM, pcutoff=fdrthresh)
+ if (sum(goodness\$outlier) > 0) {
+ print.noquote('GLM outliers:')
+ print(paste(rownames(DGLM)[(goodness\$outlier)],collapse=','),quote=F)
+ } else {
+ print('No GLM fit outlier genes found\n')
+ }
+ z = limma::zscoreGamma(goodness\$gof.statistic, shape=goodness\$df/2, scale=2)
+ pdf("edgeR_GoodnessofFit.pdf")
+ qq = qqnorm(z, panel.first=grid(), main="tagwise dispersion")
+ abline(0,1,lwd=3)
+ points(qq\$x[goodness\$outlier],qq\$y[goodness\$outlier], pch=16, col="maroon")
+ dev.off()
+ estpriorn = getPriorN(DGEList)
+ print(paste("Common Dispersion =",comdisp,"CV = ",sqrt(comdisp),"getPriorN = ",estpriorn),quote=F)
+ efflib = DGEList\$samples\$lib.size*DGEList\$samples\$norm.factors
+ normData = (1e+06*DGEList\$counts/efflib)
+ uniqueg = unique(group)
+ #### Plot MDS
+ sample_colors = match(group,levels(group))
+ sampleTypes = levels(factor(group))
+ print.noquote(sampleTypes)
+ pdf("edgeR_MDSplot.pdf")
+ plotMDS.DGEList(DGEList,main=paste("edgeR MDS for",myTitle),cex=0.5,col=sample_colors,pch=sample_colors)
+ legend(x="topleft", legend = sampleTypes,col=c(1:length(sampleTypes)), pch=19)
+ grid(col="blue")
+ dev.off()
+ colnames(normData) = paste( colnames(normData),'N',sep="_")
+ print(paste('Raw sample read totals',paste(colSums(nonzerod,na.rm=T),collapse=',')))
+ nzd = data.frame(log(nonzerod + 1e-2,10))
+ try( boxPlot(rawrs=nzd,cleanrs=log(normData,10),maint='TMM Normalisation',myTitle=myTitle,pdfname="edgeR_raw_norm_counts_box.pdf") )
+ write.table(soutput,file=out_edgeR, quote=FALSE, sep="\t",row.names=F)
+ tt = cbind(
+ Name=as.character(rownames(DGEList\$counts)),
+ DE\$table,
+ adj.p.value=p.adjust(DE\$table\$PValue, method=fdrtype),
+ Dispersion=DGEList\$tagwise.dispersion,totreads=cmrowsums
+ )
+ print.noquote("# edgeR Top tags\n")
+ tt = cbind(tt,URL=contigurls) # add to end so table isn't laid out strangely
+ tt = tt[order(DE\$table\$PValue),]
+ print.noquote(tt[1:50,])
+ deTags = rownames(uoutput[uoutput\$adj.p.value < fdrthresh,])
+ nsig = length(deTags)
+ print(paste('#',nsig,'tags significant at adj p=',fdrthresh),quote=F)
+ deColours = ifelse(deTags,'red','black')
+ pdf("edgeR_BCV_vs_abundance.pdf")
+ plotBCV(DGEList, cex=0.3, main="Biological CV vs abundance")
+ dev.off()
+ dg = DGEList[order(DE\$table\$PValue),]
+ #normData = (1e+06 * dg\$counts/expandAsMatrix(dg\$samples\$lib.size, dim(dg)))
+ efflib = dg\$samples\$lib.size*dg\$samples\$norm.factors
+ normData = (1e+06*dg\$counts/efflib)
+ outpdfname="edgeR_top_100_heatmap.pdf"
+ hmap2(normData,nsamp=100,TName=TName,group=group,outpdfname=outpdfname,myTitle=paste('edgeR Heatmap',myTitle))
+ outSmear = "edgeR_smearplot.pdf"
+ outMain = paste("Smear Plot for ",TName,' Vs ',CName,' (FDR@',fdrthresh,' N = ',nsig,')',sep='')
+ smearPlot(DGEList=DGEList,deTags=deTags, outSmear=outSmear, outMain = outMain)
+ qqPlot(descr=paste(myTitle,'edgeR adj p QQ plot'),pvector=tt\$adj.p.value,outpdf='edgeR_qqplot.pdf')
+ norm.factor = DGEList\$samples\$norm.factors
+ topresults.edgeR = soutput[which(soutput\$adj.p.value < fdrthresh), ]
+ edgeRcountsindex = which(allgenes %in% rownames(topresults.edgeR))
+ edgeRcounts = rep(0, length(allgenes))
+ edgeRcounts[edgeRcountsindex] = 1 # Create venn diagram of hits
+ sink()
+ } ### doedgeR
+ if (doDESeq2 == T)
+ {
+ sink("DESeq2.log")
+ # DESeq2
+ require('DESeq2')
+ library('RColorBrewer')
+ if (length(subjects) == 0)
+ {
+ pdata = data.frame(Name=colnames(workCM),Rx=group,row.names=colnames(workCM))
+ deSEQds = DESeqDataSetFromMatrix(countData = workCM, colData = pdata, design = formula(~ Rx))
+ } else {
+ pdata = data.frame(Name=colnames(workCM),Rx=group,subjects=subjects,row.names=colnames(workCM))
+ deSEQds = DESeqDataSetFromMatrix(countData = workCM, colData = pdata, design = formula(~ subjects + Rx))
+ }
+ #DESeq2 = DESeq(deSEQds,fitType='local',pAdjustMethod=fdrtype)
+ #rDESeq = results(DESeq2)
+ #newCountDataSet(workCM, group)
+ deSeqDatsizefac = estimateSizeFactors(deSEQds)
+ deSeqDatdisp = estimateDispersions(deSeqDatsizefac,fitType=DESeq_fitType)
+ resDESeq = nbinomWaldTest(deSeqDatdisp, pAdjustMethod=fdrtype)
+ rDESeq = as.data.frame(results(resDESeq))
+ rDESeq = cbind(Contig=rownames(workCM),rDESeq,NReads=cmrowsums,URL=contigurls)
+ srDESeq = rDESeq[order(rDESeq\$pvalue),]
+ qqPlot(descr=paste(myTitle,'DESeq2 adj p qq plot'),pvector=rDESeq\$padj,outpdf='DESeq2_qqplot.pdf')
+ cat("# DESeq top 50\n")
+ print.noquote(srDESeq[1:50,])
+ write.table(srDESeq,file=out_DESeq2, quote=FALSE, sep="\t",row.names=F)
+ topresults.DESeq = rDESeq[which(rDESeq\$padj < fdrthresh), ]
+ DESeqcountsindex = which(allgenes %in% rownames(topresults.DESeq))
+ DESeqcounts = rep(0, length(allgenes))
+ DESeqcounts[DESeqcountsindex] = 1
+ pdf("DESeq2_dispersion_estimates.pdf")
+ plotDispEsts(resDESeq)
+ dev.off()
+ ysmall = abs(min(rDESeq\$log2FoldChange))
+ ybig = abs(max(rDESeq\$log2FoldChange))
+ ylimit = min(4,ysmall,ybig)
+ pdf("DESeq2_MA_plot.pdf")
+ plotMA(resDESeq,main=paste(myTitle,"DESeq2 MA plot"),ylim=c(-ylimit,ylimit))
+ dev.off()
+ rlogres = rlogTransformation(resDESeq)
+ sampledists = dist( t( assay(rlogres) ) )
+ sdmat = as.matrix(sampledists)
+ pdf("DESeq2_sample_distance_plot.pdf")
+ heatmap.2(sdmat,trace="none",main=paste(myTitle,"DESeq2 sample distances"),
+ col = colorRampPalette( rev(brewer.pal(9, "RdBu")) )(255))
+ dev.off()
+ ###outpdfname="DESeq2_top50_heatmap.pdf"
+ ###hmap2(sresDESeq,nsamp=50,TName=TName,group=group,outpdfname=outpdfname,myTitle=paste('DESeq2 vst rlog Heatmap',myTitle))
+ sink()
+ result = try( (ppca = plotPCA( varianceStabilizingTransformation(deSeqDatdisp,blind=T), intgroup=c("Rx","Name")) ) )
+ if ("try-error" %in% class(result)) {
+ print.noquote('DESeq2 plotPCA failed.')
+ } else {
+ pdf("DESeq2_PCA_plot.pdf")
+ #### wtf - print? Seems needed to get this to work
+ print(ppca)
+ dev.off()
+ }
+ }
+
+ if (doVoom == T) {
+ sink('VOOM.log')
+ if (doedgeR == F) {
+ #### Setup DGEList object
+ DGEList = DGEList(counts=workCM, group = group)
+ DGEList = calcNormFactors(DGEList)
+ DGEList = estimateGLMCommonDisp(DGEList,mydesign)
+ DGEList = estimateGLMTrendedDisp(DGEList,mydesign)
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
+ norm.factor = DGEList\$samples\$norm.factors
+ }
+ pdf("VOOM_mean_variance_plot.pdf")
+ dat.voomed = voom(DGEList, mydesign, plot = TRUE, lib.size = colSums(workCM) * norm.factor)
+ dev.off()
+ # Use limma to fit data
+ fit = lmFit(dat.voomed, mydesign)
+ fit = eBayes(fit)
+ rvoom = topTable(fit, coef = length(colnames(mydesign)), adj = fdrtype, n = Inf, sort="none")
+ qqPlot(descr=paste(myTitle,'VOOM-limma adj p QQ plot'),pvector=rvoom\$adj.P.Val,outpdf='VOOM_qqplot.pdf')
+ rownames(rvoom) = rownames(workCM)
+ rvoom = cbind(rvoom,NReads=cmrowsums,URL=contigurls)
+ srvoom = rvoom[order(rvoom\$P.Value),]
+ cat("# VOOM top 50\n")
+ print(srvoom[1:50,])
+ write.table(srvoom,file=out_VOOM, quote=FALSE, sep="\t",row.names=F)
+ # Use an FDR cutoff to find interesting samples for edgeR, DESeq and voom/limma
+ topresults.voom = rvoom[which(rvoom\$adj.P.Val < fdrthresh), ]
+ voomcountsindex = which(allgenes %in% topresults.voom\$ID)
+ voomcounts = rep(0, length(allgenes))
+ voomcounts[voomcountsindex] = 1
+ sink()
+ }
+
+ if (doCamera) {
+ doGSEA(y=DGEList,design=mydesign,histgmt=histgmt,bigmt=bigmt,ntest=20,myTitle=myTitle,
+ outfname=paste(mt,"GSEA.xls",sep="_"),fdrthresh=fdrthresh,fdrtype=fdrtype)
+ }
+
+ if ((doDESeq2==T) || (doVoom==T) || (doedgeR==T)) {
+ if ((doVoom==T) && (doDESeq2==T) && (doedgeR==T)) {
+ vennmain = paste(mt,'Voom,edgeR and DESeq2 overlap at FDR=',fdrthresh)
+ counts.dataframe = data.frame(edgeR = edgeRcounts, DESeq2 = DESeqcounts,
+ VOOM_limma = voomcounts, row.names = allgenes)
+ } else if ((doDESeq2==T) && (doedgeR==T)) {
+ vennmain = paste(mt,'DESeq2 and edgeR overlap at FDR=',fdrthresh)
+ counts.dataframe = data.frame(edgeR = edgeRcounts, DESeq2 = DESeqcounts, row.names = allgenes)
+ } else if ((doVoom==T) && (doedgeR==T)) {
+ vennmain = paste(mt,'Voom and edgeR overlap at FDR=',fdrthresh)
+ counts.dataframe = data.frame(edgeR = edgeRcounts, VOOM_limma = voomcounts, row.names = allgenes)
+ }
+
+ if (nrow(counts.dataframe > 1)) {
+ counts.venn = vennCounts(counts.dataframe)
+ vennf = "Venn_significant_genes_overlap.pdf"
+ pdf(vennf)
+ vennDiagram(counts.venn,main=vennmain,col="maroon")
+ dev.off()
+ }
+ } #### doDESeq2 or doVoom
+
+}
+#### Done
+
+###sink(stdout(),append=T,type="message")
+builtin_gmt = ""
+history_gmt = ""
+history_gmt_name = ""
+out_edgeR = F
+out_DESeq2 = F
+out_VOOM = "$out_VOOM"
+doDESeq2 = $DESeq2.doDESeq2 # make these T or F
+doVoom = $doVoom
+doCamera = F
+doedgeR = $edgeR.doedgeR
+edgeR_priordf = 0
+
+
+#if $doVoom == "T":
+ out_VOOM = "$out_VOOM"
+#end if
+
+#if $DESeq2.doDESeq2 == "T":
+ out_DESeq2 = "$out_DESeq2"
+ DESeq_fitType = "$DESeq2.DESeq_fitType"
+#end if
+
+#if $edgeR.doedgeR == "T":
+ out_edgeR = "$out_edgeR"
+ edgeR_priordf = $edgeR.edgeR_priordf
+#end if
+
+
+
+if (sum(c(doedgeR,doVoom,doDESeq2)) == 0)
+{
+write("No methods chosen - nothing to do! Please try again after choosing one or more methods", stderr())
+quit(save="no",status=2)
+}
+
+Out_Dir = "$html_file.files_path"
+Input = "$input1"
+TreatmentName = "$treatment_name"
+TreatmentCols = "$Treat_cols"
+ControlName = "$control_name"
+ControlCols= "$Control_cols"
+org = "$input1.dbkey"
+if (org == "") { org = "hg19"}
+fdrtype = "$fdrtype"
+fdrthresh = $fdrthresh
+useNDF = $useNDF
+fQ = $fQ # non-differential centile cutoff
+myTitle = "$title"
+sids = strsplit("$subjectids",',')
+subjects = unlist(sids)
+nsubj = length(subjects)
+TCols = as.numeric(strsplit(TreatmentCols,",")[[1]])-1
+CCols = as.numeric(strsplit(ControlCols,",")[[1]])-1
+cat('Got TCols=')
+cat(TCols)
+cat('; CCols=')
+cat(CCols)
+cat('\n')
+useCols = c(TCols,CCols)
+if (file.exists(Out_Dir) == F) dir.create(Out_Dir)
+Count_Matrix = read.table(Input,header=T,row.names=1,sep='\t') #Load tab file assume header
+snames = colnames(Count_Matrix)
+nsamples = length(snames)
+if (nsubj > 0 & nsubj != nsamples) {
+options("show.error.messages"=T)
+mess = paste('Fatal error: Supplied subject id list',paste(subjects,collapse=','),
+ 'has length',nsubj,'but there are',nsamples,'samples',paste(snames,collapse=','))
+write(mess, stderr())
+quit(save="no",status=4)
+}
+if (length(subjects) != 0) {subjects = subjects[useCols]}
+Count_Matrix = Count_Matrix[,useCols] ### reorder columns
+rn = rownames(Count_Matrix)
+islib = rn %in% c('librarySize','NotInBedRegions')
+LibSizes = Count_Matrix[subset(rn,islib),][1] # take first
+Count_Matrix = Count_Matrix[subset(rn,! islib),]
+group = c(rep(TreatmentName,length(TCols)), rep(ControlName,length(CCols)) ) #Build a group descriptor
+group = factor(group, levels=c(ControlName,TreatmentName))
+colnames(Count_Matrix) = paste(group,colnames(Count_Matrix),sep="_") #Relable columns
+results = edgeIt(Count_Matrix=Count_Matrix,group=group, out_edgeR=out_edgeR, out_VOOM=out_VOOM, out_DESeq2=out_DESeq2,
+ fdrtype='BH',mydesign=NULL,priordf=edgeR_priordf,fdrthresh=fdrthresh,outputdir='.',
+ myTitle=myTitle,useNDF=F,libSize=c(),filterquantile=fQ,subjects=subjects,
+ doDESeq2=doDESeq2,doVoom=doVoom,doCamera=doCamera,doedgeR=doedgeR,org=org,
+ histgmt=history_gmt,bigmt=builtin_gmt,DESeq_fitType=DESeq_fitType)
+sessionInfo()
+]]>
+
+
+
+
+**What it does**
+
+Allows short read sequence counts from controlled experiments to be analysed for differentially expressed genes.
+Optionally adds a term for subject if not all samples are independent or if some other factor needs to be blocked in the design.
+
+**Input**
+
+Requires a count matrix as a tabular file. These are best made using the companion HTSeq_ based counter Galaxy wrapper
+and your fave gene model to generate inputs. Each row is a genomic feature (gene or exon eg) and each column the
+non-negative integer count of reads from one sample overlapping the feature.
+The matrix must have a header row uniquely identifying the source samples, and unique row names in
+the first column. Typically the row names are gene symbols or probe ids for downstream use in GSEA and other methods.
+
+**Specifying comparisons**
+
+This is basically dumbed down for two factors - case vs control.
+
+More complex interfaces are possible but painful at present.
+Probably need to specify a phenotype file to do this better.
+Work in progress. Send code.
+
+If you have (eg) paired samples and wish to include a term in the GLM to account for some other factor (subject in the case of paired samples),
+put a comma separated list of indicators for every sample (whether modelled or not!) indicating (eg) the subject number or
+A list of integers, one for each subject or an empty string if samples are all independent.
+If not empty, there must be exactly as many integers in the supplied integer list as there are columns (samples) in the count matrix.
+Integers for samples that are not in the analysis *must* be present in the string as filler even if not used.
+
+So if you have 2 pairs out of 6 samples, you need to put in unique integers for the unpaired ones
+eg if you had 6 samples with the first two independent but the second and third pairs each being from independent subjects. you might use
+8,9,1,1,2,2
+as subject IDs to indicate two paired samples from the same subject in columns 3/4 and 5/6
+
+**Methods available**
+
+You can run 3 popular Bioconductor packages available for count data.
+
+edgeR - see edgeR_ for details
+
+VOOM/limma - see limma_VOOM_ for details
+
+DESeq2 - see DESeq2_ for details
+
+and optionally camera in edgeR which works better if MSigDB is installed.
+
+**Outputs**
+
+Some helpful plots and analysis results. Note that most of these are produced using R code
+suggested by the excellent documentation and vignettes for the Bioconductor
+packages invoked. The Tool Factory is used to automatically lay these out for you to enjoy.
+
+**Note on Voom**
+
+The voom from limma version 3.16.6 help in R includes this from the authors - but you should read the paper to interpret this method.
+
+This function is intended to process RNA-Seq or ChIP-Seq data prior to linear modelling in limma.
+
+voom is an acronym for mean-variance modelling at the observational level.
+The key concern is to estimate the mean-variance relationship in the data, then use this to compute appropriate weights for each observation.
+Count data almost show non-trivial mean-variance relationships. Raw counts show increasing variance with increasing count size, while log-counts typically show a decreasing mean-variance trend.
+This function estimates the mean-variance trend for log-counts, then assigns a weight to each observation based on its predicted variance.
+The weights are then used in the linear modelling process to adjust for heteroscedasticity.
+
+In an experiment, a count value is observed for each tag in each sample. A tag-wise mean-variance trend is computed using lowess.
+The tag-wise mean is the mean log2 count with an offset of 0.5, across samples for a given tag.
+The tag-wise variance is the quarter-root-variance of normalized log2 counts per million values with an offset of 0.5, across samples for a given tag.
+Tags with zero counts across all samples are not included in the lowess fit. Optional normalization is performed using normalizeBetweenArrays.
+Using fitted values of log2 counts from a linear model fit by lmFit, variances from the mean-variance trend were interpolated for each observation.
+This was carried out by approxfun. Inverse variance weights can be used to correct for mean-variance trend in the count data.
+
+
+Author(s)
+
+Charity Law and Gordon Smyth
+
+References
+
+Law, CW (2013). Precision weights for gene expression analysis. PhD Thesis. University of Melbourne, Australia.
+
+Law, CW, Chen, Y, Shi, W, Smyth, GK (2013). Voom! Precision weights unlock linear model analysis tools for RNA-seq read counts.
+Technical Report 1 May 2013, Bioinformatics Division, Walter and Eliza Hall Institute of Medical Reseach, Melbourne, Australia.
+http://www.statsci.org/smyth/pubs/VoomPreprint.pdf
+
+See Also
+
+A voom case study is given in the edgeR User's Guide.
+
+vooma is a similar function but for microarrays instead of RNA-seq.
+
+
+***old rant on changes to Bioconductor package variable names between versions***
+
+The edgeR authors made a small cosmetic change in the name of one important variable (from p.value to PValue)
+breaking this and all other code that assumed the old name for this variable,
+between edgeR2.4.4 and 2.4.6 (the version for R 2.14 as at the time of writing).
+This means that all code using edgeR is sensitive to the version. I think this was a very unwise thing
+to do because it wasted hours of my time to track down and will similarly cost other edgeR users dearly
+when their old scripts break. This tool currently now works with 2.4.6.
+
+**Note on prior.N**
+
+http://seqanswers.com/forums/showthread.php?t=5591 says:
+
+*prior.n*
+
+The value for prior.n determines the amount of smoothing of tagwise dispersions towards the common dispersion.
+You can think of it as like a "weight" for the common value. (It is actually the weight for the common likelihood
+in the weighted likelihood equation). The larger the value for prior.n, the more smoothing, i.e. the closer your
+tagwise dispersion estimates will be to the common dispersion. If you use a prior.n of 1, then that gives the
+common likelihood the weight of one observation.
+
+In answer to your question, it is a good thing to squeeze the tagwise dispersions towards a common value,
+or else you will be using very unreliable estimates of the dispersion. I would not recommend using the value that
+you obtained from estimateSmoothing()---this is far too small and would result in virtually no moderation
+(squeezing) of the tagwise dispersions. How many samples do you have in your experiment?
+What is the experimental design? If you have few samples (less than 6) then I would suggest a prior.n of at least 10.
+If you have more samples, then the tagwise dispersion estimates will be more reliable,
+so you could consider using a smaller prior.n, although I would hesitate to use a prior.n less than 5.
+
+
+From Bioconductor Digest, Vol 118, Issue 5, Gordon writes:
+
+Dear Dorota,
+
+The important settings are prior.df and trend.
+
+prior.n and prior.df are related through prior.df = prior.n * residual.df,
+and your experiment has residual.df = 36 - 12 = 24. So the old setting of
+prior.n=10 is equivalent for your data to prior.df = 240, a very large
+value. Going the other way, the new setting of prior.df=10 is equivalent
+to prior.n=10/24.
+
+To recover old results with the current software you would use
+
+ estimateTagwiseDisp(object, prior.df=240, trend="none")
+
+To get the new default from old software you would use
+
+ estimateTagwiseDisp(object, prior.n=10/24, trend=TRUE)
+
+Actually the old trend method is equivalent to trend="loess" in the new
+software. You should use plotBCV(object) to see whether a trend is
+required.
+
+Note you could also use
+
+ prior.n = getPriorN(object, prior.df=10)
+
+to map between prior.df and prior.n.
+
+----
+
+**Attributions**
+
+edgeR - edgeR_
+
+VOOM/limma - limma_VOOM_
+
+DESeq2 - DESeq2_ for details
+
+See above for Bioconductor package documentation for packages exposed in Galaxy by this tool and app store package.
+
+Galaxy_ (that's what you are using right now!) for gluing everything together
+
+Otherwise, all code and documentation comprising this tool was written by Ross Lazarus and is
+licensed to you under the LGPL_ like other rgenetics artefacts
+
+.. _LGPL: http://www.gnu.org/copyleft/lesser.html
+.. _HTSeq: http://www-huber.embl.de/users/anders/HTSeq/doc/index.html
+.. _edgeR: http://www.bioconductor.org/packages/release/bioc/html/edgeR.html
+.. _DESeq2: http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html
+.. _limma_VOOM: http://www.bioconductor.org/packages/release/bioc/html/limma.html
+.. _Galaxy: http://getgalaxy.org
+
+
+
+
+
diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/rgedgeRpaired_nocamera.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/rgedgeRpaired_nocamera.xml Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,1072 @@
+
+ models using BioConductor packages
+
+ biocbasics
+ r3
+ graphicsmagick
+ ghostscript
+
+
+
+ rgToolFactory.py --script_path "$runme" --interpreter "Rscript" --tool_name "DifferentialCounts"
+ --output_dir "$html_file.files_path" --output_html "$html_file" --make_HTML "yes"
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ Do not run edgeR
+ Run edgeR
+
+
+
+
+
+
+
+
+ Do not run DESeq2
+ Run DESeq2
+
+
+
+ Parametric (default) fit for dispersions
+ Local fit - this will automagically be used if parametric fit fails
+ Mean dispersion fit- use this if you really understand what you're doing - read the fine manual linked below in the documentation
+
+
+
+
+
+ Do not run VOOM
+ Run VOOM
+
+
+
+
+ fdr
+ Benjamini Hochberg
+ Benjamini Yukateli
+ Bonferroni
+ Hochberg
+ Holm
+ Hommel
+ no control for multiple tests
+
+
+
+
+ edgeR['doedgeR'] == "T"
+
+
+ DESeq2['doDESeq2'] == "T"
+
+
+ doVoom == "T"
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ nsamp) {
+ dm =dm[1:nsamp,]
+ #sub = paste('Showing',nsamp,'contigs ranked for evidence for differential abundance out of',nprobes,'total')
+ }
+ newcolnames = substr(colnames(dm),1,20)
+ colnames(dm) = newcolnames
+ pdf(outpdfname)
+ heatmap.2(dm,main=myTitle,ColSideColors=pcols,col=topo.colors(100),dendrogram="col",key=T,density.info='none',
+ Rowv=F,scale='row',trace='none',margins=c(8,8),cexRow=0.4,cexCol=0.5)
+ dev.off()
+}
+
+hmap = function(cmat,nmeans=4,outpdfname="heatMap.pdf",nsamp=250,TName='Treatment',group=NA,myTitle="Title goes here")
+{
+ # for 2 groups only was
+ #col.map = function(g) {if (g==TName) "#FF0000" else "#0000FF"}
+ #pcols = unlist(lapply(group,col.map))
+ gu = unique(group)
+ colours = rainbow(length(gu),start=0.3,end=0.6)
+ pcols = colours[match(group,gu)]
+ nrows = nrow(cmat)
+ mtitle = paste(myTitle,'Heatmap: n contigs =',nrows)
+ if (nrows > nsamp) {
+ cmat = cmat[c(1:nsamp),]
+ mtitle = paste('Heatmap: Top ',nsamp,' DE contigs (of ',nrows,')',sep='')
+ }
+ newcolnames = substr(colnames(cmat),1,20)
+ colnames(cmat) = newcolnames
+ pdf(outpdfname)
+ heatmap(cmat,scale='row',main=mtitle,cexRow=0.3,cexCol=0.4,Rowv=NA,ColSideColors=pcols)
+ dev.off()
+}
+
+qqPlot = function(descr='qqplot',pvector, outpdf='qqplot.pdf',...)
+# stolen from https://gist.github.com/703512
+{
+ o = -log10(sort(pvector,decreasing=F))
+ e = -log10( 1:length(o)/length(o) )
+ o[o==-Inf] = reallysmall
+ o[o==Inf] = reallybig
+ maint = descr
+ pdf(outpdf)
+ plot(e,o,pch=19,cex=1, main=maint, ...,
+ xlab=expression(Expected~~-log[10](italic(p))),
+ ylab=expression(Observed~~-log[10](italic(p))),
+ xlim=c(0,max(e)), ylim=c(0,max(o)))
+ lines(e,e,col="red")
+ grid(col = "lightgray", lty = "dotted")
+ dev.off()
+}
+
+smearPlot = function(DGEList,deTags, outSmear, outMain)
+ {
+ pdf(outSmear)
+ plotSmear(DGEList,de.tags=deTags,main=outMain)
+ grid(col="lightgray", lty="dotted")
+ dev.off()
+ }
+
+boxPlot = function(rawrs,cleanrs,maint,myTitle,pdfname)
+{ #
+ nc = ncol(rawrs)
+ for (i in c(1:nc)) {rawrs[(rawrs[,i] < 0),i] = NA}
+ fullnames = colnames(rawrs)
+ newcolnames = substr(colnames(rawrs),1,20)
+ colnames(rawrs) = newcolnames
+ newcolnames = substr(colnames(cleanrs),1,20)
+ colnames(cleanrs) = newcolnames
+ defpar = par(no.readonly=T)
+ print.noquote('raw contig counts by sample:')
+ print.noquote(summary(rawrs))
+ print.noquote('normalised contig counts by sample:')
+ print.noquote(summary(cleanrs))
+ pdf(pdfname)
+ par(mfrow=c(1,2))
+ boxplot(rawrs,varwidth=T,notch=T,ylab='log contig count',col="maroon",las=3,cex.axis=0.35,main=paste('Raw:',maint))
+ grid(col="lightgray",lty="dotted")
+ boxplot(cleanrs,varwidth=T,notch=T,ylab='log contig count',col="maroon",las=3,cex.axis=0.35,main=paste('After ',maint))
+ grid(col="lightgray",lty="dotted")
+ dev.off()
+ pdfname = "sample_counts_histogram.pdf"
+ nc = ncol(rawrs)
+ print.noquote(paste('Using ncol rawrs=',nc))
+ ncroot = round(sqrt(nc))
+ if (ncroot*ncroot < nc) { ncroot = ncroot + 1 }
+ m = c()
+ for (i in c(1:nc)) {
+ rhist = hist(rawrs[,i],breaks=100,plot=F)
+ m = append(m,max(rhist\$counts))
+ }
+ ymax = max(m)
+ ncols = length(fullnames)
+ if (ncols > 20)
+ {
+ scale = 7*ncols/20
+ pdf(pdfname,width=scale,height=scale)
+ } else {
+ pdf(pdfname)
+ }
+ par(mfrow=c(ncroot,ncroot))
+ for (i in c(1:nc)) {
+ hist(rawrs[,i], main=paste("Contig logcount",i), xlab='log raw count', col="maroon",
+ breaks=100,sub=fullnames[i],cex=0.8,ylim=c(0,ymax))
+ }
+ dev.off()
+ par(defpar)
+
+}
+
+cumPlot = function(rawrs,cleanrs,maint,myTitle)
+{ # updated to use ecdf
+ pdfname = "Filtering_rowsum_bar_charts.pdf"
+ defpar = par(no.readonly=T)
+ lrs = log(rawrs,10)
+ lim = max(lrs)
+ pdf(pdfname)
+ par(mfrow=c(2,1))
+ hist(lrs,breaks=100,main=paste('Before:',maint),xlab="# Reads (log)",
+ ylab="Count",col="maroon",sub=myTitle, xlim=c(0,lim),las=1)
+ grid(col="lightgray", lty="dotted")
+ lrs = log(cleanrs,10)
+ hist(lrs,breaks=100,main=paste('After:',maint),xlab="# Reads (log)",
+ ylab="Count",col="maroon",sub=myTitle,xlim=c(0,lim),las=1)
+ grid(col="lightgray", lty="dotted")
+ dev.off()
+ par(defpar)
+}
+
+cumPlot1 = function(rawrs,cleanrs,maint,myTitle)
+{ # updated to use ecdf
+ pdfname = paste(gsub(" ","", myTitle , fixed=TRUE),"RowsumCum.pdf",sep='_')
+ pdf(pdfname)
+ par(mfrow=c(2,1))
+ lastx = max(rawrs)
+ rawe = knots(ecdf(rawrs))
+ cleane = knots(ecdf(cleanrs))
+ cy = 1:length(cleane)/length(cleane)
+ ry = 1:length(rawe)/length(rawe)
+ plot(rawe,ry,type='l',main=paste('Before',maint),xlab="Log Contig Total Reads",
+ ylab="Cumulative proportion",col="maroon",log='x',xlim=c(1,lastx),sub=myTitle)
+ grid(col="blue")
+ plot(cleane,cy,type='l',main=paste('After',maint),xlab="Log Contig Total Reads",
+ ylab="Cumulative proportion",col="maroon",log='x',xlim=c(1,lastx),sub=myTitle)
+ grid(col="blue")
+ dev.off()
+}
+
+
+
+doGSEAold = function(y=NULL,design=NULL,histgmt="",
+ bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
+ ntest=0, myTitle="myTitle", outfname="GSEA.xls", minnin=5, maxnin=2000,fdrthresh=0.05,fdrtype="BH")
+{
+ sink('Camera.log')
+ genesets = c()
+ if (bigmt > "")
+ {
+ bigenesets = readLines(bigmt)
+ genesets = bigenesets
+ }
+ if (histgmt > "")
+ {
+ hgenesets = readLines(histgmt)
+ if (bigmt > "") {
+ genesets = rbind(genesets,hgenesets)
+ } else {
+ genesets = hgenesets
+ } # use only history if no bi
+ }
+ print.noquote(paste("@@@read",length(genesets), 'genesets from',histgmt,bigmt))
+ genesets = strsplit(genesets,'\t') # tabular. genesetid\tURLorwhatever\tgene_1\t..\tgene_n
+ outf = outfname
+ head=paste(myTitle,'edgeR GSEA')
+ write(head,file=outfname,append=F)
+ ntest=length(genesets)
+ urownames = toupper(rownames(y))
+ upcam = c()
+ downcam = c()
+ for (i in 1:ntest) {
+ gs = unlist(genesets[i])
+ g = gs[1] # geneset_id
+ u = gs[2]
+ if (u > "") { u = paste("",u," ",sep="") }
+ glist = gs[3:length(gs)] # member gene symbols
+ glist = toupper(glist)
+ inglist = urownames %in% glist
+ nin = sum(inglist)
+ if ((nin > minnin) && (nin < maxnin)) {
+ ### print(paste('@@found',sum(inglist),'genes in glist'))
+ camres = camera(y=y,index=inglist,design=design)
+ if (! is.null(camres)) {
+ rownames(camres) = g # gene set name
+ camres = cbind(GeneSet=g,URL=u,camres)
+ if (camres\$Direction == "Up")
+ {
+ upcam = rbind(upcam,camres) } else {
+ downcam = rbind(downcam,camres)
+ }
+ }
+ }
+ }
+ uscam = upcam[order(upcam\$PValue),]
+ unadjp = uscam\$PValue
+ uscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ nup = max(10,sum((uscam\$adjPValue < fdrthresh)))
+ dscam = downcam[order(downcam\$PValue),]
+ unadjp = dscam\$PValue
+ dscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ ndown = max(10,sum((dscam\$adjPValue < fdrthresh)))
+ write.table(uscam,file=paste('camera_up',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ write.table(dscam,file=paste('camera_down',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera up top',nup,'gene sets:'))
+ write.table(head(uscam,nup),file="",quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera down top',ndown,'gene sets:'))
+ write.table(head(dscam,ndown),file="",quote=F,sep='\t',row.names=F)
+ sink()
+}
+
+
+
+
+doGSEA = function(y=NULL,design=NULL,histgmt="",
+ bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
+ ntest=0, myTitle="myTitle", outfname="GSEA.xls", minnin=5, maxnin=2000,fdrthresh=0.05,fdrtype="BH")
+{
+ sink('Camera.log')
+ genesets = c()
+ if (bigmt > "")
+ {
+ bigenesets = readLines(bigmt)
+ genesets = bigenesets
+ }
+ if (histgmt > "")
+ {
+ hgenesets = readLines(histgmt)
+ if (bigmt > "") {
+ genesets = rbind(genesets,hgenesets)
+ } else {
+ genesets = hgenesets
+ } # use only history if no bi
+ }
+ print.noquote(paste("@@@read",length(genesets), 'genesets from',histgmt,bigmt))
+ genesets = strsplit(genesets,'\t') # tabular. genesetid\tURLorwhatever\tgene_1\t..\tgene_n
+ outf = outfname
+ head=paste(myTitle,'edgeR GSEA')
+ write(head,file=outfname,append=F)
+ ntest=length(genesets)
+ urownames = toupper(rownames(y))
+ upcam = c()
+ downcam = c()
+ incam = c()
+ urls = c()
+ gsids = c()
+ for (i in 1:ntest) {
+ gs = unlist(genesets[i])
+ gsid = gs[1] # geneset_id
+ url = gs[2]
+ if (url > "") { url = paste("",url," ",sep="") }
+ glist = gs[3:length(gs)] # member gene symbols
+ glist = toupper(glist)
+ inglist = urownames %in% glist
+ nin = sum(inglist)
+ if ((nin > minnin) && (nin < maxnin)) {
+ incam = c(incam,inglist)
+ gsids = c(gsids,gsid)
+ urls = c(urls,url)
+ }
+ }
+ incam = as.list(incam)
+ names(incam) = gsids
+ allcam = camera(y=y,index=incam,design=design)
+ allcamres = cbind(geneset=gsids,allcam,URL=urls)
+ for (i in 1:ntest) {
+ camres = allcamres[i]
+ res = try(test = (camres\$Direction == "Up"))
+ if ("try-error" %in% class(res)) {
+ cat("test failed, camres = :")
+ print.noquote(camres)
+ } else { if (camres\$Direction == "Up")
+ { upcam = rbind(upcam,camres)
+ } else { downcam = rbind(downcam,camres)
+ }
+
+ }
+ }
+ uscam = upcam[order(upcam\$PValue),]
+ unadjp = uscam\$PValue
+ uscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ nup = max(10,sum((uscam\$adjPValue < fdrthresh)))
+ dscam = downcam[order(downcam\$PValue),]
+ unadjp = dscam\$PValue
+ dscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
+ ndown = max(10,sum((dscam\$adjPValue < fdrthresh)))
+ write.table(uscam,file=paste('camera_up',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ write.table(dscam,file=paste('camera_down',outfname,sep='_'),quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera up top',nup,'gene sets:'))
+ write.table(head(uscam,nup),file="",quote=F,sep='\t',row.names=F)
+ print.noquote(paste('@@@@@ Camera down top',ndown,'gene sets:'))
+ write.table(head(dscam,ndown),file="",quote=F,sep='\t',row.names=F)
+ sink()
+ }
+
+
+edgeIt = function (Count_Matrix=c(),group=c(),out_edgeR=F,out_VOOM=F,out_DESeq2=F,fdrtype='fdr',priordf=5,
+ fdrthresh=0.05,outputdir='.', myTitle='Differential Counts',libSize=c(),useNDF=F,
+ filterquantile=0.2, subjects=c(),mydesign=NULL,
+ doDESeq2=T,doVoom=T,doCamera=T,doedgeR=T,org='hg19',
+ histgmt="", bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
+ doCook=F,DESeq_fitType="parameteric")
+{
+ # Error handling
+ if (length(unique(group))!=2){
+ print("Number of conditions identified in experiment does not equal 2")
+ q()
+ }
+ require(edgeR)
+ options(width = 512)
+ mt = paste(unlist(strsplit(myTitle,'_')),collapse=" ")
+ allN = nrow(Count_Matrix)
+ nscut = round(ncol(Count_Matrix)/2)
+ colTotmillionreads = colSums(Count_Matrix)/1e6
+ counts.dataframe = as.data.frame(c())
+ rawrs = rowSums(Count_Matrix)
+ nonzerod = Count_Matrix[(rawrs > 0),] # remove all zero count genes
+ nzN = nrow(nonzerod)
+ nzrs = rowSums(nonzerod)
+ zN = allN - nzN
+ print('# Quantiles for non-zero row counts:',quote=F)
+ print(quantile(nzrs,probs=seq(0,1,0.1)),quote=F)
+ if (useNDF == T)
+ {
+ gt1rpin3 = rowSums(Count_Matrix/expandAsMatrix(colTotmillionreads,dim(Count_Matrix)) >= 1) >= nscut
+ lo = colSums(Count_Matrix[!gt1rpin3,])
+ workCM = Count_Matrix[gt1rpin3,]
+ cleanrs = rowSums(workCM)
+ cleanN = length(cleanrs)
+ meth = paste( "After removing",length(lo),"contigs with fewer than ",nscut," sample read counts >= 1 per million, there are",sep="")
+ print(paste("Read",allN,"contigs. Removed",zN,"contigs with no reads.",meth,cleanN,"contigs"),quote=F)
+ maint = paste('Filter >=1/million reads in >=',nscut,'samples')
+ } else {
+ useme = (nzrs > quantile(nzrs,filterquantile))
+ workCM = nonzerod[useme,]
+ lo = colSums(nonzerod[!useme,])
+ cleanrs = rowSums(workCM)
+ cleanN = length(cleanrs)
+ meth = paste("After filtering at count quantile =",filterquantile,", there are",sep="")
+ print(paste('Read',allN,"contigs. Removed",zN,"with no reads.",meth,cleanN,"contigs"),quote=F)
+ maint = paste('Filter below',filterquantile,'quantile')
+ }
+ cumPlot(rawrs=rawrs,cleanrs=cleanrs,maint=maint,myTitle=myTitle)
+ allgenes = rownames(workCM)
+ reg = "^chr([0-9]+):([0-9]+)-([0-9]+)"
+ genecards=" 0.8) # is ucsc style string
+ {
+ print("@@ using ucsc substitution for urls")
+ contigurls = paste0(ucsc,"&position=chr",testreg[,2],":",testreg[,3],"-",testreg[,4],"\'>",allgenes," ")
+ } else {
+ print("@@ using genecards substitution for urls")
+ contigurls = paste0(genecards,allgenes,"\'>",allgenes,"")
+ }
+ print.noquote("# urls")
+ print.noquote(head(contigurls))
+ print(paste("# Total low count contigs per sample = ",paste(lo,collapse=',')),quote=F)
+ cmrowsums = rowSums(workCM)
+ TName=unique(group)[1]
+ CName=unique(group)[2]
+ if (is.null(mydesign)) {
+ if (length(subjects) == 0)
+ {
+ mydesign = model.matrix(~group)
+ }
+ else {
+ subjf = factor(subjects)
+ mydesign = model.matrix(~subjf+group) # we block on subject so make group last to simplify finding it
+ }
+ }
+ print.noquote(paste('Using samples:',paste(colnames(workCM),collapse=',')))
+ print.noquote('Using design matrix:')
+ print.noquote(mydesign)
+ if (doedgeR) {
+ sink('edgeR.log')
+ #### Setup DGEList object
+ DGEList = DGEList(counts=workCM, group = group)
+ DGEList = calcNormFactors(DGEList)
+
+ DGEList = estimateGLMCommonDisp(DGEList,mydesign)
+ comdisp = DGEList\$common.dispersion
+ DGEList = estimateGLMTrendedDisp(DGEList,mydesign)
+ if (edgeR_priordf > 0) {
+ print.noquote(paste("prior.df =",edgeR_priordf))
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign,prior.df = edgeR_priordf)
+ } else {
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
+ }
+ DGLM = glmFit(DGEList,design=mydesign)
+ DE = glmLRT(DGLM,coef=ncol(DGLM\$design)) # always last one - subject is first if needed
+ efflib = DGEList\$samples\$lib.size*DGEList\$samples\$norm.factors
+ normData = (1e+06*DGEList\$counts/efflib)
+ uoutput = cbind(
+ Name=as.character(rownames(DGEList\$counts)),
+ DE\$table,
+ adj.p.value=p.adjust(DE\$table\$PValue, method=fdrtype),
+ Dispersion=DGEList\$tagwise.dispersion,totreads=cmrowsums,normData,
+ DGEList\$counts
+ )
+ soutput = uoutput[order(DE\$table\$PValue),] # sorted into p value order - for quick toptable
+ goodness = gof(DGLM, pcutoff=fdrthresh)
+ if (sum(goodness\$outlier) > 0) {
+ print.noquote('GLM outliers:')
+ print(paste(rownames(DGLM)[(goodness\$outlier)],collapse=','),quote=F)
+ } else {
+ print('No GLM fit outlier genes found\n')
+ }
+ z = limma::zscoreGamma(goodness\$gof.statistic, shape=goodness\$df/2, scale=2)
+ pdf("edgeR_GoodnessofFit.pdf")
+ qq = qqnorm(z, panel.first=grid(), main="tagwise dispersion")
+ abline(0,1,lwd=3)
+ points(qq\$x[goodness\$outlier],qq\$y[goodness\$outlier], pch=16, col="maroon")
+ dev.off()
+ estpriorn = getPriorN(DGEList)
+ print(paste("Common Dispersion =",comdisp,"CV = ",sqrt(comdisp),"getPriorN = ",estpriorn),quote=F)
+ efflib = DGEList\$samples\$lib.size*DGEList\$samples\$norm.factors
+ normData = (1e+06*DGEList\$counts/efflib)
+ uniqueg = unique(group)
+ #### Plot MDS
+ sample_colors = match(group,levels(group))
+ sampleTypes = levels(factor(group))
+ print.noquote(sampleTypes)
+ pdf("edgeR_MDSplot.pdf")
+ plotMDS.DGEList(DGEList,main=paste("edgeR MDS for",myTitle),cex=0.5,col=sample_colors,pch=sample_colors)
+ legend(x="topleft", legend = sampleTypes,col=c(1:length(sampleTypes)), pch=19)
+ grid(col="blue")
+ dev.off()
+ colnames(normData) = paste( colnames(normData),'N',sep="_")
+ print(paste('Raw sample read totals',paste(colSums(nonzerod,na.rm=T),collapse=',')))
+ nzd = data.frame(log(nonzerod + 1e-2,10))
+ try( boxPlot(rawrs=nzd,cleanrs=log(normData,10),maint='TMM Normalisation',myTitle=myTitle,pdfname="edgeR_raw_norm_counts_box.pdf") )
+ write.table(soutput,file=out_edgeR, quote=FALSE, sep="\t",row.names=F)
+ tt = cbind(
+ Name=as.character(rownames(DGEList\$counts)),
+ DE\$table,
+ adj.p.value=p.adjust(DE\$table\$PValue, method=fdrtype),
+ Dispersion=DGEList\$tagwise.dispersion,totreads=cmrowsums
+ )
+ print.noquote("# edgeR Top tags\n")
+ tt = cbind(tt,URL=contigurls) # add to end so table isn't laid out strangely
+ tt = tt[order(DE\$table\$PValue),]
+ print.noquote(tt[1:50,])
+ deTags = rownames(uoutput[uoutput\$adj.p.value < fdrthresh,])
+ nsig = length(deTags)
+ print(paste('#',nsig,'tags significant at adj p=',fdrthresh),quote=F)
+ deColours = ifelse(deTags,'red','black')
+ pdf("edgeR_BCV_vs_abundance.pdf")
+ plotBCV(DGEList, cex=0.3, main="Biological CV vs abundance")
+ dev.off()
+ dg = DGEList[order(DE\$table\$PValue),]
+ #normData = (1e+06 * dg\$counts/expandAsMatrix(dg\$samples\$lib.size, dim(dg)))
+ efflib = dg\$samples\$lib.size*dg\$samples\$norm.factors
+ normData = (1e+06*dg\$counts/efflib)
+ outpdfname="edgeR_top_100_heatmap.pdf"
+ hmap2(normData,nsamp=100,TName=TName,group=group,outpdfname=outpdfname,myTitle=paste('edgeR Heatmap',myTitle))
+ outSmear = "edgeR_smearplot.pdf"
+ outMain = paste("Smear Plot for ",TName,' Vs ',CName,' (FDR@',fdrthresh,' N = ',nsig,')',sep='')
+ smearPlot(DGEList=DGEList,deTags=deTags, outSmear=outSmear, outMain = outMain)
+ qqPlot(descr=paste(myTitle,'edgeR adj p QQ plot'),pvector=tt\$adj.p.value,outpdf='edgeR_qqplot.pdf')
+ norm.factor = DGEList\$samples\$norm.factors
+ topresults.edgeR = soutput[which(soutput\$adj.p.value < fdrthresh), ]
+ edgeRcountsindex = which(allgenes %in% rownames(topresults.edgeR))
+ edgeRcounts = rep(0, length(allgenes))
+ edgeRcounts[edgeRcountsindex] = 1 # Create venn diagram of hits
+ sink()
+ } ### doedgeR
+ if (doDESeq2 == T)
+ {
+ sink("DESeq2.log")
+ # DESeq2
+ require('DESeq2')
+ library('RColorBrewer')
+ if (length(subjects) == 0)
+ {
+ pdata = data.frame(Name=colnames(workCM),Rx=group,row.names=colnames(workCM))
+ deSEQds = DESeqDataSetFromMatrix(countData = workCM, colData = pdata, design = formula(~ Rx))
+ } else {
+ pdata = data.frame(Name=colnames(workCM),Rx=group,subjects=subjects,row.names=colnames(workCM))
+ deSEQds = DESeqDataSetFromMatrix(countData = workCM, colData = pdata, design = formula(~ subjects + Rx))
+ }
+ #DESeq2 = DESeq(deSEQds,fitType='local',pAdjustMethod=fdrtype)
+ #rDESeq = results(DESeq2)
+ #newCountDataSet(workCM, group)
+ deSeqDatsizefac = estimateSizeFactors(deSEQds)
+ deSeqDatdisp = estimateDispersions(deSeqDatsizefac,fitType=DESeq_fitType)
+ resDESeq = nbinomWaldTest(deSeqDatdisp, pAdjustMethod=fdrtype)
+ rDESeq = as.data.frame(results(resDESeq))
+ rDESeq = cbind(Contig=rownames(workCM),rDESeq,NReads=cmrowsums,URL=contigurls)
+ srDESeq = rDESeq[order(rDESeq\$pvalue),]
+ qqPlot(descr=paste(myTitle,'DESeq2 adj p qq plot'),pvector=rDESeq\$padj,outpdf='DESeq2_qqplot.pdf')
+ cat("# DESeq top 50\n")
+ print.noquote(srDESeq[1:50,])
+ write.table(srDESeq,file=out_DESeq2, quote=FALSE, sep="\t",row.names=F)
+ topresults.DESeq = rDESeq[which(rDESeq\$padj < fdrthresh), ]
+ DESeqcountsindex = which(allgenes %in% rownames(topresults.DESeq))
+ DESeqcounts = rep(0, length(allgenes))
+ DESeqcounts[DESeqcountsindex] = 1
+ pdf("DESeq2_dispersion_estimates.pdf")
+ plotDispEsts(resDESeq)
+ dev.off()
+ ysmall = abs(min(rDESeq\$log2FoldChange))
+ ybig = abs(max(rDESeq\$log2FoldChange))
+ ylimit = min(4,ysmall,ybig)
+ pdf("DESeq2_MA_plot.pdf")
+ plotMA(resDESeq,main=paste(myTitle,"DESeq2 MA plot"),ylim=c(-ylimit,ylimit))
+ dev.off()
+ rlogres = rlogTransformation(resDESeq)
+ sampledists = dist( t( assay(rlogres) ) )
+ sdmat = as.matrix(sampledists)
+ pdf("DESeq2_sample_distance_plot.pdf")
+ heatmap.2(sdmat,trace="none",main=paste(myTitle,"DESeq2 sample distances"),
+ col = colorRampPalette( rev(brewer.pal(9, "RdBu")) )(255))
+ dev.off()
+ ###outpdfname="DESeq2_top50_heatmap.pdf"
+ ###hmap2(sresDESeq,nsamp=50,TName=TName,group=group,outpdfname=outpdfname,myTitle=paste('DESeq2 vst rlog Heatmap',myTitle))
+ sink()
+ result = try( (ppca = plotPCA( varianceStabilizingTransformation(deSeqDatdisp,blind=T), intgroup=c("Rx","Name")) ) )
+ if ("try-error" %in% class(result)) {
+ print.noquote('DESeq2 plotPCA failed.')
+ } else {
+ pdf("DESeq2_PCA_plot.pdf")
+ #### wtf - print? Seems needed to get this to work
+ print(ppca)
+ dev.off()
+ }
+ }
+
+ if (doVoom == T) {
+ sink('VOOM.log')
+ if (doedgeR == F) {
+ #### Setup DGEList object
+ DGEList = DGEList(counts=workCM, group = group)
+ DGEList = calcNormFactors(DGEList)
+ DGEList = estimateGLMCommonDisp(DGEList,mydesign)
+ DGEList = estimateGLMTrendedDisp(DGEList,mydesign)
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
+ DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
+ norm.factor = DGEList\$samples\$norm.factors
+ }
+ pdf("VOOM_mean_variance_plot.pdf")
+ dat.voomed = voom(DGEList, mydesign, plot = TRUE, lib.size = colSums(workCM) * norm.factor)
+ dev.off()
+ # Use limma to fit data
+ fit = lmFit(dat.voomed, mydesign)
+ fit = eBayes(fit)
+ rvoom = topTable(fit, coef = length(colnames(mydesign)), adj = fdrtype, n = Inf, sort="none")
+ qqPlot(descr=paste(myTitle,'VOOM-limma adj p QQ plot'),pvector=rvoom\$adj.P.Val,outpdf='VOOM_qqplot.pdf')
+ rownames(rvoom) = rownames(workCM)
+ rvoom = cbind(rvoom,NReads=cmrowsums,URL=contigurls)
+ srvoom = rvoom[order(rvoom\$P.Value),]
+ cat("# VOOM top 50\n")
+ print(srvoom[1:50,])
+ write.table(srvoom,file=out_VOOM, quote=FALSE, sep="\t",row.names=F)
+ # Use an FDR cutoff to find interesting samples for edgeR, DESeq and voom/limma
+ topresults.voom = rvoom[which(rvoom\$adj.P.Val < fdrthresh), ]
+ voomcountsindex = which(allgenes %in% topresults.voom\$ID)
+ voomcounts = rep(0, length(allgenes))
+ voomcounts[voomcountsindex] = 1
+ sink()
+ }
+
+ if (doCamera) {
+ doGSEA(y=DGEList,design=mydesign,histgmt=histgmt,bigmt=bigmt,ntest=20,myTitle=myTitle,
+ outfname=paste(mt,"GSEA.xls",sep="_"),fdrthresh=fdrthresh,fdrtype=fdrtype)
+ }
+
+ if ((doDESeq2==T) || (doVoom==T) || (doedgeR==T)) {
+ if ((doVoom==T) && (doDESeq2==T) && (doedgeR==T)) {
+ vennmain = paste(mt,'Voom,edgeR and DESeq2 overlap at FDR=',fdrthresh)
+ counts.dataframe = data.frame(edgeR = edgeRcounts, DESeq2 = DESeqcounts,
+ VOOM_limma = voomcounts, row.names = allgenes)
+ } else if ((doDESeq2==T) && (doedgeR==T)) {
+ vennmain = paste(mt,'DESeq2 and edgeR overlap at FDR=',fdrthresh)
+ counts.dataframe = data.frame(edgeR = edgeRcounts, DESeq2 = DESeqcounts, row.names = allgenes)
+ } else if ((doVoom==T) && (doedgeR==T)) {
+ vennmain = paste(mt,'Voom and edgeR overlap at FDR=',fdrthresh)
+ counts.dataframe = data.frame(edgeR = edgeRcounts, VOOM_limma = voomcounts, row.names = allgenes)
+ }
+
+ if (nrow(counts.dataframe > 1)) {
+ counts.venn = vennCounts(counts.dataframe)
+ vennf = "Venn_significant_genes_overlap.pdf"
+ pdf(vennf)
+ vennDiagram(counts.venn,main=vennmain,col="maroon")
+ dev.off()
+ }
+ } #### doDESeq2 or doVoom
+
+}
+#### Done
+
+###sink(stdout(),append=T,type="message")
+builtin_gmt = ""
+history_gmt = ""
+history_gmt_name = ""
+out_edgeR = F
+out_DESeq2 = F
+out_VOOM = "$out_VOOM"
+doDESeq2 = $DESeq2.doDESeq2 # make these T or F
+doVoom = $doVoom
+doCamera = F
+doedgeR = $edgeR.doedgeR
+edgeR_priordf = 0
+
+
+#if $doVoom == "T":
+ out_VOOM = "$out_VOOM"
+#end if
+
+#if $DESeq2.doDESeq2 == "T":
+ out_DESeq2 = "$out_DESeq2"
+ DESeq_fitType = "$DESeq2.DESeq_fitType"
+#end if
+
+#if $edgeR.doedgeR == "T":
+ out_edgeR = "$out_edgeR"
+ edgeR_priordf = $edgeR.edgeR_priordf
+#end if
+
+
+if (sum(c(doedgeR,doVoom,doDESeq2)) == 0)
+{
+write("No methods chosen - nothing to do! Please try again after choosing one or more methods", stderr())
+quit(save="no",status=2)
+}
+
+Out_Dir = "$html_file.files_path"
+Input = "$input1"
+TreatmentName = "$treatment_name"
+TreatmentCols = "$Treat_cols"
+ControlName = "$control_name"
+ControlCols= "$Control_cols"
+org = "$input1.dbkey"
+if (org == "") { org = "hg19"}
+fdrtype = "$fdrtype"
+fdrthresh = $fdrthresh
+useNDF = $useNDF
+fQ = $fQ # non-differential centile cutoff
+myTitle = "$title"
+sids = strsplit("$subjectids",',')
+subjects = unlist(sids)
+nsubj = length(subjects)
+TCols = as.numeric(strsplit(TreatmentCols,",")[[1]])-1
+CCols = as.numeric(strsplit(ControlCols,",")[[1]])-1
+cat('Got TCols=')
+cat(TCols)
+cat('; CCols=')
+cat(CCols)
+cat('\n')
+useCols = c(TCols,CCols)
+if (file.exists(Out_Dir) == F) dir.create(Out_Dir)
+Count_Matrix = read.table(Input,header=T,row.names=1,sep='\t') #Load tab file assume header
+snames = colnames(Count_Matrix)
+nsamples = length(snames)
+if (nsubj > 0 & nsubj != nsamples) {
+options("show.error.messages"=T)
+mess = paste('Fatal error: Supplied subject id list',paste(subjects,collapse=','),
+ 'has length',nsubj,'but there are',nsamples,'samples',paste(snames,collapse=','))
+write(mess, stderr())
+quit(save="no",status=4)
+}
+if (length(subjects) != 0) {subjects = subjects[useCols]}
+Count_Matrix = Count_Matrix[,useCols] ### reorder columns
+rn = rownames(Count_Matrix)
+islib = rn %in% c('librarySize','NotInBedRegions')
+LibSizes = Count_Matrix[subset(rn,islib),][1] # take first
+Count_Matrix = Count_Matrix[subset(rn,! islib),]
+group = c(rep(TreatmentName,length(TCols)), rep(ControlName,length(CCols)) ) #Build a group descriptor
+group = factor(group, levels=c(ControlName,TreatmentName))
+colnames(Count_Matrix) = paste(group,colnames(Count_Matrix),sep="_") #Relable columns
+results = edgeIt(Count_Matrix=Count_Matrix,group=group, out_edgeR=out_edgeR, out_VOOM=out_VOOM, out_DESeq2=out_DESeq2,
+ fdrtype='BH',mydesign=NULL,priordf=edgeR_priordf,fdrthresh=fdrthresh,outputdir='.',
+ myTitle=myTitle,useNDF=F,libSize=c(),filterquantile=fQ,subjects=subjects,
+ doDESeq2=doDESeq2,doVoom=doVoom,doCamera=doCamera,doedgeR=doedgeR,org=org,
+ histgmt=history_gmt,bigmt=builtin_gmt,DESeq_fitType=DESeq_fitType)
+sessionInfo()
+]]>
+
+
+
+
+**What it does**
+
+Allows short read sequence counts from controlled experiments to be analysed for differentially expressed genes.
+Optionally adds a term for subject if not all samples are independent or if some other factor needs to be blocked in the design.
+
+**Input**
+
+Requires a count matrix as a tabular file. These are best made using the companion HTSeq_ based counter Galaxy wrapper
+and your fave gene model to generate inputs. Each row is a genomic feature (gene or exon eg) and each column the
+non-negative integer count of reads from one sample overlapping the feature.
+The matrix must have a header row uniquely identifying the source samples, and unique row names in
+the first column. Typically the row names are gene symbols or probe ids for downstream use in GSEA and other methods.
+
+**Specifying comparisons**
+
+This is basically dumbed down for two factors - case vs control.
+
+More complex interfaces are possible but painful at present.
+Probably need to specify a phenotype file to do this better.
+Work in progress. Send code.
+
+If you have (eg) paired samples and wish to include a term in the GLM to account for some other factor (subject in the case of paired samples),
+put a comma separated list of indicators for every sample (whether modelled or not!) indicating (eg) the subject number or
+A list of integers, one for each subject or an empty string if samples are all independent.
+If not empty, there must be exactly as many integers in the supplied integer list as there are columns (samples) in the count matrix.
+Integers for samples that are not in the analysis *must* be present in the string as filler even if not used.
+
+So if you have 2 pairs out of 6 samples, you need to put in unique integers for the unpaired ones
+eg if you had 6 samples with the first two independent but the second and third pairs each being from independent subjects. you might use
+8,9,1,1,2,2
+as subject IDs to indicate two paired samples from the same subject in columns 3/4 and 5/6
+
+**Methods available**
+
+You can run 3 popular Bioconductor packages available for count data.
+
+edgeR - see edgeR_ for details
+
+VOOM/limma - see limma_VOOM_ for details
+
+DESeq2 - see DESeq2_ for details
+
+and optionally camera in edgeR which works better if MSigDB is installed.
+
+**Outputs**
+
+Some helpful plots and analysis results. Note that most of these are produced using R code
+suggested by the excellent documentation and vignettes for the Bioconductor
+packages invoked. The Tool Factory is used to automatically lay these out for you to enjoy.
+
+**Note on Voom**
+
+The voom from limma version 3.16.6 help in R includes this from the authors - but you should read the paper to interpret this method.
+
+This function is intended to process RNA-Seq or ChIP-Seq data prior to linear modelling in limma.
+
+voom is an acronym for mean-variance modelling at the observational level.
+The key concern is to estimate the mean-variance relationship in the data, then use this to compute appropriate weights for each observation.
+Count data almost show non-trivial mean-variance relationships. Raw counts show increasing variance with increasing count size, while log-counts typically show a decreasing mean-variance trend.
+This function estimates the mean-variance trend for log-counts, then assigns a weight to each observation based on its predicted variance.
+The weights are then used in the linear modelling process to adjust for heteroscedasticity.
+
+In an experiment, a count value is observed for each tag in each sample. A tag-wise mean-variance trend is computed using lowess.
+The tag-wise mean is the mean log2 count with an offset of 0.5, across samples for a given tag.
+The tag-wise variance is the quarter-root-variance of normalized log2 counts per million values with an offset of 0.5, across samples for a given tag.
+Tags with zero counts across all samples are not included in the lowess fit. Optional normalization is performed using normalizeBetweenArrays.
+Using fitted values of log2 counts from a linear model fit by lmFit, variances from the mean-variance trend were interpolated for each observation.
+This was carried out by approxfun. Inverse variance weights can be used to correct for mean-variance trend in the count data.
+
+
+Author(s)
+
+Charity Law and Gordon Smyth
+
+References
+
+Law, CW (2013). Precision weights for gene expression analysis. PhD Thesis. University of Melbourne, Australia.
+
+Law, CW, Chen, Y, Shi, W, Smyth, GK (2013). Voom! Precision weights unlock linear model analysis tools for RNA-seq read counts.
+Technical Report 1 May 2013, Bioinformatics Division, Walter and Eliza Hall Institute of Medical Reseach, Melbourne, Australia.
+http://www.statsci.org/smyth/pubs/VoomPreprint.pdf
+
+See Also
+
+A voom case study is given in the edgeR User's Guide.
+
+vooma is a similar function but for microarrays instead of RNA-seq.
+
+
+***old rant on changes to Bioconductor package variable names between versions***
+
+The edgeR authors made a small cosmetic change in the name of one important variable (from p.value to PValue)
+breaking this and all other code that assumed the old name for this variable,
+between edgeR2.4.4 and 2.4.6 (the version for R 2.14 as at the time of writing).
+This means that all code using edgeR is sensitive to the version. I think this was a very unwise thing
+to do because it wasted hours of my time to track down and will similarly cost other edgeR users dearly
+when their old scripts break. This tool currently now works with 2.4.6.
+
+**Note on prior.N**
+
+http://seqanswers.com/forums/showthread.php?t=5591 says:
+
+*prior.n*
+
+The value for prior.n determines the amount of smoothing of tagwise dispersions towards the common dispersion.
+You can think of it as like a "weight" for the common value. (It is actually the weight for the common likelihood
+in the weighted likelihood equation). The larger the value for prior.n, the more smoothing, i.e. the closer your
+tagwise dispersion estimates will be to the common dispersion. If you use a prior.n of 1, then that gives the
+common likelihood the weight of one observation.
+
+In answer to your question, it is a good thing to squeeze the tagwise dispersions towards a common value,
+or else you will be using very unreliable estimates of the dispersion. I would not recommend using the value that
+you obtained from estimateSmoothing()---this is far too small and would result in virtually no moderation
+(squeezing) of the tagwise dispersions. How many samples do you have in your experiment?
+What is the experimental design? If you have few samples (less than 6) then I would suggest a prior.n of at least 10.
+If you have more samples, then the tagwise dispersion estimates will be more reliable,
+so you could consider using a smaller prior.n, although I would hesitate to use a prior.n less than 5.
+
+
+From Bioconductor Digest, Vol 118, Issue 5, Gordon writes:
+
+Dear Dorota,
+
+The important settings are prior.df and trend.
+
+prior.n and prior.df are related through prior.df = prior.n * residual.df,
+and your experiment has residual.df = 36 - 12 = 24. So the old setting of
+prior.n=10 is equivalent for your data to prior.df = 240, a very large
+value. Going the other way, the new setting of prior.df=10 is equivalent
+to prior.n=10/24.
+
+To recover old results with the current software you would use
+
+ estimateTagwiseDisp(object, prior.df=240, trend="none")
+
+To get the new default from old software you would use
+
+ estimateTagwiseDisp(object, prior.n=10/24, trend=TRUE)
+
+Actually the old trend method is equivalent to trend="loess" in the new
+software. You should use plotBCV(object) to see whether a trend is
+required.
+
+Note you could also use
+
+ prior.n = getPriorN(object, prior.df=10)
+
+to map between prior.df and prior.n.
+
+----
+
+**Attributions**
+
+edgeR - edgeR_
+
+VOOM/limma - limma_VOOM_
+
+DESeq2 - DESeq2_ for details
+
+See above for Bioconductor package documentation for packages exposed in Galaxy by this tool and app store package.
+
+Galaxy_ (that's what you are using right now!) for gluing everything together
+
+Otherwise, all code and documentation comprising this tool was written by Ross Lazarus and is
+licensed to you under the LGPL_ like other rgenetics artefacts
+
+.. _LGPL: http://www.gnu.org/copyleft/lesser.html
+.. _HTSeq: http://www-huber.embl.de/users/anders/HTSeq/doc/index.html
+.. _edgeR: http://www.bioconductor.org/packages/release/bioc/html/edgeR.html
+.. _DESeq2: http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html
+.. _limma_VOOM: http://www.bioconductor.org/packages/release/bioc/html/limma.html
+.. _Galaxy: http://getgalaxy.org
+
+
+
+
+
diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/test-data/edgeRtest1out.html
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/test-data/edgeRtest1out.html Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,733 @@
+
+
+
+
+
+
+
+
+
+
+
Galaxy Tool "DifferentialCounts" run at 07/08/2013 15:46:55
+
DESeq2 images and outputs
+(Click on a thumbnail image to download the corresponding original PDF image)
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
DESeq2 log output
+
+
+
+# DESeq top 50
+
+ Contig baseMean log2FoldChange lfcSE pvalue padj NReads URL
+
+Mir192 Mir192 271352.97636 6.965264 0.2150593 4.096936e-230 4.576278e-227 2325567 Mir192
+
+Mir122a Mir122a 10112.31117 10.312083 0.3292695 2.649323e-215 1.479647e-212 90428 Mir122a
+
+Mir149 Mir149 810.35429 -6.911118 0.2341392 1.735537e-191 6.461982e-189 6164 Mir149
+
+Mir23a Mir23a 1289.18043 -3.104086 0.1191688 1.424246e-149 3.977206e-147 10118 Mir23a
+
+Mir181d Mir181d 275.22797 -3.581172 0.1778187 3.329371e-90 7.437816e-88 2139 Mir181d
+
+Mir204 Mir204 347.57397 -7.284200 0.3771119 3.959336e-83 7.370965e-81 2601 Mir204
+
+Mir23b Mir23b 2028.55377 -2.065110 0.1085802 1.182361e-80 1.886711e-78 16387 Mir23b
+
+Mir27a Mir27a 2788.72629 -3.016676 0.1688167 2.036708e-71 2.843754e-69 21886 Mir27a
+
+Mir195 Mir195 519.86200 -3.152795 0.1784796 7.838123e-70 9.727982e-68 3962 Mir195
+
+Mir194-2 Mir194-2 391.65678 5.222911 0.3099275 1.013490e-63 1.132068e-61 3570 Mir194-2
+
+Mir208b Mir208b 1649.77924 -11.396172 0.6771238 1.464479e-63 1.487112e-61 14756 Mir208b
+
+Mir10b Mir10b 27820.40551 -5.071453 0.3044889 2.754493e-62 2.563974e-60 197340 Mir10b
+
+Mir181c Mir181c 2765.96510 -3.660964 0.2275711 3.141153e-58 2.698975e-56 23605 Mir181c
+
+Mir208a Mir208a 616.76981 -10.356524 0.6559217 3.688385e-56 2.942804e-54 4638 Mir208a
+
+Mir490 Mir490 220.99790 -8.059660 0.5142876 2.369067e-55 1.764165e-53 1741 Mir490
+
+Mir203 Mir203 772.92882 1.990849 0.1274099 4.877239e-55 3.404923e-53 6739 Mir203
+
+Mir215 Mir215 152.78082 -3.004380 0.1939090 3.822339e-54 2.511502e-52 1182 Mir215
+
+Dnm3os Dnm3os 179.61643 -3.278392 0.2166491 9.922020e-52 6.157165e-50 1401 Dnm3os
+
+Mir214 Mir214 134.69038 -3.216444 0.2154916 2.230148e-50 1.311093e-48 1048 Mir214
+
+Mir21 Mir21 26121.31011 2.963903 0.2008617 2.817434e-49 1.573537e-47 229120 Mir21
+
+Mir1948 Mir1948 263.89527 7.074045 0.4867225 7.374030e-48 3.922282e-46 2404 Mir1948
+
+Mir27b Mir27b 76478.05753 -1.904653 0.1312889 1.088626e-47 5.527251e-46 625308 Mir27b
+
+Rabggtb Rabggtb 2257.19195 1.988368 0.1401741 1.134862e-45 5.511484e-44 19535 Rabggtb
+
+Mir499 Mir499 712.45950 -10.577061 0.7528467 7.766408e-45 3.614616e-43 6527 Mir499
+
+Mir101b Mir101b 6846.19683 3.791681 0.2809666 1.670548e-41 7.464007e-40 59019 Mir101b
+
+Mir132 Mir132 106.46062 -2.797928 0.2083376 4.046163e-41 1.738294e-39 857 Mir132
+
+Mir143hg Mir143hg 180217.77425 -2.169143 0.1685614 6.764675e-38 2.798571e-36 1407364 Mir143hg
+
+Mir143 Mir143 179219.35960 -2.170303 0.1696199 1.746403e-37 6.966899e-36 1399819 Mir143
+
+Mir155 Mir155 57.66182 -3.788079 0.3056585 2.845488e-35 1.096004e-33 463 Mir155
+
+Mir322 Mir322 899.53469 -3.126011 0.2622595 9.363374e-33 3.486296e-31 7074 Mir322
+
+Mir378 Mir378 483.21548 -2.994300 0.2577321 3.343457e-31 1.204723e-29 4075 Mir378
+
+Mir24-2 Mir24-2 424.48288 -2.712674 0.2361028 1.491830e-30 5.049617e-29 3470 Mir24-2
+
+Mir3074-2 Mir3074-2 424.48288 -2.712674 0.2361028 1.491830e-30 5.049617e-29 3470 Mir3074-2
+
+Mir199b Mir199b 47.84725 -5.294373 0.4644474 4.215162e-30 1.384805e-28 370 Mir199b
+
+Mir802 Mir802 166.83414 8.816580 0.7782636 9.478527e-30 3.025004e-28 1514 Mir802
+
+Mir125b-2 Mir125b-2 493.08516 -2.919341 0.2631193 1.324797e-28 4.110551e-27 3837 Mir125b-2
+
+Mir301 Mir301 260.53406 -1.676984 0.1526772 4.570133e-28 1.379686e-26 2119 Mir301
+
+Snord104 Snord104 3851.90119 2.386573 0.2173857 4.847914e-28 1.425032e-26 33458 Snord104
+
+Mir150 Mir150 553.20599 -2.836881 0.2595088 8.127991e-28 2.327940e-26 4229 Mir150
+
+Mir148a Mir148a 118994.46955 2.678852 0.2481801 3.675045e-27 1.026256e-25 1002397 Mir148a
+
+5430416N02Rik 5430416N02Rik 62.15966 3.089960 0.2941123 8.101331e-26 2.207119e-24 564 5430416N02Rik
+
+Mir193 Mir193 45.70861 4.991530 0.4814098 3.446492e-25 9.166027e-24 421 Mir193
+
+Mir3073 Mir3073 98.93199 8.208709 0.7944742 5.036320e-25 1.308272e-23 904 Mir3073
+
+Mir125b-1 Mir125b-1 79.01988 -3.020660 0.2937360 8.355633e-25 2.121191e-23 609 Mir125b-1
+
+2610203C20Rik 2610203C20Rik 79.17666 -3.023491 0.2948614 1.136165e-24 2.820214e-23 610 2610203C20Rik
+
+Mir181a-1 Mir181a-1 59.53826 -3.151487 0.3211628 9.923707e-23 2.409735e-21 506 Mir181a-1
+
+Mir184 Mir184 32.23796 -4.865023 0.4962776 1.092606e-22 2.596683e-21 247 Mir184
+
+Mir199a-2 Mir199a-2 44.84878 -3.422216 0.3545647 4.826269e-22 1.123113e-20 352 Mir199a-2
+
+Snord91a Snord91a 168.95251 2.700421 0.2835464 1.670595e-21 3.808275e-20 1437 Snord91a
+
+Mir200b Mir200b 87.13638 5.940702 0.6338554 7.094881e-21 1.584996e-19 888 Mir200b
+
+
+
+
+
DifferentialCounts log output
+
+
+
+Loading required package: gtools
+
+Loading required package: gdata
+
+gdata: read.xls support for 'XLS' (Excel 97-2004) files ENABLED.
+
+gdata: read.xls support for 'XLSX' (Excel 2007+) files ENABLED.
+
+Attaching package: ‘gdata’
+
+The following object is masked from ‘package:stats’:
+
+ nobs
+
+The following object is masked from ‘package:utils’:
+
+ object.size
+
+Loading required package: caTools
+
+Loading required package: grid
+
+Loading required package: KernSmooth
+
+KernSmooth 2.23 loaded
+
+Copyright M. P. Wand 1997-2009
+
+Loading required package: MASS
+
+Attaching package: ‘gplots’
+
+The following object is masked from ‘package:stats’:
+
+ lowess
+
+Loading required package: methods
+
+Loading required package: limma
+
+Loading required package: splines
+
+Loading required package: DESeq2
+
+Loading required package: GenomicRanges
+
+Loading required package: BiocGenerics
+
+Loading required package: parallel
+
+Attaching package: ‘BiocGenerics’
+
+The following object is masked from ‘package:parallel’:
+
+ clusterApply, clusterApplyLB, clusterCall, clusterEvalQ, clusterExport, clusterMap, parApply, parCapply, parLapply, parLapplyLB, parRapply, parSapply, parSapplyLB
+
+The following object is masked from ‘package:gdata’:
+
+ combine
+
+The following object is masked from ‘package:stats’:
+
+ xtabs
+
+The following object is masked from ‘package:base’:
+
+ anyDuplicated, as.data.frame, cbind, colnames, duplicated, eval, Filter, Find, get, intersect, lapply, Map, mapply, match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, Position, rank, rbind, Reduce, rep.int, rownames, sapply, setdiff, sort, table, tapply, union, unique, unlist
+
+Loading required package: IRanges
+
+Attaching package: ‘IRanges’
+
+The following object is masked from ‘package:gplots’:
+
+ space
+
+The following object is masked from ‘package:caTools’:
+
+ runmean
+
+The following object is masked from ‘package:gdata’:
+
+ trim
+
+Loading required package: Biobase
+
+Welcome to Bioconductor
+
+ Vignettes contain introductory material; view with 'browseVignettes()'. To cite Bioconductor, see 'citation("Biobase")', and for packages 'citation("pkgname")'.
+
+Loading required package: lattice
+
+Loading required package: Rcpp
+
+Loading required package: RcppArmadillo
+
+Attaching package: ‘DESeq2’
+
+The following object is masked from ‘package:limma’:
+
+ plotMA
+
+gene-wise dispersion estimates
+
+mean-dispersion relationship
+
+final dispersion estimates
+
+you had estimated dispersions, replacing these
+
+gene-wise dispersion estimates
+
+mean-dispersion relationship
+
+final dispersion estimates
+
+you had estimated dispersions, replacing these
+
+gene-wise dispersion estimates
+
+mean-dispersion relationship
+
+final dispersion estimates
+
+Warning messages:
+
+1: In bplt(at[i], wid = width[i], stats = z$stats[, i], out = z$out[z$group == :
+
+ Outlier (-Inf) in boxplot 1 is not drawn
+
+2: In bplt(at[i], wid = width[i], stats = z$stats[, i], out = z$out[z$group == :
+
+ Outlier (-Inf) in boxplot 3 is not drawn
+
+3: In bxp(list(stats = c(-0.430723026286372, -0.127900608036896, 0.474159383291067, :
+
+ some notches went outside hinges ('box'): maybe set notch=FALSE
+
+4: In par(defpar) : calling par(new=TRUE) with no plot
+
+
+
+
+
VOOM images and outputs
+(Click on a thumbnail image to download the corresponding original PDF image)
+
+
+
+
+
+
+
+
+
+
VOOM log output
+
+
+
+# VOOM top 50
+
+ ID logFC AveExpr t P.Value adj.P.Val B NReads URL
+
+Mir192 Mir192 6.948883 14.6763803 42.722954 2.301199e-16 2.625668e-13 27.266471 2325567 Mir192
+
+Mir208a Mir208a -11.015018 3.9395538 -23.252407 1.118938e-12 6.383542e-10 17.208662 4638 Mir208a
+
+Mir122a Mir122a 10.426125 8.1698641 21.722912 2.859682e-12 1.087633e-09 17.760171 90428 Mir122a
+
+Mir149 Mir149 -7.030463 6.3160807 -20.883835 4.915491e-12 1.402144e-09 17.277609 6164 Mir149
+
+Mir208b Mir208b -12.433228 4.6076218 -19.592458 1.179199e-11 2.690931e-09 15.683666 14756 Mir208b
+
+Mir10b Mir10b -5.130915 12.2628672 -18.242023 3.124991e-11 4.963978e-09 16.221503 197340 Mir10b
+
+Mir143hg Mir143hg -2.249221 16.2444825 -18.082481 3.521739e-11 4.963978e-09 16.026695 1407364 Mir143hg
+
+Mir143 Mir143 -2.251067 16.2358599 -18.081481 3.524391e-11 4.963978e-09 16.026084 1399819 Mir143
+
+Mir499 Mir499 -11.567529 3.7874598 -17.942086 3.915496e-11 4.963978e-09 14.821741 6527 Mir499
+
+Mir802 Mir802 9.158434 2.9157675 17.316522 6.338616e-11 7.232360e-09 14.381577 1514 Mir802
+
+Mir3073 Mir3073 8.420542 2.5457189 16.702657 1.033066e-10 1.036045e-08 13.985845 904 Mir3073
+
+Mir148a Mir148a 2.638213 15.4435820 16.548188 1.171186e-10 1.036045e-08 14.814792 1002397 Mir148a
+
+Mir101b Mir101b 3.765722 10.8508440 16.538566 1.180419e-10 1.036045e-08 14.900027 59019 Mir101b
+
+Mir490 Mir490 -8.474378 3.7506957 -16.259650 1.484816e-10 1.210125e-08 13.424617 1741 Mir490
+
+Mir21 Mir21 2.938537 13.1642917 15.375404 3.148335e-10 2.394833e-08 13.867698 229120 Mir21
+
+Mir181c Mir181c -3.742560 9.6295577 -15.242361 3.537063e-10 2.522368e-08 13.810405 23605 Mir181c
+
+Mir204 Mir204 -7.684425 4.7751735 -15.033484 4.254268e-10 2.855364e-08 12.822427 2601 Mir204
+
+Mir23a Mir23a -3.165768 8.7896592 -14.631179 6.110682e-10 3.873493e-08 13.269174 10118 Mir23a
+
+Mir181d Mir181d -3.636211 6.3713218 -14.317073 8.157508e-10 4.898798e-08 12.956333 2139 Mir181d
+
+Mir133b Mir133b -6.493549 1.2544862 -13.969968 1.129934e-09 6.446275e-08 11.982684 159 Mir133b
+
+Mir27a Mir27a -3.106935 9.9255796 -13.838251 1.281011e-09 6.960160e-08 12.513086 21886 Mir27a
+
+Mir194-2 Mir194-2 5.264136 6.0897615 13.044012 2.792884e-09 1.448491e-07 11.715753 3570 Mir194-2
+
+Mir195 Mir195 -3.216595 7.4509350 -12.869478 3.332788e-09 1.653353e-07 11.587523 3962 Mir195
+
+Mir27b Mir27b -1.976376 15.0957731 -11.756036 1.082197e-08 5.144946e-07 10.127719 625308 Mir27b
+
+Mir378 Mir378 -3.097393 7.3832049 -11.684163 1.171371e-08 5.346138e-07 10.329692 4075 Mir378
+
+Snord104 Snord104 2.337374 10.6109024 11.495675 1.444482e-08 6.339052e-07 10.023395 33458 Snord104
+
+Mir1983 Mir1983 -5.895500 0.9931851 -11.445812 1.527548e-08 6.441605e-07 9.749260 101 Mir1983
+
+Mir322 Mir322 -3.296618 8.2153415 -11.415362 1.580762e-08 6.441605e-07 10.008472 7074 Mir322
+
+Mir200a Mir200a 6.191561 1.7981309 11.322172 1.756229e-08 6.909853e-07 9.662295 264 Mir200a
+
+Mir215 Mir215 -3.045873 5.7544234 -11.148134 2.141822e-08 8.082459e-07 9.753268 1182 Mir215
+
+Dnm3os Dnm3os -3.363344 5.8607432 -11.092261 2.283960e-08 8.082459e-07 9.689496 1401 Dnm3os
+
+Mir182 Mir182 4.903995 7.1511683 11.074468 2.331304e-08 8.082459e-07 9.658842 7189 Mir182
+
+Mir181a-2 Mir181a-2 -3.048298 6.9414651 -11.072128 2.337609e-08 8.082459e-07 9.644017 2817 Mir181a-2
+
+Mir1948 Mir1948 7.195525 4.5513493 11.005492 2.524936e-08 8.473388e-07 9.341794 2404 Mir1948
+
+Mir214 Mir214 -3.280874 5.4784451 -10.768257 3.332555e-08 1.086413e-06 9.318504 1048 Mir214
+
+Mir153 Mir153 -5.963803 1.4386315 -10.727082 3.498742e-08 1.093990e-06 9.035569 140 Mir153
+
+Cyp3a25 Cyp3a25 6.318200 1.4888933 10.698226 3.620443e-08 1.093990e-06 9.024973 226 Cyp3a25
+
+Gm5441 Gm5441 -5.982176 1.4484953 -10.692891 3.643436e-08 1.093990e-06 9.000362 142 Gm5441
+
+Mir125b-2 Mir125b-2 -3.077678 7.4316058 -10.446668 4.893073e-08 1.431538e-06 8.884250 3837 Mir125b-2
+
+Mir133a-1 Mir133a-1 -5.144671 0.5903264 -10.358205 5.447229e-08 1.553822e-06 8.575535 60 Mir133a-1
+
+1110038B12Rik 1110038B12Rik 2.226702 10.8487089 10.194609 6.655312e-08 1.852125e-06 8.439308 37066 1110038B12Rik
+
+Mir132 Mir132 -2.847559 5.3211839 -10.110952 7.380297e-08 2.004981e-06 8.531491 857 Mir132
+
+Rabggtb Rabggtb 1.935779 9.9874171 9.928995 9.262821e-08 2.457879e-06 8.133384 19535 Rabggtb
+
+Mir504 Mir504 -5.256127 0.6221088 -9.892894 9.693595e-08 2.513725e-06 8.068853 69 Mir504
+
+Mir150 Mir150 -2.938531 7.6297870 -9.842102 1.033602e-07 2.620755e-06 8.116464 4229 Mir150
+
+Mir199b Mir199b -5.752816 2.8805143 -9.823920 1.057683e-07 2.623514e-06 7.979387 370 Mir199b
+
+Mir23b Mir23b -2.124129 9.8141190 -9.806316 1.081569e-07 2.625681e-06 7.979464 16387 Mir23b
+
+Mir24-2 Mir24-2 -2.833979 7.3083691 -9.767192 1.136724e-07 2.646944e-06 8.030550 3470 Mir24-2
+
+Mir3074-2 Mir3074-2 -2.833979 7.3083691 -9.767192 1.136724e-07 2.646944e-06 8.030550 3470 Mir3074-2
+
+Mir155 Mir155 -3.906600 3.9899000 -9.732173 1.188627e-07 2.712448e-06 8.046518 463 Mir155
+
+
+
+
+
edgeR images and outputs
+(Click on a thumbnail image to download the corresponding original PDF image)
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
edgeR log output
+
+
+
+[1] prior.df = 8
+
+[1] "No GLM fit outlier genes found\n"
+
+[1] Common Dispersion = 0.228651460998105 CV = 0.478175136323613 getPriorN = 3.33333333333333
+
+[1] heart liver
+
+[1] "Raw sample read totals 2443751,1644652,1682104,1806045,1440960,1341813,2888924,1428365"
+
+[1] raw contig counts by sample:
+
+ liver_X11706Liv_CAAA liver_X11700Liv_ATTC liver_X11698Liv_ACTG liver_X11699Liv_ATGA heart_X11706He_AGTTC heart_X11699He_GGCTA heart_X11698He_TAGCT heart_X11700He_CTTGT
+
+ Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043
+
+ 1st Qu.:0.3032 1st Qu.:0.0043 1st Qu.:0.3032 1st Qu.:0.0043 1st Qu.:0.0043 1st Qu.:0.0043 1st Qu.:0.0043 1st Qu.:0.0043
+
+ Median :0.7789 Median :0.6031 Median :0.6998 Median :0.6031 Median :0.4786 Median :0.4786 Median :0.4786 Median :0.4786
+
+ Mean :1.0519 Mean :1.0343 Mean :0.9855 Mean :0.9966 Mean :0.9210 Mean :0.9428 Mean :1.0205 Mean :0.9753
+
+ 3rd Qu.:1.5410 3rd Qu.:1.6335 3rd Qu.:1.4473 3rd Qu.:1.5534 3rd Qu.:1.5770 3rd Qu.:1.5855 3rd Qu.:1.7161 3rd Qu.:1.6022
+
+ Max. :5.8209 Max. :5.6905 Max. :5.7999 Max. :5.7215 Max. :5.3609 Max. :5.3589 Max. :5.6967 Max. :5.3702
+
+ NA's :650 NA's :969 NA's :664 NA's :886 NA's :902 NA's :957 NA's :821 NA's :950
+
+[1] normalised contig counts by sample:
+
+ liver_X11706Liv_CAAA liver_X11700Liv_ATTC liver_X11698Liv_ACTG liver_X11699Liv_ATGA heart_X11706He_AGTTC heart_X11699He_GGCTA heart_X11698He_TAGCT heart_X11700He_CTTGT
+
+ Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf
+
+ 1st Qu.: 0 1st Qu.:-Inf 1st Qu.: 0 1st Qu.:-Inf 1st Qu.:-Inf 1st Qu.:-Inf 1st Qu.:-Inf 1st Qu.:-Inf
+
+ Median : 0 Median : 0 Median : 0 Median : 0 Median : 0 Median : 0 Median : 0 Median : 0
+
+ Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf
+
+ 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1
+
+ Max. : 6 Max. : 6 Max. : 6 Max. : 5 Max. : 5 Max. : 5 Max. : 6 Max. : 5
+
+[1] Using ncol rawrs= 8
+
+[1] # edgeR Top tags\n
+
+ Name logFC logCPM LR PValue adj.p.value Dispersion totreads URL
+
+Mir208a Mir208a -11.840751 8.465017 594.16946 3.104543e-131 3.542284e-128 0.05171220 4638 Mir208a
+
+Mir149 Mir149 -7.008984 8.861767 484.30321 2.473909e-107 1.411365e-104 0.04959937 6164 Mir149
+
+Mir208b Mir208b -13.291635 9.905945 417.69758 7.737463e-93 2.942815e-90 0.10508096 14756 Mir208b
+
+Mir122a Mir122a 10.514683 12.478088 415.17429 2.740525e-92 7.817349e-90 0.10803882 90428 Mir122a
+
+Mir204 Mir204 -7.498162 7.634507 341.30678 3.313430e-76 7.561247e-74 0.06907958 2601 Mir204
+
+Mir499 Mir499 -13.577454 8.700078 325.79199 7.930755e-73 1.508165e-70 0.12042284 6527 Mir499
+
+Mir490 Mir490 -8.534394 6.991023 303.17184 6.710366e-68 1.093790e-65 0.07949711 1741 Mir490
+
+Mir192 Mir192 6.953853 17.169364 217.22867 3.638307e-49 5.189135e-47 0.12700995 2325567 Mir192
+
+Mir802 Mir802 11.440805 6.593380 212.88059 3.231644e-48 4.097007e-46 0.12273671 1514 Mir802
+
+Mir1948 Mir1948 7.418142 7.252734 195.66958 1.840248e-44 2.099723e-42 0.12060221 2404 Mir1948
+
+Mir194-2 Mir194-2 5.298950 7.811522 191.85588 1.250960e-43 1.297587e-41 0.08670751 3570 Mir194-2
+
+Mir23a Mir23a -3.153807 9.529402 177.53185 1.676248e-40 1.593833e-38 0.04442763 10118 Mir23a
+
+Mir181c Mir181c -3.767686 10.639598 169.87390 7.883295e-39 6.919107e-37 0.06368883 23605 Mir181c
+
+Mir3073 Mir3073 10.686337 5.859950 164.86740 9.778593e-38 7.969554e-36 0.14069249 904 Mir3073
+
+Mir181d Mir181d -3.643963 7.300371 162.18591 3.767663e-37 2.865936e-35 0.05729574 2139 Mir181d
+
+Mir195 Mir195 -3.203683 8.215089 150.20548 1.563314e-34 1.114838e-32 0.05235020 3962 Mir195
+
+Mir10b Mir10b -5.182616 13.946466 147.24793 6.926819e-34 4.649118e-32 0.12268790 197340 Mir10b
+
+Mir101b Mir101b 3.759962 11.863187 136.31359 1.703812e-31 1.080028e-29 0.07961343 59019 Mir101b
+
+Mir378 Mir378 -3.115599 8.119617 126.76408 2.092233e-29 1.256441e-27 0.05942391 4075 Mir378
+
+Mir27a Mir27a -3.064687 10.642480 124.98911 5.117477e-29 2.919520e-27 0.06113852 21886 Mir27a
+
+Mir182 Mir182 5.057509 8.846381 123.17765 1.275060e-28 6.927826e-27 0.13653707 7189 Mir182
+
+Mir322 Mir322 -3.194159 9.012888 107.34926 3.732413e-25 1.935765e-23 0.07536483 7074 Mir322
+
+Mir199b Mir199b -5.520119 4.792610 102.10724 5.259607e-24 2.609223e-22 0.13417024 370 Mir199b
+
+Mir181a-2 Mir181a-2 -3.000177 7.637692 101.38361 7.578821e-24 3.603098e-22 0.06896654 2817 Mir181a-2
+
+Mir125b-2 Mir125b-2 -2.987759 8.144514 91.72544 9.957640e-22 4.488356e-20 0.07737381 3837 Mir125b-2
+
+Dnm3os Dnm3os -3.331215 6.686950 91.67250 1.022763e-21 4.488356e-20 0.08810497 1401 Dnm3os
+
+Mir184 Mir184 -5.111350 4.234160 84.35542 4.133639e-20 1.686711e-18 0.13502324 247 Mir184
+
+Mir215 Mir215 -3.058208 6.447966 84.35278 4.139167e-20 1.686711e-18 0.08138517 1182 Mir215
+
+Mir133b Mir133b -8.383611 3.584760 83.96681 5.031517e-20 1.960318e-18 0.17482280 159 Mir133b
+
+Mir150 Mir150 -2.883446 8.307765 83.91918 5.154210e-20 1.960318e-18 0.08008123 4229 Mir150
+
+Mir3074-2 Mir3074-2 -2.778308 7.935651 83.74839 5.619282e-20 2.040616e-18 0.07424646 3470 Mir3074-2
+
+Mir24-2 Mir24-2 -2.778307 7.935651 83.71222 5.723024e-20 2.040616e-18 0.07427992 3470 Mir24-2
+
+Mir193 Mir193 5.176579 4.801090 83.19222 7.445011e-20 2.574169e-18 0.14794861 421 Mir193
+
+Scarna17 Scarna17 2.182159 9.244479 81.91330 1.421894e-19 4.771710e-18 0.04982909 9224 Scarna17
+
+Mir214 Mir214 -3.271172 6.271755 80.43948 2.997458e-19 9.771712e-18 0.09566584 1048 Mir214
+
+Snord104 Snord104 2.330488 11.053611 79.50529 4.809369e-19 1.524303e-17 0.05915990 33458 Snord104
+
+Mir200a Mir200a 7.201555 4.139422 77.35503 1.428304e-18 4.365755e-17 0.19287764 264 Mir200a
+
+Mir200b Mir200b 6.525423 5.752604 77.31985 1.453976e-18 4.365755e-17 0.26237966 888 Mir200b
+
+Mir21 Mir21 2.923147 13.825255 75.51798 3.620938e-18 1.059357e-16 0.09395834 229120 Mir21
+
+Mir203 Mir203 1.956427 8.767610 75.17870 4.299815e-18 1.226522e-16 0.04381710 6739 Mir203
+
+Mir155 Mir155 -3.886731 5.068563 73.81316 8.587210e-18 2.389758e-16 0.12522673 463 Mir155
+
+Cyp3a25 Cyp3a25 8.681501 3.972085 72.29680 1.851471e-17 5.029829e-16 0.23125383 226 Cyp3a25
+
+Rabggtb Rabggtb 1.934093 10.298211 72.02043 2.129809e-17 5.651422e-16 0.04596646 19535 Rabggtb
+
+Mir23b Mir23b -2.100584 10.184110 71.44225 2.854935e-17 7.403367e-16 0.05416378 16387 Mir23b
+
+Snord52 Snord52 2.207491 10.217554 71.27974 3.100027e-17 7.860292e-16 0.05941483 18059 Snord52
+
+Gm5441 Gm5441 -6.881248 3.538457 70.05615 5.764004e-17 1.429724e-15 0.20097284 142 Gm5441
+
+Mir153 Mir153 -6.857671 3.517446 69.37600 8.137282e-17 1.975455e-15 0.20158808 140 Mir153
+
+Mir132 Mir132 -2.858294 5.938312 64.52507 9.531204e-16 2.265647e-14 0.09274248 857 Mir132
+
+1110038B12Rik 1110038B12Rik 2.195962 11.253090 62.92015 2.152583e-15 5.012443e-14 0.06712174 37066 1110038B12Rik
+
+Snord91a Snord91a 2.654072 6.557504 62.40549 2.795431e-15 6.379174e-14 0.08637410 1437 Snord91a
+
+[1] # 416 tags significant at adj p= 0.05
+
+
+
+
+
Other images and outputs
+(Click on a thumbnail image to download the corresponding original PDF image)
+
+
+
Other log output
+
+
+
+## Toolfactory generated command line = Rscript - None None
+
+Got TCols=1 5 6 7; CCols=2 3 4 8
+
+[1] # Quantiles for non-zero row counts:
+
+ 0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%
+
+ 1.0 1.0 2.0 3.0 4.0 8.0 13.0 24.0 86.6 753.0 2325567.0
+
+[1] Read 3242 contigs. Removed 1494 with no reads. After filtering at count quantile =0.3, there are 1141 contigs
+
+[1] "@@ using genecards substitution for urls"
+
+[1] # urls
+
+[1] 0610005C13Rik 0610007N19Rik 0610008F07Rik 0610009L18Rik 0610012G03Rik
+
+[6] 0610031O16Rik
+
+[1] # Total low count contigs per sample = 170,67,203,86,145,111,155,120
+
+[1] Using samples: liver_X11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam,liver_X11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam,liver_X11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam,liver_X11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam,heart_X11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam,heart_X11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam,heart_X11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam,heart_X11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam
+
+[1] Using design matrix:
+
+ (Intercept) groupliver
+
+1 1 1
+
+2 1 1
+
+3 1 1
+
+4 1 1
+
+5 1 0
+
+6 1 0
+
+7 1 0
+
+8 1 0
+
+attr(,"assign")
+
+[1] 0 1
+
+attr(,"contrasts")
+
+attr(,"contrasts")$group
+
+[1] contr.treatment
+
+R version 3.0.1 (2013-05-16)
+
+Platform: x86_64-unknown-linux-gnu (64-bit)
+
+locale:
+
+ [1] LC_CTYPE=en_AU.UTF-8 LC_NUMERIC=C LC_TIME=en_AU.UTF-8 LC_COLLATE=en_AU.UTF-8 LC_MONETARY=en_AU.UTF-8 LC_MESSAGES=en_AU.UTF-8 LC_PAPER=C LC_NAME=C LC_ADDRESS=C LC_TELEPHONE=C LC_MEASUREMENT=en_AU.UTF-8 LC_IDENTIFICATION=C
+
+attached base packages:
+
+ [1] parallel splines methods grid stats graphics grDevices utils datasets base
+
+other attached packages:
+
+ [1] RColorBrewer_1.0-5 DESeq2_1.0.18 RcppArmadillo_0.3.900.7 Rcpp_0.10.4 lattice_0.20-15 Biobase_2.20.1 GenomicRanges_1.12.4 IRanges_1.18.2 BiocGenerics_0.6.0 edgeR_3.2.4 limma_3.16.7 gplots_2.11.3 MASS_7.3-28 KernSmooth_2.23-10 caTools_1.14 gdata_2.13.2 gtools_3.0.0 stringr_0.6.2
+
+loaded via a namespace (and not attached):
+
+ [1] annotate_1.38.0 AnnotationDbi_1.22.6 bitops_1.0-5 DBI_0.2-7 genefilter_1.42.0 locfit_1.5-9.1 RSQLite_0.11.4 stats4_3.0.1 survival_2.37-4 XML_3.98-1.1 xtable_1.7-1
+
+
+
+
+
All output files available for downloading
+
+
+
+
diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/test-data/edgeRtest1out.xls
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/test-data/edgeRtest1out.xls Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,1142 @@
+ID logFC AveExpr t P.Value adj.P.Val B NReads URL
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diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/test-data/gentestdata.sh
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/test-data/gentestdata.sh Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,9 @@
+#!/bin/bash
+# generate test data for rgGSEA
+# ross lazarus June 2013
+# adjust gseajar_path !
+GSEAJAR_PATH=/home/rlazarus/galaxy-central/tool_dependency_dir/gsea_jar/2.0.12/fubar/rg_gsea_test/8e291f464aa0/jars/gsea2-2.0.12.jar
+python ../rgGSEA.py --input_tab "gsea_test_DGE.xls" --adjpvalcol "5" --signcol "2" --idcol "1" --outhtml "gseatestout.html" --input_name "gsea_test" --setMax "500" --setMin "15" --nPerm "10" --plotTop "20" --gsea_jar "$GSEAJAR_PATH" --output_dir "gseatestout" --mode "Max_probe"
+--title "GSEA test" --builtin_gmt "gseatestdata.gmt"
+
+
diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/test-data/test_bams2mx.xls
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/test-data/test_bams2mx.xls Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,3243 @@
+Contigname 11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam 11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam 11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam 11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam 11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam 11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam 11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam 11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam
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diff -r 37b851eb8203 -r 48d71bd383a1 differential_count_models/tool_dependencies.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/differential_count_models/tool_dependencies.xml Wed Aug 07 01:58:28 2013 -0400
@@ -0,0 +1,35 @@
+
+
+
+
+ package_ghostscript_9_07
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ $INSTALL_DIR
+ echo "source('http://bioconductor.org/biocLite.R')" > $INSTALL_DIR/runme.R
+ echo "installme=c('edgeR','limma','DESeq','DESeq2')" >> $INSTALL_DIR/runme.R
+ echo "biocLite()" >> $INSTALL_DIR/runme.R
+ echo "biocLite(installme)" >> $INSTALL_DIR/runme.R
+ echo "install.packages(c('stringr','gplots'),dependencies=T,repos='http://cran.us.r-project.org')" >> $INSTALL_DIR/runme.R
+ echo "quit(save='no')" >> $INSTALL_DIR/runme.R
+ export PATH=$PATH && export R_HOME=$R_HOME && export R_LIBS=$R_LIBS && R CMD BATCH $INSTALL_DIR/runme.R
+
+
+ Installs some basic bioc packages for the edgeR wrapper and dependencies graphicsmagick (replaces imagemagick) and ghostscript for compressing R's bloated pdfs
+ It's clunky but this is the most convenient way I could get anything installed into the package_r3
+ Note we use cran at fred hutch since no fastest mirror thingy
+
+
+
diff -r 37b851eb8203 -r 48d71bd383a1 rgedgeR/rgToolFactory.py
--- a/rgedgeR/rgToolFactory.py Sat Jul 27 22:28:00 2013 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,605 +0,0 @@
-# rgToolFactory.py
-# see https://bitbucket.org/fubar/galaxytoolfactory/wiki/Home
-#
-# copyright ross lazarus (ross stop lazarus at gmail stop com) May 2012
-#
-# all rights reserved
-# Licensed under the LGPL
-# suggestions for improvement and bug fixes welcome at https://bitbucket.org/fubar/galaxytoolfactory/wiki/Home
-#
-# july 2013
-# added ability to combine images and individual log files into html output
-# just make sure there's a log file foo.log and it will be output
-# together with all images named like "foo_*.pdf
-# otherwise old format for html
-#
-# January 2013
-# problem pointed out by Carlos Borroto
-# added escaping for <>$ - thought I did that ages ago...
-#
-# August 11 2012
-# changed to use shell=False and cl as a sequence
-
-# This is a Galaxy tool factory for simple scripts in python, R or whatever ails ye.
-# It also serves as the wrapper for the new tool.
-#
-# you paste and run your script
-# Only works for simple scripts that read one input from the history.
-# Optionally can write one new history dataset,
-# and optionally collect any number of outputs into links on an autogenerated HTML page.
-
-# DO NOT install on a public or important site - please.
-
-# installed generated tools are fine if the script is safe.
-# They just run normally and their user cannot do anything unusually insecure
-# but please, practice safe toolshed.
-# Read the fucking code before you install any tool
-# especially this one
-
-# After you get the script working on some test data, you can
-# optionally generate a toolshed compatible gzip file
-# containing your script safely wrapped as an ordinary Galaxy script in your local toolshed for
-# safe and largely automated installation in a production Galaxy.
-
-# If you opt for an HTML output, you get all the script outputs arranged
-# as a single Html history item - all output files are linked, thumbnails for all the pdfs.
-# Ugly but really inexpensive.
-#
-# Patches appreciated please.
-#
-#
-# long route to June 2012 product
-# Behold the awesome power of Galaxy and the toolshed with the tool factory to bind them
-# derived from an integrated script model
-# called rgBaseScriptWrapper.py
-# Note to the unwary:
-# This tool allows arbitrary scripting on your Galaxy as the Galaxy user
-# There is nothing stopping a malicious user doing whatever they choose
-# Extremely dangerous!!
-# Totally insecure. So, trusted users only
-#
-# preferred model is a developer using their throw away workstation instance - ie a private site.
-# no real risk. The universe_wsgi.ini admin_users string is checked - only admin users are permitted to run this tool.
-#
-
-import sys
-import shutil
-import subprocess
-import os
-import time
-import tempfile
-import optparse
-import tarfile
-import re
-import shutil
-import math
-
-progname = os.path.split(sys.argv[0])[1]
-myversion = 'V000.2 June 2012'
-verbose = False
-debug = False
-toolFactoryURL = 'https://bitbucket.org/fubar/galaxytoolfactory'
-
-def timenow():
- """return current time as a string
- """
- return time.strftime('%d/%m/%Y %H:%M:%S', time.localtime(time.time()))
-
-html_escape_table = {
- "&": "&",
- ">": ">",
- "<": "<",
- "$": "\$"
- }
-
-def html_escape(text):
- """Produce entities within text."""
- return "".join(html_escape_table.get(c,c) for c in text)
-
-def cmd_exists(cmd):
- return subprocess.call("type " + cmd, shell=True,
- stdout=subprocess.PIPE, stderr=subprocess.PIPE) == 0
-
-
-class ScriptRunner:
- """class is a wrapper for an arbitrary script
- """
-
- def __init__(self,opts=None,treatbashSpecial=True):
- """
- cleanup inputs, setup some outputs
-
- """
- self.useGM = cmd_exists('gm')
- self.useIM = cmd_exists('convert')
- self.useGS = cmd_exists('gs')
- self.treatbashSpecial = treatbashSpecial
- if opts.output_dir: # simplify for the tool tarball
- os.chdir(opts.output_dir)
- self.thumbformat = 'png'
- self.opts = opts
- self.toolname = re.sub('[^a-zA-Z0-9_]+', '', opts.tool_name) # a sanitizer now does this but..
- self.toolid = self.toolname
- self.myname = sys.argv[0] # get our name because we write ourselves out as a tool later
- self.pyfile = self.myname # crude but efficient - the cruft won't hurt much
- self.xmlfile = '%s.xml' % self.toolname
- s = open(self.opts.script_path,'r').readlines()
- s = [x.rstrip() for x in s] # remove pesky dos line endings if needed
- self.script = '\n'.join(s)
- fhandle,self.sfile = tempfile.mkstemp(prefix=self.toolname,suffix=".%s" % (opts.interpreter))
- tscript = open(self.sfile,'w') # use self.sfile as script source for Popen
- tscript.write(self.script)
- tscript.close()
- self.indentedScript = '\n'.join([' %s' % x for x in s]) # for restructured text in help
- self.escapedScript = '\n'.join([html_escape(x) for x in s])
- self.elog = os.path.join(self.opts.output_dir,"%s_error.log" % self.toolname)
- if opts.output_dir: # may not want these complexities
- self.tlog = os.path.join(self.opts.output_dir,"%s_runner.log" % self.toolname)
- art = '%s.%s' % (self.toolname,opts.interpreter)
- artpath = os.path.join(self.opts.output_dir,art) # need full path
- artifact = open(artpath,'w') # use self.sfile as script source for Popen
- artifact.write(self.script)
- artifact.close()
- self.cl = []
- self.html = []
- a = self.cl.append
- a(opts.interpreter)
- if self.treatbashSpecial and opts.interpreter in ['bash','sh']:
- a(self.sfile)
- else:
- a('-') # stdin
- a(opts.input_tab)
- a(opts.output_tab)
- self.outFormats = 'tabular' # TODO make this an option at tool generation time
- self.inputFormats = 'tabular' # TODO make this an option at tool generation time
- self.test1Input = '%s_test1_input.xls' % self.toolname
- self.test1Output = '%s_test1_output.xls' % self.toolname
- self.test1HTML = '%s_test1_output.html' % self.toolname
-
- def makeXML(self):
- """
- Create a Galaxy xml tool wrapper for the new script as a string to write out
- fixme - use templating or something less fugly than this example of what we produce
-
-
- a tabular file
-
- reverse.py --script_path "$runMe" --interpreter "python"
- --tool_name "reverse" --input_tab "$input1" --output_tab "$tab_file"
-
-
-
-
-
-
-
-
-
-
-
-**What it Does**
-
-Reverse the columns in a tabular file
-
-
-
-
-
-# reverse order of columns in a tabular file
-import sys
-inp = sys.argv[1]
-outp = sys.argv[2]
-i = open(inp,'r')
-o = open(outp,'w')
-for row in i:
- rs = row.rstrip().split('\t')
- rs.reverse()
- o.write('\t'.join(rs))
- o.write('\n')
-i.close()
-o.close()
-
-
-
-
-
-
- """
- newXML="""
- %(tooldesc)s
- %(command)s
-
- %(inputs)s
-
-
- %(outputs)s
-
-
-
- %(script)s
-
-
- %(tooltests)s
-
- %(help)s
-
- """ # needs a dict with toolname, toolid, interpreter, scriptname, command, inputs as a multi line string ready to write, outputs ditto, help ditto
-
- newCommand="""
- %(toolname)s.py --script_path "$runMe" --interpreter "%(interpreter)s"
- --tool_name "%(toolname)s" %(command_inputs)s %(command_outputs)s
- """ # may NOT be an input or htmlout
- tooltestsTabOnly = """
-
-
-
-
- """
- tooltestsHTMLOnly = """
-
-
-
-
- """
- tooltestsBoth = """
-
-
-
-
-
- """
- xdict = {}
- xdict['tool_version'] = self.opts.tool_version
- xdict['test1Input'] = self.test1Input
- xdict['test1HTML'] = self.test1HTML
- xdict['test1Output'] = self.test1Output
- if self.opts.make_HTML and self.opts.output_tab <> 'None':
- xdict['tooltests'] = tooltestsBoth % xdict
- elif self.opts.make_HTML:
- xdict['tooltests'] = tooltestsHTMLOnly % xdict
- else:
- xdict['tooltests'] = tooltestsTabOnly % xdict
- xdict['script'] = self.escapedScript
- # configfile is least painful way to embed script to avoid external dependencies
- # but requires escaping of <, > and $ to avoid Mako parsing
- if self.opts.help_text:
- xdict['help'] = open(self.opts.help_text,'r').read()
- else:
- xdict['help'] = 'Please ask the tool author for help as none was supplied at tool generation'
- coda = ['**Script**','Pressing execute will run the following code over your input file and generate some outputs in your history::']
- coda.append(self.indentedScript)
- coda.append('**Attribution** This Galaxy tool was created by %s at %s\nusing the Galaxy Tool Factory.' % (self.opts.user_email,timenow()))
- coda.append('See %s for details of that project' % (toolFactoryURL))
- coda.append('Please cite: Creating re-usable tools from scripts: The Galaxy Tool Factory. Ross Lazarus; Antony Kaspi; Mark Ziemann; The Galaxy Team. ')
- coda.append('Bioinformatics 2012; doi: 10.1093/bioinformatics/bts573')
- xdict['help'] = '%s\n%s' % (xdict['help'],'\n'.join(coda))
- if self.opts.tool_desc:
- xdict['tooldesc'] = '%s ' % self.opts.tool_desc
- else:
- xdict['tooldesc'] = ''
- xdict['command_outputs'] = ''
- xdict['outputs'] = ''
- if self.opts.input_tab <> 'None':
- xdict['command_inputs'] = '--input_tab "$input1" ' # the space may matter a lot if we append something
- xdict['inputs'] = ' \n' % self.inputFormats
- else:
- xdict['command_inputs'] = '' # assume no input - eg a random data generator
- xdict['inputs'] = ''
- xdict['inputs'] += ' \n' % self.toolname
- xdict['toolname'] = self.toolname
- xdict['toolid'] = self.toolid
- xdict['interpreter'] = self.opts.interpreter
- xdict['scriptname'] = self.sfile
- if self.opts.make_HTML:
- xdict['command_outputs'] += ' --output_dir "$html_file.files_path" --output_html "$html_file" --make_HTML "yes" '
- xdict['outputs'] += ' \n'
- if self.opts.output_tab <> 'None':
- xdict['command_outputs'] += ' --output_tab "$tab_file"'
- xdict['outputs'] += ' \n' % self.outFormats
- xdict['command'] = newCommand % xdict
- xmls = newXML % xdict
- xf = open(self.xmlfile,'w')
- xf.write(xmls)
- xf.write('\n')
- xf.close()
- # ready for the tarball
-
-
- def makeTooltar(self):
- """
- a tool is a gz tarball with eg
- /toolname/tool.xml /toolname/tool.py /toolname/test-data/test1_in.foo ...
- """
- retval = self.run()
- if retval:
- print >> sys.stderr,'## Run failed. Cannot build yet. Please fix and retry'
- sys.exit(1)
- self.makeXML()
- tdir = self.toolname
- os.mkdir(tdir)
- if self.opts.input_tab <> 'None': # no reproducible test otherwise? TODO: maybe..
- testdir = os.path.join(tdir,'test-data')
- os.mkdir(testdir) # make tests directory
- shutil.copyfile(self.opts.input_tab,os.path.join(testdir,self.test1Input))
- if self.opts.output_tab <> 'None':
- shutil.copyfile(self.opts.output_tab,os.path.join(testdir,self.test1Output))
- if self.opts.make_HTML:
- shutil.copyfile(self.opts.output_html,os.path.join(testdir,self.test1HTML))
- if self.opts.output_dir:
- shutil.copyfile(self.tlog,os.path.join(testdir,'test1_out.log'))
- op = '%s.py' % self.toolname # new name
- outpiname = os.path.join(tdir,op) # path for the tool tarball
- pyin = os.path.basename(self.pyfile) # our name - we rewrite ourselves (TM)
- notes = ['# %s - a self annotated version of %s generated by running %s\n' % (op,pyin,pyin),]
- notes.append('# to make a new Galaxy tool called %s\n' % self.toolname)
- notes.append('# User %s at %s\n' % (self.opts.user_email,timenow()))
- pi = open(self.pyfile,'r').readlines() # our code becomes new tool wrapper (!) - first Galaxy worm
- notes += pi
- outpi = open(outpiname,'w')
- outpi.write(''.join(notes))
- outpi.write('\n')
- outpi.close()
- stname = os.path.join(tdir,self.sfile)
- if not os.path.exists(stname):
- shutil.copyfile(self.sfile, stname)
- xtname = os.path.join(tdir,self.xmlfile)
- if not os.path.exists(xtname):
- shutil.copyfile(self.xmlfile,xtname)
- tarpath = "%s.gz" % self.toolname
- tar = tarfile.open(tarpath, "w:gz")
- tar.add(tdir,arcname=self.toolname)
- tar.close()
- shutil.copyfile(tarpath,self.opts.new_tool)
- shutil.rmtree(tdir)
- ## TODO: replace with optional direct upload to local toolshed?
- return retval
-
-
- def compressPDF(self,inpdf=None,thumbformat='png'):
- """need absolute path to pdf
- """
- assert os.path.isfile(inpdf), "## Input %s supplied to %s compressPDF not found" % (inpdf,self.myName)
- hf,hlog = tempfile.mkstemp(suffix="%s.log" % self.toolname)
- sto = open(hlog,'w')
- outpdf = '%s_compressed' % inpdf
- cl = ["gs", "-sDEVICE=pdfwrite", "-dNOPAUSE", "-dBATCH","-dPDFSETTINGS=/printer", "-sOutputFile=%s" % outpdf,inpdf]
- x = subprocess.Popen(cl,stdout=sto,stderr=sto,cwd=self.opts.output_dir)
- retval1 = x.wait()
- if retval1 == 0:
- os.unlink(inpdf)
- shutil.move(outpdf,inpdf)
- outpng = '%s.%s' % (os.path.splitext(inpdf)[0],thumbformat)
- if self.useGM:
- cl2 = ['gm convert', inpdf, outpng]
- else: # assume imagemagick
- cl2 = ['convert', inpdf, outpng]
- x = subprocess.Popen(cl2,stdout=sto,stderr=sto,cwd=self.opts.output_dir)
- retval2 = x.wait()
- sto.close()
- retval = retval1 or retval2
- return retval
-
-
- def getfSize(self,fpath,outpath):
- """
- format a nice file size string
- """
- size = ''
- fp = os.path.join(outpath,fpath)
- if os.path.isfile(fp):
- size = '0 B'
- n = float(os.path.getsize(fp))
- if n > 2**20:
- size = '%1.1f MB' % (n/2**20)
- elif n > 2**10:
- size = '%1.1f KB' % (n/2**10)
- elif n > 0:
- size = '%d B' % (int(n))
- return size
-
- def makeHtml(self):
- """ Create an HTML file content to list all the artifacts found in the output_dir
- """
-
- galhtmlprefix = """
-
-
-
-
-
-
-
-
- """
- galhtmlattr = """
"""
- galhtmlpostfix = """
\n"""
-
- flist = os.listdir(self.opts.output_dir)
- flist = [x for x in flist if x <> 'Rplots.pdf']
- flist.sort()
- html = []
- html.append(galhtmlprefix % progname)
- html.append('Galaxy Tool "%s" run at %s
' % (self.toolname,timenow()))
- fhtml = []
- if len(flist) > 0:
- logfiles = [x for x in flist if x.lower().endswith('.log')] # log file names determine sections
- logfiles.sort()
- logfiles = [x for x in logfiles if os.path.abspath(x) <> os.path.abspath(self.tlog)]
- logfiles.append(os.path.abspath(self.tlog)) # make it the last one
- pdflist = []
- npdf = len([x for x in flist if os.path.splitext(x)[-1].lower() == '.pdf'])
- for rownum,fname in enumerate(flist):
- dname,e = os.path.splitext(fname)
- sfsize = self.getfSize(fname,self.opts.output_dir)
- if e.lower() == '.pdf' : # compress and make a thumbnail
- thumb = '%s.%s' % (dname,self.thumbformat)
- pdff = os.path.join(self.opts.output_dir,fname)
- retval = self.compressPDF(inpdf=pdff,thumbformat=self.thumbformat)
- if retval == 0:
- pdflist.append((fname,thumb))
- if (rownum+1) % 2 == 0:
- fhtml.append('%s %s ' % (fname,fname,sfsize))
- else:
- fhtml.append('%s %s ' % (fname,fname,sfsize))
- for logfname in logfiles: # expect at least tlog - if more
- if os.path.abspath(logfname) == os.path.abspath(self.tlog): # handled later
- sectionname = 'All tool run'
- if (len(logfiles) > 1):
- sectionname = 'Other'
- ourpdfs = pdflist
- else:
- realname = os.path.basename(logfname)
- sectionname = os.path.splitext(realname)[0].split('_')[0] # break in case _ added to log
- ourpdfs = [x for x in pdflist if os.path.basename(x[0]).split('_')[0] == sectionname]
- pdflist = [x for x in pdflist if os.path.basename(x[0]).split('_')[0] <> sectionname] # remove
- nacross = 1
- npdf = len(ourpdfs)
-
- if npdf > 0:
- nacross = math.sqrt(npdf) ## int(round(math.log(npdf,2)))
- if int(nacross)**2 != npdf:
- nacross += 1
- nacross = int(nacross)
- width = min(400,int(1200/nacross))
- html.append('%s images and outputs
' % sectionname)
- html.append('(Click on a thumbnail image to download the corresponding original PDF image) ')
- ntogo = nacross # counter for table row padding with empty cells
- html.append('\n')
- for i,paths in enumerate(ourpdfs):
- fname,thumb = paths
- s= """ \n""" % (fname,thumb,fname,width,fname)
- if ((i+1) % nacross == 0):
- s += ' \n'
- ntogo = 0
- if i < (npdf - 1): # more to come
- s += ''
- ntogo = nacross
- else:
- ntogo -= 1
- html.append(s)
- if html[-1].strip().endswith(' '):
- html.append('
\n')
- else:
- if ntogo > 0: # pad
- html.append(' '*ntogo)
- html.append('\n')
- logt = open(logfname,'r').readlines()
- logtext = [x for x in logt if x.strip() > '']
- html.append('%s log output
' % sectionname)
- if len(logtext) > 1:
- html.append('\n\n')
- html += logtext
- html.append('\n \n')
- else:
- html.append('%s is empty ' % logfname)
- if len(fhtml) > 0:
- fhtml.insert(0,'Output File Name (click to view) Size \n')
- fhtml.append('
')
- html.append('All output files available for downloading
\n')
- html += fhtml # add all non-pdf files to the end of the display
- else:
- html.append('### Error - %s returned no files - please confirm that parameters are sane
' % self.opts.interpreter)
- html.append(galhtmlpostfix)
- htmlf = file(self.opts.output_html,'w')
- htmlf.write('\n'.join(html))
- htmlf.write('\n')
- htmlf.close()
- self.html = html
-
-
- def run(self):
- """
- scripts must be small enough not to fill the pipe!
- """
- if self.treatbashSpecial and self.opts.interpreter in ['bash','sh']:
- retval = self.runBash()
- else:
- if self.opts.output_dir:
- ste = open(self.elog,'w')
- sto = open(self.tlog,'w')
- sto.write('## Toolfactory generated command line = %s\n' % ' '.join(self.cl))
- sto.flush()
- p = subprocess.Popen(self.cl,shell=False,stdout=sto,stderr=ste,stdin=subprocess.PIPE,cwd=self.opts.output_dir)
- else:
- p = subprocess.Popen(self.cl,shell=False,stdin=subprocess.PIPE)
- p.stdin.write(self.script)
- p.stdin.close()
- retval = p.wait()
- if self.opts.output_dir:
- sto.close()
- ste.close()
- err = open(self.elog,'r').readlines()
- if retval <> 0 and err: # problem
- print >> sys.stderr,err
- if self.opts.make_HTML:
- self.makeHtml()
- return retval
-
- def runBash(self):
- """
- cannot use - for bash so use self.sfile
- """
- if self.opts.output_dir:
- s = '## Toolfactory generated command line = %s\n' % ' '.join(self.cl)
- sto = open(self.tlog,'w')
- sto.write(s)
- sto.flush()
- p = subprocess.Popen(self.cl,shell=False,stdout=sto,stderr=sto,cwd=self.opts.output_dir)
- else:
- p = subprocess.Popen(self.cl,shell=False)
- retval = p.wait()
- if self.opts.output_dir:
- sto.close()
- if self.opts.make_HTML:
- self.makeHtml()
- return retval
-
-
-def main():
- u = """
- This is a Galaxy wrapper. It expects to be called by a special purpose tool.xml as:
- rgBaseScriptWrapper.py --script_path "$scriptPath" --tool_name "foo" --interpreter "Rscript"
-
- """
- op = optparse.OptionParser()
- a = op.add_option
- a('--script_path',default=None)
- a('--tool_name',default=None)
- a('--interpreter',default=None)
- a('--output_dir',default=None)
- a('--output_html',default=None)
- a('--input_tab',default="None")
- a('--output_tab',default="None")
- a('--user_email',default='Unknown')
- a('--bad_user',default=None)
- a('--make_Tool',default=None)
- a('--make_HTML',default=None)
- a('--help_text',default=None)
- a('--tool_desc',default=None)
- a('--new_tool',default=None)
- a('--tool_version',default=None)
- opts, args = op.parse_args()
- assert not opts.bad_user,'UNAUTHORISED: %s is NOT authorized to use this tool until Galaxy admin adds %s to admin_users in universe_wsgi.ini' % (opts.bad_user,opts.bad_user)
- assert opts.tool_name,'## Tool Factory expects a tool name - eg --tool_name=DESeq'
- assert opts.interpreter,'## Tool Factory wrapper expects an interpreter - eg --interpreter=Rscript'
- assert os.path.isfile(opts.script_path),'## Tool Factory wrapper expects a script path - eg --script_path=foo.R'
- if opts.output_dir:
- try:
- os.makedirs(opts.output_dir)
- except:
- pass
- r = ScriptRunner(opts)
- if opts.make_Tool:
- retcode = r.makeTooltar()
- else:
- retcode = r.run()
- os.unlink(r.sfile)
- if retcode:
- sys.exit(retcode) # indicate failure to job runner
-
-
-if __name__ == "__main__":
- main()
-
-
diff -r 37b851eb8203 -r 48d71bd383a1 rgedgeR/rgedgeRpaired.xml
--- a/rgedgeR/rgedgeRpaired.xml Sat Jul 27 22:28:00 2013 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,933 +0,0 @@
-
- models using BioConductor packages
-
- biocbasics
- r3
- graphicsmagick
- ghostscript
-
-
-
- rgToolFactory.py --script_path "$runme" --interpreter "Rscript" --tool_name "DifferentialCounts"
- --output_dir "$html_file.files_path" --output_html "$html_file" --make_HTML "yes"
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
- Do not run edgeR
- Run edgeR
-
-
-
-
-
-
-
-
- Do not run DESeq2
- Run DESeq2
-
-
-
- Parametric (default) fit for dispersions
- Local fit - this will automagically be used if parametric fit fails
- Mean dispersion fit- use this if you really understand what you're doing - read the fine manual linked below in the documentation
-
-
-
-
-
- Do not run VOOM
- Run VOOM
-
-
-
- fdr
- Benjamini Hochberg
- Benjamini Yukateli
- Bonferroni
- Hochberg
- Holm
- Hommel
- no control for multiple tests
-
-
-
-
- edgeR['doedgeR'] == "T"
-
-
- DESeq2['doDESeq2'] == "T"
-
-
- doVoom == "T"
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
- nsamp) {
- dm =dm[1:nsamp,]
- #sub = paste('Showing',nsamp,'contigs ranked for evidence for differential abundance out of',nprobes,'total')
- }
- newcolnames = substr(colnames(dm),1,20)
- colnames(dm) = newcolnames
- pdf(outpdfname)
- heatmap.2(dm,main=myTitle,ColSideColors=pcols,col=topo.colors(100),dendrogram="col",key=T,density.info='none',
- Rowv=F,scale='row',trace='none',margins=c(8,8),cexRow=0.4,cexCol=0.5)
- dev.off()
-}
-
-hmap = function(cmat,nmeans=4,outpdfname="heatMap.pdf",nsamp=250,TName='Treatment',group=NA,myTitle="Title goes here")
-{
- # for 2 groups only was
- #col.map = function(g) {if (g==TName) "#FF0000" else "#0000FF"}
- #pcols = unlist(lapply(group,col.map))
- gu = unique(group)
- colours = rainbow(length(gu),start=0.3,end=0.6)
- pcols = colours[match(group,gu)]
- nrows = nrow(cmat)
- mtitle = paste(myTitle,'Heatmap: n contigs =',nrows)
- if (nrows > nsamp) {
- cmat = cmat[c(1:nsamp),]
- mtitle = paste('Heatmap: Top ',nsamp,' DE contigs (of ',nrows,')',sep='')
- }
- newcolnames = substr(colnames(cmat),1,20)
- colnames(cmat) = newcolnames
- pdf(outpdfname)
- heatmap(cmat,scale='row',main=mtitle,cexRow=0.3,cexCol=0.4,Rowv=NA,ColSideColors=pcols)
- dev.off()
-}
-
-qqPlot = function(descr='qqplot',pvector, outpdf='qqplot.pdf',...)
-# stolen from https://gist.github.com/703512
-{
- o = -log10(sort(pvector,decreasing=F))
- e = -log10( 1:length(o)/length(o) )
- o[o==-Inf] = reallysmall
- o[o==Inf] = reallybig
- maint = descr
- pdf(outpdf)
- plot(e,o,pch=19,cex=1, main=maint, ...,
- xlab=expression(Expected~~-log[10](italic(p))),
- ylab=expression(Observed~~-log[10](italic(p))),
- xlim=c(0,max(e)), ylim=c(0,max(o)))
- lines(e,e,col="red")
- grid(col = "lightgray", lty = "dotted")
- dev.off()
-}
-
-smearPlot = function(DGEList,deTags, outSmear, outMain)
- {
- pdf(outSmear)
- plotSmear(DGEList,de.tags=deTags,main=outMain)
- grid(col="lightgray", lty="dotted")
- dev.off()
- }
-
-boxPlot = function(rawrs,cleanrs,maint,myTitle,pdfname)
-{ #
- nc = ncol(rawrs)
- for (i in c(1:nc)) {rawrs[(rawrs[,i] < 0),i] = NA}
- fullnames = colnames(rawrs)
- newcolnames = substr(colnames(rawrs),1,20)
- colnames(rawrs) = newcolnames
- newcolnames = substr(colnames(cleanrs),1,20)
- colnames(cleanrs) = newcolnames
- defpar = par(no.readonly=T)
- print.noquote('raw contig counts by sample:')
- print.noquote(summary(rawrs))
- print.noquote('normalised contig counts by sample:')
- print.noquote(summary(cleanrs))
- pdf(pdfname)
- par(mfrow=c(1,2))
- boxplot(rawrs,varwidth=T,notch=T,ylab='log contig count',col="maroon",las=3,cex.axis=0.35,main=paste('Raw:',maint))
- grid(col="lightgray",lty="dotted")
- boxplot(cleanrs,varwidth=T,notch=T,ylab='log contig count',col="maroon",las=3,cex.axis=0.35,main=paste('After ',maint))
- grid(col="lightgray",lty="dotted")
- dev.off()
- pdfname = "sample_counts_histogram.pdf"
- nc = ncol(rawrs)
- print.noquote(paste('Using ncol rawrs=',nc))
- ncroot = round(sqrt(nc))
- if (ncroot*ncroot < nc) { ncroot = ncroot + 1 }
- m = c()
- for (i in c(1:nc)) {
- rhist = hist(rawrs[,i],breaks=100,plot=F)
- m = append(m,max(rhist\$counts))
- }
- ymax = max(m)
- pdf(pdfname)
- par(mfrow=c(ncroot,ncroot))
- for (i in c(1:nc)) {
- hist(rawrs[,i], main=paste("Contig logcount",i), xlab='log raw count', col="maroon",
- breaks=100,sub=fullnames[i],cex=0.8,ylim=c(0,ymax))
- }
- dev.off()
- par(defpar)
-
-}
-
-cumPlot = function(rawrs,cleanrs,maint,myTitle)
-{ # updated to use ecdf
- pdfname = "Filtering_rowsum_bar_charts.pdf"
- defpar = par(no.readonly=T)
- lrs = log(rawrs,10)
- lim = max(lrs)
- pdf(pdfname)
- par(mfrow=c(2,1))
- hist(lrs,breaks=100,main=paste('Before:',maint),xlab="# Reads (log)",
- ylab="Count",col="maroon",sub=myTitle, xlim=c(0,lim),las=1)
- grid(col="lightgray", lty="dotted")
- lrs = log(cleanrs,10)
- hist(lrs,breaks=100,main=paste('After:',maint),xlab="# Reads (log)",
- ylab="Count",col="maroon",sub=myTitle,xlim=c(0,lim),las=1)
- grid(col="lightgray", lty="dotted")
- dev.off()
- par(defpar)
-}
-
-cumPlot1 = function(rawrs,cleanrs,maint,myTitle)
-{ # updated to use ecdf
- pdfname = paste(gsub(" ","", myTitle , fixed=TRUE),"RowsumCum.pdf",sep='_')
- pdf(pdfname)
- par(mfrow=c(2,1))
- lastx = max(rawrs)
- rawe = knots(ecdf(rawrs))
- cleane = knots(ecdf(cleanrs))
- cy = 1:length(cleane)/length(cleane)
- ry = 1:length(rawe)/length(rawe)
- plot(rawe,ry,type='l',main=paste('Before',maint),xlab="Log Contig Total Reads",
- ylab="Cumulative proportion",col="maroon",log='x',xlim=c(1,lastx),sub=myTitle)
- grid(col="blue")
- plot(cleane,cy,type='l',main=paste('After',maint),xlab="Log Contig Total Reads",
- ylab="Cumulative proportion",col="maroon",log='x',xlim=c(1,lastx),sub=myTitle)
- grid(col="blue")
- dev.off()
-}
-
-
-
-doGSEA = function(y=NULL,design=NULL,histgmt="",
- bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
- ntest=0, myTitle="myTitle", outfname="GSEA.xls", minnin=5, maxnin=2000,fdrthresh=0.05,fdrtype="BH")
-{
- sink('Camera.log')
- genesets = c()
- if (bigmt > "")
- {
- bigenesets = readLines(bigmt)
- genesets = bigenesets
- }
- if (histgmt > "")
- {
- hgenesets = readLines(histgmt)
- if (bigmt > "") {
- genesets = rbind(genesets,hgenesets)
- } else {
- genesets = hgenesets
- } # use only history if no bi
- }
- print.noquote(paste("@@@read",length(genesets), 'genesets from',histgmt,bigmt))
- genesets = strsplit(genesets,'\t') # tabular. genesetid\tURLorwhatever\tgene_1\t..\tgene_n
- outf = outfname
- head=paste(myTitle,'edgeR GSEA')
- write(head,file=outfname,append=F)
- ntest=length(genesets)
- urownames = toupper(rownames(y))
- upcam = c()
- downcam = c()
- for (i in 1:ntest) {
- gs = unlist(genesets[i])
- g = gs[1] # geneset_id
- u = gs[2]
- if (u > "") { u = paste("",u," ",sep="") }
- glist = gs[3:length(gs)] # member gene symbols
- glist = toupper(glist)
- inglist = urownames %in% glist
- nin = sum(inglist)
- if ((nin > minnin) && (nin < maxnin)) {
- ### print(paste('@@found',sum(inglist),'genes in glist'))
- camres = camera(y=y,index=inglist,design=design)
- if (! is.null(camres)) {
- rownames(camres) = g # gene set name
- camres = cbind(GeneSet=g,URL=u,camres)
- if (camres\$Direction == "Up")
- {
- upcam = rbind(upcam,camres) } else {
- downcam = rbind(downcam,camres)
- }
- }
- }
- }
- uscam = upcam[order(upcam\$PValue),]
- unadjp = uscam\$PValue
- uscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
- nup = max(10,sum((uscam\$adjPValue < fdrthresh)))
- dscam = downcam[order(downcam\$PValue),]
- unadjp = dscam\$PValue
- dscam\$adjPValue = p.adjust(unadjp,method=fdrtype)
- ndown = max(10,sum((dscam\$adjPValue < fdrthresh)))
- write.table(uscam,file=paste('camera_up',outfname,sep='_'),quote=F,sep='\t',row.names=F)
- write.table(dscam,file=paste('camera_down',outfname,sep='_'),quote=F,sep='\t',row.names=F)
- print.noquote(paste('@@@@@ Camera up top',nup,'gene sets:'))
- write.table(head(uscam,nup),file="",quote=F,sep='\t',row.names=F)
- print.noquote(paste('@@@@@ Camera down top',ndown,'gene sets:'))
- write.table(head(dscam,ndown),file="",quote=F,sep='\t',row.names=F)
- sink()
-}
-
-
-
-edgeIt = function (Count_Matrix=c(),group=c(),out_edgeR=F,out_VOOM=F,out_DESeq2=F,fdrtype='fdr',priordf=5,
- fdrthresh=0.05,outputdir='.', myTitle='Differential Counts',libSize=c(),useNDF=F,
- filterquantile=0.2, subjects=c(),mydesign=NULL,
- doDESeq2=T,doVoom=T,doCamera=T,doedgeR=T,org='hg19',
- histgmt="", bigmt="/data/genomes/gsea/3.1/Abetterchoice_nocgp_c2_c3_c5_symbols_all.gmt",
- doCook=F,DESeq_fitType="parameteric")
-{
- # Error handling
- if (length(unique(group))!=2){
- print("Number of conditions identified in experiment does not equal 2")
- q()
- }
- require(edgeR)
- options(width = 512)
- mt = paste(unlist(strsplit(myTitle,'_')),collapse=" ")
- allN = nrow(Count_Matrix)
- nscut = round(ncol(Count_Matrix)/2)
- colTotmillionreads = colSums(Count_Matrix)/1e6
- counts.dataframe = as.data.frame(c())
- rawrs = rowSums(Count_Matrix)
- nonzerod = Count_Matrix[(rawrs > 0),] # remove all zero count genes
- nzN = nrow(nonzerod)
- nzrs = rowSums(nonzerod)
- zN = allN - nzN
- print('# Quantiles for non-zero row counts:',quote=F)
- print(quantile(nzrs,probs=seq(0,1,0.1)),quote=F)
- if (useNDF == T)
- {
- gt1rpin3 = rowSums(Count_Matrix/expandAsMatrix(colTotmillionreads,dim(Count_Matrix)) >= 1) >= nscut
- lo = colSums(Count_Matrix[!gt1rpin3,])
- workCM = Count_Matrix[gt1rpin3,]
- cleanrs = rowSums(workCM)
- cleanN = length(cleanrs)
- meth = paste( "After removing",length(lo),"contigs with fewer than ",nscut," sample read counts >= 1 per million, there are",sep="")
- print(paste("Read",allN,"contigs. Removed",zN,"contigs with no reads.",meth,cleanN,"contigs"),quote=F)
- maint = paste('Filter >=1/million reads in >=',nscut,'samples')
- } else {
- useme = (nzrs > quantile(nzrs,filterquantile))
- workCM = nonzerod[useme,]
- lo = colSums(nonzerod[!useme,])
- cleanrs = rowSums(workCM)
- cleanN = length(cleanrs)
- meth = paste("After filtering at count quantile =",filterquantile,", there are",sep="")
- print(paste('Read',allN,"contigs. Removed",zN,"with no reads.",meth,cleanN,"contigs"),quote=F)
- maint = paste('Filter below',filterquantile,'quantile')
- }
- cumPlot(rawrs=rawrs,cleanrs=cleanrs,maint=maint,myTitle=myTitle)
- allgenes = rownames(workCM)
- reg = "^chr([0-9]+):([0-9]+)-([0-9]+)"
- genecards=" 0.8) # is ucsc style string
- {
- print("@@ using ucsc substitution for urls")
- contigurls = paste0(ucsc,"&position=chr",testreg[,2],":",testreg[,3],"-",testreg[,4],"\'>",allgenes," ")
- } else {
- print("@@ using genecards substitution for urls")
- contigurls = paste0(genecards,allgenes,"\'>",allgenes,"")
- }
- print.noquote("# urls")
- print.noquote(head(contigurls))
- print(paste("# Total low count contigs per sample = ",paste(lo,collapse=',')),quote=F)
- cmrowsums = rowSums(workCM)
- TName=unique(group)[1]
- CName=unique(group)[2]
- if (is.null(mydesign)) {
- if (length(subjects) == 0)
- {
- mydesign = model.matrix(~group)
- }
- else {
- subjf = factor(subjects)
- mydesign = model.matrix(~subjf+group) # we block on subject so make group last to simplify finding it
- }
- }
- print.noquote(paste('Using samples:',paste(colnames(workCM),collapse=',')))
- print.noquote('Using design matrix:')
- print.noquote(mydesign)
- if (doedgeR) {
- sink('edgeR.log')
- #### Setup DGEList object
- DGEList = DGEList(counts=workCM, group = group)
- DGEList = calcNormFactors(DGEList)
-
- DGEList = estimateGLMCommonDisp(DGEList,mydesign)
- comdisp = DGEList\$common.dispersion
- DGEList = estimateGLMTrendedDisp(DGEList,mydesign)
- if (edgeR_priordf > 0) {
- print.noquote(paste("prior.df =",edgeR_priordf))
- DGEList = estimateGLMTagwiseDisp(DGEList,mydesign,prior.df = edgeR_priordf)
- } else {
- DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
- }
- DGLM = glmFit(DGEList,design=mydesign)
- DE = glmLRT(DGLM,coef=ncol(DGLM\$design)) # always last one - subject is first if needed
- efflib = DGEList\$samples\$lib.size*DGEList\$samples\$norm.factors
- normData = (1e+06*DGEList\$counts/efflib)
- uoutput = cbind(
- Name=as.character(rownames(DGEList\$counts)),
- DE\$table,
- adj.p.value=p.adjust(DE\$table\$PValue, method=fdrtype),
- Dispersion=DGEList\$tagwise.dispersion,totreads=cmrowsums,normData,
- DGEList\$counts
- )
- soutput = uoutput[order(DE\$table\$PValue),] # sorted into p value order - for quick toptable
- goodness = gof(DGLM, pcutoff=fdrthresh)
- if (sum(goodness\$outlier) > 0) {
- print.noquote('GLM outliers:')
- print(paste(rownames(DGLM)[(goodness\$outlier)],collapse=','),quote=F)
- } else {
- print('No GLM fit outlier genes found\n')
- }
- z = limma::zscoreGamma(goodness\$gof.statistic, shape=goodness\$df/2, scale=2)
- pdf("edgeR_GoodnessofFit.pdf")
- qq = qqnorm(z, panel.first=grid(), main="tagwise dispersion")
- abline(0,1,lwd=3)
- points(qq\$x[goodness\$outlier],qq\$y[goodness\$outlier], pch=16, col="maroon")
- dev.off()
- estpriorn = getPriorN(DGEList)
- print(paste("Common Dispersion =",comdisp,"CV = ",sqrt(comdisp),"getPriorN = ",estpriorn),quote=F)
- efflib = DGEList\$samples\$lib.size*DGEList\$samples\$norm.factors
- normData = (1e+06*DGEList\$counts/efflib)
- uniqueg = unique(group)
- #### Plot MDS
- sample_colors = match(group,levels(group))
- sampleTypes = levels(factor(group))
- print.noquote(sampleTypes)
- pdf("edgeR_MDSplot.pdf")
- plotMDS.DGEList(DGEList,main=paste("edgeR MDS for",myTitle),cex=0.5,col=sample_colors,pch=sample_colors)
- legend(x="topleft", legend = sampleTypes,col=c(1:length(sampleTypes)), pch=19)
- grid(col="blue")
- dev.off()
- colnames(normData) = paste( colnames(normData),'N',sep="_")
- print(paste('Raw sample read totals',paste(colSums(nonzerod,na.rm=T),collapse=',')))
- nzd = data.frame(log(nonzerod + 1e-2,10))
- boxPlot(rawrs=nzd,cleanrs=log(normData,10),maint='TMM Normalisation',myTitle=myTitle,pdfname="edgeR_raw_norm_counts_box.pdf")
- write.table(soutput,file=out_edgeR, quote=FALSE, sep="\t",row.names=F)
- tt = cbind(
- Name=as.character(rownames(DGEList\$counts)),
- DE\$table,
- adj.p.value=p.adjust(DE\$table\$PValue, method=fdrtype),
- Dispersion=DGEList\$tagwise.dispersion,totreads=cmrowsums
- )
- print.noquote("# edgeR Top tags\n")
- tt = cbind(tt,URL=contigurls) # add to end so table isn't laid out strangely
- tt = tt[order(DE\$table\$PValue),]
- print.noquote(tt[1:50,])
- deTags = rownames(uoutput[uoutput\$adj.p.value < fdrthresh,])
- nsig = length(deTags)
- print(paste('#',nsig,'tags significant at adj p=',fdrthresh),quote=F)
- deColours = ifelse(deTags,'red','black')
- pdf("edgeR_BCV_vs_abundance.pdf")
- plotBCV(DGEList, cex=0.3, main="Biological CV vs abundance")
- dev.off()
- dg = DGEList[order(DE\$table\$PValue),]
- #normData = (1e+06 * dg\$counts/expandAsMatrix(dg\$samples\$lib.size, dim(dg)))
- efflib = dg\$samples\$lib.size*dg\$samples\$norm.factors
- normData = (1e+06*dg\$counts/efflib)
- outpdfname="edgeR_top_100_heatmap.pdf"
- hmap2(normData,nsamp=100,TName=TName,group=group,outpdfname=outpdfname,myTitle=paste('edgeR Heatmap',myTitle))
- outSmear = "edgeR_smearplot.pdf"
- outMain = paste("Smear Plot for ",TName,' Vs ',CName,' (FDR@',fdrthresh,' N = ',nsig,')',sep='')
- smearPlot(DGEList=DGEList,deTags=deTags, outSmear=outSmear, outMain = outMain)
- qqPlot(descr=paste(myTitle,'edgeR adj p QQ plot'),pvector=tt\$adj.p.value,outpdf='edgeR_qqplot.pdf')
- norm.factor = DGEList\$samples\$norm.factors
- topresults.edgeR = soutput[which(soutput\$adj.p.value < fdrthresh), ]
- edgeRcountsindex = which(allgenes %in% rownames(topresults.edgeR))
- edgeRcounts = rep(0, length(allgenes))
- edgeRcounts[edgeRcountsindex] = 1 # Create venn diagram of hits
- sink()
- } ### doedgeR
- if (doDESeq2 == T)
- {
- sink("DESeq2.log")
- # DESeq2
- require('DESeq2')
- library('RColorBrewer')
- pdata = data.frame(Name=colnames(workCM),Rx=group,row.names=colnames(workCM))
- deSEQds = DESeqDataSetFromMatrix(countData = workCM, colData = pdata, design = formula(~ Rx))
- #DESeq2 = DESeq(deSEQds,fitType='local',pAdjustMethod=fdrtype)
- #rDESeq = results(DESeq2)
- #newCountDataSet(workCM, group)
- deSeqDatsizefac = estimateSizeFactors(deSEQds)
- deSeqDatdisp = estimateDispersions(deSeqDatsizefac,fitType=DESeq_fitType)
- resDESeq = nbinomWaldTest(deSeqDatdisp, pAdjustMethod=fdrtype)
- rDESeq = as.data.frame(results(resDESeq))
- rDESeq = cbind(Contig=rownames(workCM),rDESeq,NReads=cmrowsums,URL=contigurls)
- srDESeq = rDESeq[order(rDESeq\$pvalue),]
- qqPlot(descr=paste(myTitle,'DESeq2 adj p qq plot'),pvector=rDESeq\$padj,outpdf='DESeq2_qqplot.pdf')
- cat("# DESeq top 50\n")
- print.noquote(srDESeq[1:50,])
- write.table(srDESeq,file=out_DESeq2, quote=FALSE, sep="\t",row.names=F)
- topresults.DESeq = rDESeq[which(rDESeq\$padj < fdrthresh), ]
- DESeqcountsindex = which(allgenes %in% rownames(topresults.DESeq))
- DESeqcounts = rep(0, length(allgenes))
- DESeqcounts[DESeqcountsindex] = 1
- pdf("DESeq2_dispersion_estimates.pdf")
- plotDispEsts(resDESeq)
- dev.off()
- ysmall = abs(min(rDESeq\$log2FoldChange))
- ybig = abs(max(rDESeq\$log2FoldChange))
- ylimit = min(4,ysmall,ybig)
- pdf("DESeq2_MA_plot.pdf")
- plotMA(resDESeq,main=paste(myTitle,"DESeq2 MA plot"),ylim=c(-ylimit,ylimit))
- dev.off()
- rlogres = rlogTransformation(resDESeq)
- sampledists = dist( t( assay(rlogres) ) )
- sdmat = as.matrix(sampledists)
- pdf("DESeq2_sample_distance_plot.pdf")
- heatmap.2(sdmat,trace="none",main=paste(myTitle,"DESeq2 sample distances"),
- col = colorRampPalette( rev(brewer.pal(9, "RdBu")) )(255))
- dev.off()
- sink()
- result = try( (ppca = plotPCA( varianceStabilizingTransformation(deSeqDatdisp,blind=T), intgroup=c("Rx","Name")) ) )
- if ("try-error" %in% class(result)) {
- print.noquote('DESeq2 plotPCA failed.')
- } else {
- pdf("DESeq2_PCA_plot.pdf")
- #### wtf - print? Seems needed to get this to work
- print(ppca)
- dev.off()
- }
- }
-
- if (doVoom == T) {
- sink('VOOM.log')
- if (doedgeR == F) {
- #### Setup DGEList object
- DGEList = DGEList(counts=workCM, group = group)
- DGEList = calcNormFactors(DGEList)
- DGEList = estimateGLMCommonDisp(DGEList,mydesign)
- DGEList = estimateGLMTrendedDisp(DGEList,mydesign)
- DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
- DGEList = estimateGLMTagwiseDisp(DGEList,mydesign)
- norm.factor = DGEList\$samples\$norm.factors
- }
- pdf("VOOM_mean_variance_plot.pdf")
- dat.voomed = voom(DGEList, mydesign, plot = TRUE, lib.size = colSums(workCM) * norm.factor)
- dev.off()
- # Use limma to fit data
- fit = lmFit(dat.voomed, mydesign)
- fit = eBayes(fit)
- rvoom = topTable(fit, coef = length(colnames(mydesign)), adj = fdrtype, n = Inf, sort="none")
- qqPlot(descr=paste(myTitle,'VOOM-limma adj p QQ plot'),pvector=rvoom\$adj.P.Val,outpdf='VOOM_qqplot.pdf')
- rownames(rvoom) = rownames(workCM)
- rvoom = cbind(rvoom,NReads=cmrowsums,URL=contigurls)
- srvoom = rvoom[order(rvoom\$P.Value),]
- cat("# VOOM top 50\n")
- print(srvoom[1:50,])
- write.table(srvoom,file=out_VOOM, quote=FALSE, sep="\t",row.names=F)
- # Use an FDR cutoff to find interesting samples for edgeR, DESeq and voom/limma
- topresults.voom = srvoom[which(rvoom\$adj.P.Val < fdrthresh), ]
- voomcountsindex = which(allgenes %in% topresults.voom\$ID)
- voomcounts = rep(0, length(allgenes))
- voomcounts[voomcountsindex] = 1
- sink()
- }
-
- if (doCamera) {
- doGSEA(y=DGEList,design=mydesign,histgmt=histgmt,bigmt=bigmt,ntest=20,myTitle=myTitle,
- outfname=paste(mt,"GSEA.xls",sep="_"),fdrthresh=fdrthresh,fdrtype=fdrtype)
- }
-
- if ((doDESeq2==T) || (doVoom==T) || (doedgeR==T)) {
- if ((doVoom==T) && (doDESeq2==T) && (doedgeR==T)) {
- vennmain = paste(mt,'Voom,edgeR and DESeq2 overlap at FDR=',fdrthresh)
- counts.dataframe = data.frame(edgeR = edgeRcounts, DESeq2 = DESeqcounts,
- VOOM_limma = voomcounts, row.names = allgenes)
- } else if ((doDESeq2==T) && (doedgeR==T)) {
- vennmain = paste(mt,'DESeq2 and edgeR overlap at FDR=',fdrthresh)
- counts.dataframe = data.frame(edgeR = edgeRcounts, DESeq2 = DESeqcounts, row.names = allgenes)
- } else if ((doVoom==T) && (doedgeR==T)) {
- vennmain = paste(mt,'Voom and edgeR overlap at FDR=',fdrthresh)
- counts.dataframe = data.frame(edgeR = edgeRcounts, VOOM_limma = voomcounts, row.names = allgenes)
- }
-
- if (nrow(counts.dataframe > 1)) {
- counts.venn = vennCounts(counts.dataframe)
- vennf = "Venn_significant_genes_overlap.pdf"
- pdf(vennf)
- vennDiagram(counts.venn,main=vennmain,col="maroon")
- dev.off()
- }
- } #### doDESeq2 or doVoom
-
-}
-#### Done
-
-###sink(stdout(),append=T,type="message")
-builtin_gmt=""
-history_gmt=""
-out_edgeR = F
-out_DESeq2 = F
-out_VOOM = "$out_VOOM"
-doDESeq2 = $DESeq2.doDESeq2 # make these T or F
-doVoom = $doVoom
-doCamera = F
-doedgeR = $edgeR.doedgeR
-edgeR_priordf = 0
-
-
-#if $doVoom == "T":
- out_VOOM = "$out_VOOM"
-#end if
-
-#if $DESeq2.doDESeq2 == "T":
- out_DESeq2 = "$out_DESeq2"
- DESeq_fitType = "$DESeq2.DESeq_fitType"
-#end if
-
-#if $edgeR.doedgeR == "T":
- out_edgeR = "$out_edgeR"
- edgeR_priordf = $edgeR.edgeR_priordf
-#end if
-
-if (sum(c(doedgeR,doVoom,doDESeq2)) == 0)
-{
-write("No methods chosen - nothing to do! Please try again after choosing one or more methods", stderr())
-quit(save="no",status=2)
-}
-
-Out_Dir = "$html_file.files_path"
-Input = "$input1"
-TreatmentName = "$treatment_name"
-TreatmentCols = "$Treat_cols"
-ControlName = "$control_name"
-ControlCols= "$Control_cols"
-org = "$input1.dbkey"
-if (org == "") { org = "hg19"}
-fdrtype = "$fdrtype"
-fdrthresh = $fdrthresh
-useNDF = $useNDF
-fQ = $fQ # non-differential centile cutoff
-myTitle = "$title"
-subjects = c($subjectids)
-nsubj = length(subjects)
-TCols = as.numeric(strsplit(TreatmentCols,",")[[1]])-1
-CCols = as.numeric(strsplit(ControlCols,",")[[1]])-1
-cat('Got TCols=')
-cat(TCols)
-cat('; CCols=')
-cat(CCols)
-cat('\n')
-useCols = c(TCols,CCols)
-if (file.exists(Out_Dir) == F) dir.create(Out_Dir)
-Count_Matrix = read.table(Input,header=T,row.names=1,sep='\t') #Load tab file assume header
-snames = colnames(Count_Matrix)
-nsamples = length(snames)
-if (nsubj > 0 & nsubj != nsamples) {
-options("show.error.messages"=T)
-mess = paste('Fatal error: Supplied subject id list',paste(subjects,collapse=','),
- 'has length',nsubj,'but there are',nsamples,'samples',paste(snames,collapse=','))
-write(mess, stderr())
-quit(save="no",status=4)
-}
-
-Count_Matrix = Count_Matrix[,useCols] ### reorder columns
-if (length(subjects) != 0) {subjects = subjects[useCols]}
-rn = rownames(Count_Matrix)
-islib = rn %in% c('librarySize','NotInBedRegions')
-LibSizes = Count_Matrix[subset(rn,islib),][1] # take first
-Count_Matrix = Count_Matrix[subset(rn,! islib),]
-group = c(rep(TreatmentName,length(TCols)), rep(ControlName,length(CCols)) ) #Build a group descriptor
-group = factor(group, levels=c(ControlName,TreatmentName))
-colnames(Count_Matrix) = paste(group,colnames(Count_Matrix),sep="_") #Relable columns
-results = edgeIt(Count_Matrix=Count_Matrix,group=group, out_edgeR=out_edgeR, out_VOOM=out_VOOM, out_DESeq2=out_DESeq2,
- fdrtype='BH',priordf=edgeR_priordf,fdrthresh=0.05,outputdir='.',
- myTitle=myTitle,useNDF=F,libSize=c(),filterquantile=fQ,subjects=c(),
- doDESeq2=doDESeq2,doVoom=doVoom,doCamera=doCamera,doedgeR=doedgeR,org=org,
- histgmt=history_gmt,bigmt=builtin_gmt,DESeq_fitType=DESeq_fitType)
-sessionInfo()
-]]>
-
-
-
-
-----
-
-**What it does**
-
-Allows short read sequence counts from controlled experiments to be analysed for differentially expressed genes.
-Optionally adds a term for subject if not all samples are independent or if some other factor needs to be blocked in the design.
-
-**Input**
-
-Requires a count matrix as a tabular file. These are best made using the companion HTSeq_ based counter Galaxy wrapper
-and your fave gene model to generate inputs. Each row is a genomic feature (gene or exon eg) and each column the
-non-negative integer count of reads from one sample overlapping the feature.
-The matrix must have a header row uniquely identifying the source samples, and unique row names in
-the first column. Typically the row names are gene symbols or probe ids for downstream use in GSEA and other methods.
-
-**Specifying comparisons**
-
-This is basically dumbed down for two factors - case vs control.
-
-More complex interfaces are possible but painful at present.
-Probably need to specify a phenotype file to do this better.
-Work in progress. Send code.
-
-If you have (eg) paired samples and wish to include a term in the GLM to account for some other factor (subject in the case of paired samples),
-put a comma separated list of indicators for every sample (whether modelled or not!) indicating (eg) the subject number or
-A list of integers, one for each subject or an empty string if samples are all independent.
-If not empty, there must be exactly as many integers in the supplied integer list as there are columns (samples) in the count matrix.
-Integers for samples that are not in the analysis *must* be present in the string as filler even if not used.
-
-So if you have 2 pairs out of 6 samples, you need to put in unique integers for the unpaired ones
-eg if you had 6 samples with the first two independent but the second and third pairs each being from independent subjects. you might use
-8,9,1,1,2,2
-as subject IDs to indicate two paired samples from the same subject in columns 3/4 and 5/6
-
-**Methods available**
-
-You can run 3 popular Bioconductor packages available for count data.
-
-edgeR - see edgeR_ for details
-
-VOOM/limma - see limma_VOOM_ for details
-
-DESeq2 - see DESeq2_ for details
-
-and optionally camera in edgeR which works better if MSigDB is installed.
-
-**Outputs**
-
-Some helpful plots and analysis results. Note that most of these are produced using R code
-suggested by the excellent documentation and vignettes for the Bioconductor
-packages invoked. The Tool Factory is used to automatically lay these out for you to enjoy.
-
-**Note on Voom**
-
-The voom from limma version 3.16.6 help in R includes this from the authors - but you should read the paper to interpret this method.
-
-This function is intended to process RNA-Seq or ChIP-Seq data prior to linear modelling in limma.
-
-voom is an acronym for mean-variance modelling at the observational level.
-The key concern is to estimate the mean-variance relationship in the data, then use this to compute appropriate weights for each observation.
-Count data almost show non-trivial mean-variance relationships. Raw counts show increasing variance with increasing count size, while log-counts typically show a decreasing mean-variance trend.
-This function estimates the mean-variance trend for log-counts, then assigns a weight to each observation based on its predicted variance.
-The weights are then used in the linear modelling process to adjust for heteroscedasticity.
-
-In an experiment, a count value is observed for each tag in each sample. A tag-wise mean-variance trend is computed using lowess.
-The tag-wise mean is the mean log2 count with an offset of 0.5, across samples for a given tag.
-The tag-wise variance is the quarter-root-variance of normalized log2 counts per million values with an offset of 0.5, across samples for a given tag.
-Tags with zero counts across all samples are not included in the lowess fit. Optional normalization is performed using normalizeBetweenArrays.
-Using fitted values of log2 counts from a linear model fit by lmFit, variances from the mean-variance trend were interpolated for each observation.
-This was carried out by approxfun. Inverse variance weights can be used to correct for mean-variance trend in the count data.
-
-
-Author(s)
-
-Charity Law and Gordon Smyth
-
-References
-
-Law, CW (2013). Precision weights for gene expression analysis. PhD Thesis. University of Melbourne, Australia.
-
-Law, CW, Chen, Y, Shi, W, Smyth, GK (2013). Voom! Precision weights unlock linear model analysis tools for RNA-seq read counts.
-Technical Report 1 May 2013, Bioinformatics Division, Walter and Eliza Hall Institute of Medical Reseach, Melbourne, Australia.
-http://www.statsci.org/smyth/pubs/VoomPreprint.pdf
-
-See Also
-
-A voom case study is given in the edgeR User's Guide.
-
-vooma is a similar function but for microarrays instead of RNA-seq.
-
-
-***old rant on changes to Bioconductor package variable names between versions***
-
-The edgeR authors made a small cosmetic change in the name of one important variable (from p.value to PValue)
-breaking this and all other code that assumed the old name for this variable,
-between edgeR2.4.4 and 2.4.6 (the version for R 2.14 as at the time of writing).
-This means that all code using edgeR is sensitive to the version. I think this was a very unwise thing
-to do because it wasted hours of my time to track down and will similarly cost other edgeR users dearly
-when their old scripts break. This tool currently now works with 2.4.6.
-
-**Note on prior.N**
-
-http://seqanswers.com/forums/showthread.php?t=5591 says:
-
-*prior.n*
-
-The value for prior.n determines the amount of smoothing of tagwise dispersions towards the common dispersion.
-You can think of it as like a "weight" for the common value. (It is actually the weight for the common likelihood
-in the weighted likelihood equation). The larger the value for prior.n, the more smoothing, i.e. the closer your
-tagwise dispersion estimates will be to the common dispersion. If you use a prior.n of 1, then that gives the
-common likelihood the weight of one observation.
-
-In answer to your question, it is a good thing to squeeze the tagwise dispersions towards a common value,
-or else you will be using very unreliable estimates of the dispersion. I would not recommend using the value that
-you obtained from estimateSmoothing()---this is far too small and would result in virtually no moderation
-(squeezing) of the tagwise dispersions. How many samples do you have in your experiment?
-What is the experimental design? If you have few samples (less than 6) then I would suggest a prior.n of at least 10.
-If you have more samples, then the tagwise dispersion estimates will be more reliable,
-so you could consider using a smaller prior.n, although I would hesitate to use a prior.n less than 5.
-
-
-From Bioconductor Digest, Vol 118, Issue 5, Gordon writes:
-
-Dear Dorota,
-
-The important settings are prior.df and trend.
-
-prior.n and prior.df are related through prior.df = prior.n * residual.df,
-and your experiment has residual.df = 36 - 12 = 24. So the old setting of
-prior.n=10 is equivalent for your data to prior.df = 240, a very large
-value. Going the other way, the new setting of prior.df=10 is equivalent
-to prior.n=10/24.
-
-To recover old results with the current software you would use
-
- estimateTagwiseDisp(object, prior.df=240, trend="none")
-
-To get the new default from old software you would use
-
- estimateTagwiseDisp(object, prior.n=10/24, trend=TRUE)
-
-Actually the old trend method is equivalent to trend="loess" in the new
-software. You should use plotBCV(object) to see whether a trend is
-required.
-
-Note you could also use
-
- prior.n = getPriorN(object, prior.df=10)
-
-to map between prior.df and prior.n.
-
-----
-
-**Attributions**
-
-edgeR - edgeR_
-
-VOOM/limma - limma_VOOM_
-
-DESeq2 - DESeq2_ for details
-
-See above for Bioconductor package documentation for packages exposed in Galaxy by this tool and app store package.
-
-Galaxy_ (that's what you are using right now!) for gluing everything together
-
-Otherwise, all code and documentation comprising this tool was written by Ross Lazarus and is
-licensed to you under the LGPL_ like other rgenetics artefacts
-
-.. _LGPL: http://www.gnu.org/copyleft/lesser.html
-.. _HTSeq: http://www-huber.embl.de/users/anders/HTSeq/doc/index.html
-.. _edgeR: http://www.bioconductor.org/packages/release/bioc/html/edgeR.html
-.. _DESeq2: http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html
-.. _limma_VOOM: http://www.bioconductor.org/packages/release/bioc/html/limma.html
-.. _Galaxy: http://getgalaxy.org
-
-
-
-
-
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Rscript log
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-## Toolfactory generated command line = Rscript - None /data/home/rlazarus/galaxy-central/database/files/000/dataset_2.dat
-
-Loading required package: gtools
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-Loading required package: gdata
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-gdata: read.xls support for 'XLS' (Excel 97-2004) files ENABLED.
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-gdata: read.xls support for 'XLSX' (Excel 2007+) files ENABLED.
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-Welcome to Bioconductor
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-locfit 1.5-9.1 2013-03-22
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-Loading required package: limma
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-The following object(s) are masked from ‘package:DESeq’:
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-# got TCols=2 3 4 8; CCols=1 5 6 7
-
-[1] # Quantiles for non-zero row counts:
-
- 0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%
-
- 1.0 1.0 2.0 3.0 4.0 8.0 13.0 24.0 86.6 753.0 2325567.0
-
-[1] Read 3242 contigs. Removed 1494 with no reads. After filtering at count quantile =0.3, there are 1141 contigs
-
-[1] # Total low count contigs per sample = 145,111,155,120,170,67,203,86
-
-Calculating library sizes from column totals.
-
-[1] Using samples: case_X11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam,case_X11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam,case_X11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam,case_X11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam,control_X11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam,control_X11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam,control_X11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam,control_X11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam
-
-[1] Using design matrix:
-
- (Intercept) groupcase
-
-1 1 1
-
-2 1 1
-
-3 1 1
-
-4 1 1
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-5 1 0
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-6 1 0
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-7 1 0
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-8 1 0
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-attr(,"assign")
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-[1] 0 1
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-attr(,"contrasts")
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-attr(,"contrasts")$group
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-[1] contr.treatment
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-[1] "No GLM fit outlier genes found\n"
-
-[1] Common Dispersion = 0.24088423096811 CV = 0.490799583300669 getPriorN = 3.33333333333333
-
-[1] "Raw sample read totals 1440960,1341813,2888924,1428365,2443751,1644652,1682104,1806045"
-
-[1] raw contig counts by sample:
-
- case_X11706He_AGTTCC case_X11699He_GGCTAC case_X11698He_TAGCTT case_X11700He_CTTGTA control_X11706Liv_CA control_X11700Liv_AT control_X11698Liv_AC control_X11699Liv_AT
-
- Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043 Min. :0.0043
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- 1st Qu.:0.0043 1st Qu.:0.0043 1st Qu.:0.0043 1st Qu.:0.0043 1st Qu.:0.3032 1st Qu.:0.0043 1st Qu.:0.3032 1st Qu.:0.0043
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- Median :0.4786 Median :0.4786 Median :0.4786 Median :0.4786 Median :0.7789 Median :0.6031 Median :0.6998 Median :0.6031
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- Mean :0.9210 Mean :0.9428 Mean :1.0205 Mean :0.9753 Mean :1.0519 Mean :1.0343 Mean :0.9855 Mean :0.9966
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- 3rd Qu.:1.5770 3rd Qu.:1.5855 3rd Qu.:1.7161 3rd Qu.:1.6022 3rd Qu.:1.5410 3rd Qu.:1.6335 3rd Qu.:1.4473 3rd Qu.:1.5534
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- NA's :902 NA's :957 NA's :821 NA's :950 NA's :650 NA's :969 NA's :664 NA's :886
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-[1] normalised contig counts by sample:
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- case_X11706He_AGTTCC case_X11699He_GGCTAC case_X11698He_TAGCTT case_X11700He_CTTGTA control_X11706Liv_CA control_X11700Liv_AT control_X11698Liv_AC control_X11699Liv_AT
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- Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf Min. :-Inf
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- 1st Qu.:-Inf 1st Qu.:-Inf 1st Qu.:-Inf 1st Qu.:-Inf 1st Qu.: 0 1st Qu.:-Inf 1st Qu.: 0 1st Qu.:-Inf
-
- Median : 0 Median : 0 Median : 0 Median : 0 Median : 0 Median : 0 Median : 0 Median : 0
-
- Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf Mean :-Inf
-
- 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1 3rd Qu.: 1
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- Max. : 5 Max. : 5 Max. : 6 Max. : 5 Max. : 6 Max. : 6 Max. : 6 Max. : 5
-
-[1] Using ncol rawrs= 8
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-[1] # writing output
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-[1] # urls
-
- 0610005C13Rik 0610007N19Rik 0610008F07Rik 0610009L18Rik 0610012G03Rik 0610031O16Rik# Top tags
-
- Name logFC logCPM LR PValue adj.p.value Dispersion totreads case_X11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam control_X11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam
-
-Mir122a Mir122a -10.661348 12.537949 445.91203 5.594743e-99 6.383602e-96 0.10205510 90428 6.644669 2.864648e+00 2.012369e+01 4.756523e+00 2.084166e+04 1.681895e+04
-
-Mir192 Mir192 -7.109019 17.247415 366.13166 1.301558e-81 7.425390e-79 0.07765487 2325567 1779.663879 1.294412e+03 4.493546e+03 1.933526e+03 4.635990e+05 3.403123e+05
-
-Mir208b Mir208b 13.423720 9.822338 355.41782 2.801296e-79 1.065426e-76 0.12444059 14756 1245.907022 5.701390e+02 4.930344e+03 8.819024e+02 7.453220e-01 0.000000e+00
-
-Mir208a Mir208a 11.977586 8.388290 348.81540 7.675451e-78 2.189422e-75 0.09936798 4638 433.789590 7.125278e+02 1.006599e+03 6.497485e+02 0.000000e+00 0.000000e+00
-
-Mir499 Mir499 14.488216 8.612770 291.12794 2.823507e-65 6.443244e-63 0.13481620 6527 608.439028 5.066577e+02 2.521609e+03 2.703574e+02 0.000000e+00 0.000000e+00
-
-Mir149 Mir149 6.869731 8.785665 253.01986 5.702930e-57 1.084507e-54 0.09834684 6164 774.657675 4.595714e+02 1.710514e+03 7.663947e+02 1.750400e+01 6.246465e+00
-
-Mir490 Mir490 8.453930 6.909596 251.05610 1.528281e-56 2.491098e-54 0.09745005 1741 209.881557 2.177498e+02 5.205387e+02 1.957941e+02 1.038505e+00 5.537224e-01
-
-Mir802 Mir802 -12.499678 6.629391 237.56161 1.337812e-53 1.908055e-51 0.10939981 1514 0.000000 0.000000e+00 0.000000e+00 0.000000e+00 3.056548e+02 1.641034e+02
-
-Mir204 Mir204 7.371179 7.558996 237.12302 1.667365e-53 2.113848e-51 0.10292005 2601 425.578854 3.264164e+02 6.462477e+02 3.754819e+02 3.040281e+00 6.923364e-01
-
-Mir1948 Mir1948 -7.583326 7.293456 204.79641 1.875897e-46 2.140399e-44 0.11833999 2404 1.216112 6.923364e-01 1.661167e+00 1.636942e+00 6.476848e+02 3.852783e+02
-
-Mir3073 Mir3073 -11.748556 5.881462 200.03350 2.053625e-45 2.130170e-43 0.11068562 904 0.000000 0.000000e+00 0.000000e+00 0.000000e+00 2.073471e+02 7.546467e+01
-
-Mir194-2 Mir194-2 -5.439827 7.860048 165.57239 6.859199e-38 6.521955e-36 0.10671020 3570 10.520726 6.138532e+00 1.490644e+01 9.513045e+00 9.214105e+02 6.003547e+02
-
-Mir10b Mir10b 5.032898 13.880770 160.06580 1.094640e-36 9.607570e-35 0.10795434 197340 25838.822630 3.216361e+04 3.631730e+04 3.446522e+04 1.825385e+03 3.738617e+02
-
-Mir101b Mir101b -3.925287 11.936090 120.62427 4.618143e-28 3.763787e-26 0.09663075 59019 219.816815 3.012250e+02 8.119232e+02 4.270695e+02 1.014507e+04 7.747970e+03
-
-Mir182 Mir182 -5.244384 8.942708 118.92815 1.085926e-27 8.260276e-26 0.14993443 7189 16.962242 1.439678e+01 2.209871e+01 3.130352e+01 9.840056e+02 6.154406e+02
-
-Mir200b Mir200b -6.725348 5.765187 115.73189 5.440989e-27 3.880105e-25 0.16712490 888 2.432225 0.000000e+00 1.661167e+00 0.000000e+00 3.696797e+02 9.750871e+01
-
-Mir181c Mir181c 3.611867 10.569815 107.82011 2.943153e-25 1.975375e-23 0.09385270 23605 2420.852087 1.892879e+03 4.093093e+03 1.902590e+03 2.320365e+02 2.727878e+02
-
-Mir181d Mir181d 3.489976 7.232064 102.18661 5.053019e-24 3.203053e-22 0.08738498 2139 310.053946 2.021522e+02 5.398233e+02 2.956660e+02 3.648337e+01 1.453906e+01
-
-Mir21 Mir21 -3.077771 13.881500 91.37324 1.189745e-21 7.144733e-20 0.08494272 229120 3207.212585 2.190826e+03 4.348911e+03 2.010566e+03 2.715400e+04 3.322794e+04
-
-Mir199b Mir199b 5.411476 4.695869 86.70372 1.260596e-20 7.191701e-19 0.15656183 370 43.403268 4.481024e+01 9.924938e+01 4.925255e+01 1.384673e+00 5.537224e-01
-
-Mir193 Mir193 -5.360157 4.775477 84.66127 3.541205e-20 1.924055e-18 0.15546497 421 1.490644 1.189131e+00 2.800640e+00 6.940516e-01 1.015454e+02 3.496299e+01
-
-Mir23a Mir23a 3.003071 9.467420 82.28684 1.177029e-19 6.104501e-18 0.08920345 10118 1149.889322 1.127958e+03 2.471518e+03 1.096325e+03 1.505832e+02 1.268024e+02
-
-Mir195 Mir195 3.060546 8.152797 81.39727 1.846126e-19 9.158392e-18 0.09133016 3962 429.134881 2.831909e+02 9.227086e+02 4.708957e+02 1.106253e+02 7.773378e+01
-
-Ahsg Ahsg -10.101343 6.638589 79.82133 4.098447e-19 1.923759e-17 0.42092199 1524 0.000000 5.537224e-01 0.000000e+00 0.000000e+00 3.484153e+02 1.260288e+01
-
-Mir148a Mir148a -2.789375 16.047169 79.76589 4.215073e-19 1.923759e-17 0.08196054 1002397 15925.598251 8.528200e+03 2.207082e+04 1.059020e+04 1.927239e+05 1.054456e+05
-
-Dnm3os Dnm3os 3.189443 6.618834 79.19614 5.623979e-19 2.468062e-17 0.09496531 1401 134.000827 8.716715e+01 3.652078e+02 1.825316e+02 3.710848e+01 2.498586e+01
-
-Mir27a Mir27a 2.921772 10.581277 77.26988 1.491231e-18 6.301832e-17 0.09125059 21886 2383.612353 2.512174e+03 5.321988e+03 2.361690e+03 3.285136e+02 3.477377e+02
-
-Mir429 Mir429 -5.341934 4.951103 76.38758 2.331128e-18 9.499346e-17 0.18324117 499 1.783696 7.001600e-01 2.082155e+00 1.824168e+00 9.173458e+01 4.540524e+01
-
-Mir214 Mir214 3.125906 6.202347 74.28213 6.771387e-18 2.664191e-16 0.09532762 1048 110.058161 5.642542e+01 1.982326e+02 9.371492e+01 3.353949e+01 1.545870e+01
-
-Mir200a Mir200a -7.592263 4.059943 73.71426 9.028450e-18 3.433821e-16 0.22417820 264 0.000000 0.000000e+00 5.945653e-01 0.000000e+00 9.022671e+01 3.222698e+01
-
-Mir194-1 Mir194-1 -3.970219 5.393899 73.22380 1.157517e-17 4.260408e-16 0.13095886 635 3.567392 9.102080e+00 5.552413e+00 3.648337e+00 7.615701e+01 8.859559e+01
-
-Mir378 Mir378 2.954320 8.053368 73.09647 1.234655e-17 4.402315e-16 0.09566655 4075 425.697272 3.921392e+02 1.155915e+03 1.883155e+02 7.641369e+01 3.683119e+01
-
-Mir322 Mir322 3.058569 8.948242 72.83721 1.407969e-17 4.868160e-16 0.10365695 7074 1012.892580 6.718588e+02 1.784708e+03 8.550716e+02 1.587027e+02 7.892635e+01
-
-Mir215 Mir215 2.908934 6.381924 70.31105 5.065317e-17 1.699861e-15 0.09002036 1182 123.075020 1.610368e+02 2.727623e+02 1.222193e+02 1.938542e+01 1.716540e+01
-
-Cyp3a25 Cyp3a25 -9.778602 3.913257 70.02642 5.851533e-17 1.907600e-15 0.26445237 226 0.000000 0.000000e+00 0.000000e+00 0.000000e+00 5.664447e+01 1.783696e+01
-
-Mir183 Mir183 -4.214462 5.247929 66.31101 3.851010e-16 1.220556e-14 0.15955164 563 8.401920 1.388103e+00 2.432225e+00 2.423177e+00 8.638070e+01 2.905572e+01
-
-Mir181a-2 Mir181a-2 2.837713 7.573798 65.52900 5.726500e-16 1.765929e-14 0.09834030 2817 288.826664 1.377749e+02 6.395494e+02 1.821098e+02 5.813511e+01 4.102501e+01
-
-Mir155 Mir155 3.734310 4.975364 65.07600 7.206449e-16 2.163831e-14 0.13295455 463 33.966543 5.888044e+01 1.141565e+02 5.251200e+01 9.716723e+00 1.824168e+00
-
-Snord91a Snord91a -2.818342 6.592251 64.29345 1.072014e-15 3.136329e-14 0.09422446 1437 13.846728 1.605795e+01 3.314807e+01 1.863305e+01 2.158272e+02 1.792410e+02
-
-Mir125b-2 Mir125b-2 2.852233 8.081093 64.20822 1.119409e-15 3.193115e-14 0.10276578 3837 315.520541 4.404853e+02 7.634219e+02 4.852109e+02 1.082721e+02 9.060036e+01
-
-Serpina4-ps1 Serpina4-ps1 -10.090564 4.224051 64.02094 1.231040e-15 3.425894e-14 0.34406452 295 0.000000 0.000000e+00 0.000000e+00 0.000000e+00 1.080717e+02 1.129674e+01
-
-Mir133b Mir133b 9.293392 3.404704 63.59576 1.527577e-15 4.149919e-14 0.26404392 159 17.719118 1.064012e+01 5.738979e+01 1.426957e+01 0.000000e+00 0.000000e+00
-
-Gm10069 Gm10069 -7.475459 6.400326 63.15445 1.911172e-15 5.071271e-14 0.41541432 1309 1.189131 1.400320e+00 6.940516e-01 6.080561e-01 1.914310e+02 6.644669e+00
-
-Mir871 Mir871 -5.633588 4.283233 62.67513 2.437746e-15 6.321517e-14 0.21907826 290 1.227706 7.453220e-01 5.945653e-01 0.000000e+00 5.691223e+01 4.925255e+01
-
-Mir184 Mir184 5.002968 4.123691 61.97642 3.475940e-15 8.813439e-14 0.19289992 247 33.443087 1.419290e+01 4.983502e+01 2.168948e+01 2.981288e+00 0.000000e+00
-
-Mir132 Mir132 2.702863 5.866134 58.80773 1.738573e-14 4.312416e-13 0.09148478 857 82.695634 4.327103e+01 1.821747e+02 6.097608e+01 2.832224e+01 1.308044e+01
-
-Snord104 Snord104 -2.492063 11.108871 58.55547 1.976394e-14 4.798012e-13 0.09093023 33458 614.929745 4.378004e+02 8.629974e+02 5.144081e+02 3.826761e+03 4.181256e+03
-
-Mir3074-2 Mir3074-2 2.635505 7.871042 57.72938 3.007773e-14 7.149726e-13 0.09900198 3470 450.903031 3.206519e+02 8.354691e+02 1.716994e+02 8.970303e+01 5.197290e+01
-
-Mir24-2 Mir24-2 2.635505 7.871042 57.68174 3.081509e-14 7.175515e-13 0.09908656 3470 479.987359 2.746892e+02 9.620198e+02 3.442496e+02 9.850509e+01 4.396336e+01
-
-5430416N02Rik 5430416N02Rik -3.267228 5.202367 56.75137 4.945455e-14 1.128553e-12 0.12456687 564 6.080561 1.730841e+00 1.273562e+01 4.910826e+00 1.453378e+02 5.886197e+01
-
- control_X11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam case_X11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam control_X11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam
-
-Mir122a 7.242557e+03 8.468313e+03 12 7 27 8 29767
-
-Mir192 3.835916e+05 1.822922e+05 3214 3163 6029 3252 662133
-
-Mir208b 0.000000e+00 0.000000e+00 2049 1647 8904 2155 1
-
-Mir208a 0.000000e+00 5.537224e-01 1060 956 1693 928 0
-
-Mir499 0.000000e+00 0.000000e+00 869 730 4147 781 0
-
-Mir149 4.864449e+00 5.538691e+00 1399 1123 2295 1289 25
-
-Mir490 0.000000e+00 7.453220e-01 353 311 750 322 3
-
-Mir802 1.557723e+02 2.092870e+02 0 0 0 0 552
-
-Mir204 5.537224e-01 3.683119e+00 571 549 923 541 5
-
-Mir1948 1.813414e+02 4.282299e+02 2 2 3 4 869
-
-Mir3073 7.253764e+01 8.757639e+01 0 0 0 0 341
-
-Mir194-2 2.669366e+02 3.046280e+02 19 15 20 16 1316
-
-Mir10b 6.583760e+02 7.272114e+02 34668 54096 51870 49658 3002
-
-Mir101b 1.128042e+04 6.628420e+03 635 544 1984 573 17063
-
-Mir182 2.366022e+03 6.536603e+02 49 26 54 42 1655
-
-Mir200b 4.621056e+01 1.075780e+02 4 0 3 0 496
-
-Mir181c 2.283131e+02 2.989683e+02 3488 3113 11824 3436 567
-
-Mir181d 2.547123e+01 1.555095e+01 416 340 771 426 60
-
-Mir21 2.570722e+04 3.537908e+04 4621 3603 12563 3631 66353
-
-Mir199b 0.000000e+00 2.981288e+00 73 64 143 81 4
-
-Mir193 3.377707e+01 3.396654e+01 2 2 4 1 167
-
-Mir23a 8.921333e+01 2.437203e+02 1934 1611 3561 1803 435
-
-Mir195 4.560421e+01 4.154019e+01 775 692 1238 792 158
-
-Ahsg 6.100714e+02 2.432225e+01 0 1 0 0 586
-
-Mir148a 1.795497e+05 1.342747e+05 26191 24636 39859 25878 258578
-
-Dnm3os 1.216112e+01 1.384673e+01 242 213 490 307 53
-
-Mir27a 1.636942e+02 5.664447e+02 4009 3588 7668 3884 949
-
-Mir429 1.677865e+01 7.527752e+01 3 1 3 3 265
-
-Mir214 1.190272e+01 2.012750e+01 181 163 358 229 45
-
-Mir200a 1.142355e+01 2.602495e+01 0 0 1 0 130
-
-Mir194-1 3.314807e+01 1.050904e+02 6 13 8 6 220
-
-Mir378 9.167460e+01 6.302392e+01 608 565 1901 544 138
-
-Mir322 5.038874e+01 9.166874e+01 1359 1130 2549 1232 261
-
-Mir215 1.145859e+01 2.683159e+01 207 230 393 201 56
-
-Cyp3a25 6.511488e+01 1.873939e+01 0 0 0 0 76
-
-Mir183 1.349033e+02 7.729349e+01 12 2 4 7 156
-
-Mir181a-2 8.051840e+01 5.691223e+01 475 398 1155 445 78
-
-Mir155 2.769346e+00 4.983502e+00 83 79 192 75 14
-
-Snord91a 2.484705e+02 1.732960e+02 40 29 81 25 363
-
-Mir125b-2 2.077009e+01 7.364508e+01 771 591 1284 693 156
-
-Serpina4-ps1 8.191872e+01 9.716723e+00 0 0 0 0 145
-
-Mir133b 0.000000e+00 0.000000e+00 32 26 77 24 0
-
-Gm10069 2.868741e+02 2.757691e+01 2 2 1 1 553
-
-Mir871 1.003888e+01 5.149619e+01 3 1 1 0 82
-
-Mir184 1.400320e+00 1.388103e+00 55 41 90 53 4
-
-Mir132 2.100480e+01 1.943345e+01 136 125 329 149 38
-
-Snord104 4.430701e+03 4.212863e+03 886 720 2493 929 9351
-
-Mir3074-2 4.844593e+01 8.323914e+01 644 462 1374 496 162
-
-Mir24-2 3.599196e+01 5.729296e+01 644 462 1374 496 162
-
-5430416N02Rik 5.531264e+01 9.786128e+01 10 5 23 12 195
-
- control_X11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam ntotreads URL
-
-Mir122a 24233 11911 24463 90428 Mir122a
-
-Mir192 490327 630849 526600 2325567 Mir192
-
-Mir208b 0 0 0 14756 Mir208b
-
-Mir208a 0 0 1 4638 Mir208a
-
-Mir499 0 0 0 6527 Mir499
-
-Mir149 9 8 16 6164 Mir149
-
-Mir490 1 0 1 1741 Mir490
-
-Mir802 401 209 352 1514 Mir802
-
-Mir204 2 1 9 2601 Mir204
-
-Mir1948 648 259 617 2404 Mir1948
-
-Mir3073 218 131 214 904 Mir3073
-
-Mir194-2 865 439 880 3570 Mir194-2
-
-Mir10b 1080 1189 1777 197340 Mir10b
-
-Mir101b 11066 16253 10901 59019 Mir101b
-
-Mir182 879 3409 1075 7189 Mir182
-
-Mir200b 164 66 155 888 Mir200b
-
-Mir181c 366 384 427 23605 Mir181c
-
-Mir181d 42 46 38 2139 Mir181d
-
-Mir21 44582 43237 50530 229120 Mir21
-
-Mir199b 1 0 4 370 Mir199b
-
-Mir193 101 61 83 421 Mir193
-
-Mir23a 229 218 327 10118 Mir23a
-
-Mir195 112 75 120 3962 Mir195
-
-Ahsg 18 879 40 1524 Ahsg
-
-Mir148a 177349 256441 193465 1002397 Mir148a
-
-Dnm3os 36 20 40 1401 Dnm3os
-
-Mir27a 628 400 760 21886 Mir27a
-
-Mir429 82 41 101 499 Mir429
-
-Mir214 26 17 29 1048 Mir214
-
-Mir200a 53 33 47 264 Mir200a
-
-Mir194-1 160 81 141 635 Mir194-1
-
-Mir378 90 123 106 4075 Mir378
-
-Mir322 228 91 224 7074 Mir322
-
-Mir215 31 28 36 1182 Mir215
-
-Cyp3a25 30 93 27 226 Cyp3a25
-
-Mir183 71 181 130 563 Mir183
-
-Mir181a-2 69 115 82 2817 Mir181a-2
-
-Mir155 3 8 9 463 Mir155
-
-Snord91a 256 358 285 1437 Snord91a
-
-Mir125b-2 149 60 133 3837 Mir125b-2
-
-Serpina4-ps1 19 117 14 295 Serpina4-ps1
-
-Mir133b 0 0 0 159 Mir133b
-
-Gm10069 12 701 37 1309 Gm10069
-
-Mir871 81 29 93 290 Mir871
-
-Mir184 0 2 2 247 Mir184
-
-Mir132 22 30 28 857 Mir132
-
-Snord104 5610 7452 6017 33458 Snord104
-
-Mir3074-2 127 65 140 3470 Mir3074-2
-
-Mir24-2 127 65 140 3470 Mir24-2
-
-5430416N02Rik 99 79 141 564 5430416N02Rik
-
-[1] # 445 tags significant at adj p= 0.05
-
-[1] # deTags
-
-[1] "0610005C13Rik" "0610007N19Rik" "0610008F07Rik" "0610012G03Rik" "0610031O16Rik" "1110038B12Rik"
-
-# DESeq top 50
-
- id baseMean baseMeanA baseMeanB foldChange log2FoldChange pval padj
-
-536 Mir122a 10112.31117 2.021162e+04 1.300527e+01 6.434550e-04 -10.601873 5.488369e-57 6.262229e-54
-
-645 Mir208a 616.76981 2.430915e-01 1.233297e+03 5.073385e+03 12.308733 6.046036e-53 3.449263e-50
-
-600 Mir192 271352.97636 5.385927e+05 4.113233e+03 7.637001e-03 -7.032778 1.311798e-38 4.989204e-36
-
-568 Mir149 810.35429 1.224267e+01 1.608466e+03 1.313819e+02 7.037623 7.073079e-37 2.017596e-34
-
-791 Mir490 220.99790 9.450198e-01 4.410508e+02 4.667107e+02 8.866385 1.354865e-36 3.091803e-34
-
-642 Mir204 347.57397 3.737736e+00 6.914102e+02 1.849810e+02 7.531234 8.058436e-36 1.532446e-33
-
-844 Mir802 166.83414 3.336683e+02 0.000000e+00 0.000000e+00 -Inf 3.255469e-35 5.306414e-33
-
-698 Mir3073 98.93199 1.978640e+02 0.000000e+00 0.000000e+00 -Inf 1.111351e-28 1.585065e-26
-
-646 Mir208b 1649.77924 1.445675e-01 3.299414e+03 2.282265e+04 14.478178 7.505934e-28 9.515857e-26
-
-614 Mir1948 263.89527 5.246983e+02 3.092210e+00 5.893310e-03 -7.406706 1.534188e-26 1.750509e-24
-
-608 Mir194-2 391.65678 7.637703e+02 1.954329e+01 2.558791e-02 -5.288394 1.622682e-24 1.683163e-22
-
-796 Mir499 712.45950 0.000000e+00 1.424919e+03 Inf Inf 2.577318e-19 2.450600e-17
-
-585 Mir181c 2765.96510 3.955399e+02 5.136390e+03 1.298577e+01 3.698860 1.942959e-17 1.705320e-15
-
-631 Mir199b 47.84725 1.818862e+00 9.387565e+01 5.161231e+01 5.689643 4.012622e-15 3.270287e-13
-
-530 Mir10b 27820.40551 1.501200e+03 5.413961e+04 3.606421e+01 5.172496 3.069912e-14 2.335180e-12
-
-586 Mir181d 275.22797 4.254569e+01 5.079103e+02 1.193800e+01 3.577489 5.204519e-14 3.711473e-12
-
-602 Mir193 45.70861 8.913819e+01 2.279021e+00 2.556728e-02 -5.289558 1.657854e-13 1.112713e-11
-
-637 Mir200a 27.09009 5.402561e+01 1.545578e-01 2.860824e-03 -8.449354 2.466964e-13 1.563781e-11
-
-722 Mir322 899.53469 1.797868e+02 1.619283e+03 9.006682e+00 3.170996 1.359804e-12 8.165978e-11
-
-756 Mir378 483.21548 1.056050e+02 8.608260e+02 8.151374e+00 3.027043 2.046396e-12 1.160965e-10
-
-523 Mir101b 6846.19683 1.280838e+04 8.840090e+02 6.901800e-02 -3.856884 2.136745e-12 1.160965e-10
-
-552 Mir133b 19.46050 0.000000e+00 3.892101e+01 Inf Inf 2.388227e-12 1.238621e-10
-
-663 Mir23a 1289.18043 2.671574e+02 2.311203e+03 8.651093e+00 3.112882 3.093049e-12 1.534421e-10
-
-671 Mir27a 2788.72629 6.066392e+02 4.970813e+03 8.194019e+00 3.034571 5.970859e-12 2.838646e-10
-
-616 Mir195 519.86200 1.038507e+02 9.358733e+02 9.011721e+00 3.171803 6.245320e-12 2.850364e-10
-
-607 Mir194-1 71.10636 1.325374e+02 9.675354e+00 7.300095e-02 -3.775941 1.405195e-11 6.166645e-10
-
-344 Dnm3os 179.61643 3.285433e+01 3.263785e+02 9.934110e+00 3.312391 1.503324e-11 6.352936e-10
-
-590 Mir184 32.23796 1.645700e+00 6.283021e+01 3.817841e+01 5.254685 1.644760e-11 6.702396e-10
-
-582 Mir181a-2 347.82506 8.313904e+01 6.125111e+02 7.367310e+00 2.881138 2.735424e-11 1.076248e-09
-
-541 Mir125b-2 493.08516 1.122867e+02 8.738836e+02 7.782608e+00 2.960254 5.662328e-11 2.153572e-09
-
-573 Mir155 57.66182 7.341434e+00 1.079822e+02 1.470860e+01 3.878588 6.173765e-11 2.272344e-09
-
-464 Gm5441 20.24317 2.430915e-01 4.024325e+01 1.655478e+02 7.371104 6.503611e-11 2.318944e-09
-
-571 Mir153 19.90411 2.430915e-01 3.956513e+01 1.627582e+02 7.346586 8.675688e-11 2.999685e-09
-
-649 Mir21 26121.31011 4.639963e+04 5.842995e+03 1.259276e-01 -2.989333 1.048681e-10 3.519252e-09
-
-654 Mir214 134.69038 2.546966e+01 2.439111e+02 9.576536e+00 3.259504 1.338023e-10 4.361954e-09
-
-638 Mir200b 87.13638 1.725548e+02 1.717931e+00 9.955853e-03 -6.650239 2.397950e-10 7.600169e-09
-
-666 Mir24-2 424.48288 1.104079e+02 7.385578e+02 6.689355e+00 2.741867 4.542021e-10 1.363802e-08
-
-700 Mir3074-2 424.48288 1.104079e+02 7.385578e+02 6.689355e+00 2.741867 4.542021e-10 1.363802e-08
-
-845 Mir871 33.03360 6.461640e+01 1.450790e+00 2.245235e-02 -5.476990 5.839129e-10 1.708320e-08
-
-767 Mir429 49.75018 9.677270e+01 2.727653e+00 2.818618e-02 -5.148868 6.903556e-10 1.969239e-08
-
-655 Mir215 152.78082 3.329953e+01 2.722621e+02 8.176156e+00 3.031423 8.994273e-10 2.503040e-08
-
-566 Mir148a 118994.46955 2.065090e+05 3.147993e+04 1.524386e-01 -2.713700 1.022762e-09 2.772155e-08
-
-569 Mir150 553.20599 1.318948e+02 9.745171e+02 7.388592e+00 2.885299 1.044721e-09 2.772155e-08
-
-628 Mir1983 14.04997 0.000000e+00 2.809994e+01 Inf Inf 2.859722e-09 7.415778e-08
-
-581 Mir181a-1 59.53826 1.179305e+01 1.072835e+02 9.097179e+00 3.185419 3.537731e-09 8.970115e-08
-
-784 Mir470 18.37716 3.608521e+01 6.691037e-01 1.854232e-02 -5.753034 7.467127e-09 1.852172e-07
-
-630 Mir199a-2 44.84878 7.384673e+00 8.231288e+01 1.114645e+01 3.478512 8.433815e-09 2.047443e-07
-
-550 Mir132 106.46062 2.691980e+01 1.860014e+02 6.909467e+00 2.788574 1.329950e-08 3.161402e-07
-
-76 2610203C20Rik 79.17666 1.649993e+01 1.418534e+02 8.597210e+00 3.103869 1.594438e-08 3.712764e-07
-
-540 Mir125b-1 79.01988 1.649993e+01 1.415398e+02 8.578206e+00 3.100676 1.650666e-08 3.766821e-07
-
-# VOOM top 50
-
- ID logFC AveExpr t P.Value adj.P.Val B
-
-600 Mir192 -6.948883 14.6763803 -42.722954 2.301199e-16 2.625668e-13 27.266471
-
-536 Mir122a -10.426125 8.1698641 -21.722912 2.859682e-12 1.087633e-09 17.760171
-
-568 Mir149 7.030463 6.3160807 20.883835 4.915491e-12 1.402144e-09 17.277609
-
-645 Mir208a 11.015018 3.9395538 23.252407 1.118938e-12 6.383542e-10 17.208662
-
-530 Mir10b 5.130915 12.2628672 18.242023 3.124991e-11 4.963978e-09 16.221503
-
-561 Mir143hg 2.249221 16.2444825 18.082481 3.521739e-11 4.963978e-09 16.026695
-
-560 Mir143 2.251067 16.2358599 18.081481 3.524391e-11 4.963978e-09 16.026084
-
-646 Mir208b 12.433228 4.6076218 19.592458 1.179199e-11 2.690931e-09 15.683666
-
-523 Mir101b -3.765722 10.8508440 -16.538566 1.180419e-10 1.036045e-08 14.900027
-
-796 Mir499 11.567529 3.7874598 17.942086 3.915496e-11 4.963978e-09 14.821741
-
-566 Mir148a -2.638213 15.4435820 -16.548188 1.171186e-10 1.036045e-08 14.814792
-
-844 Mir802 -9.158434 2.9157675 -17.316522 6.338616e-11 7.232360e-09 14.381577
-
-698 Mir3073 -8.420542 2.5457189 -16.702657 1.033066e-10 1.036045e-08 13.985845
-
-649 Mir21 -2.938537 13.1642917 -15.375404 3.148335e-10 2.394833e-08 13.867698
-
-585 Mir181c 3.742560 9.6295577 15.242361 3.537063e-10 2.522368e-08 13.810405
-
-791 Mir490 8.474378 3.7506957 16.259650 1.484816e-10 1.210125e-08 13.424617
-
-663 Mir23a 3.165768 8.7896592 14.631179 6.110682e-10 3.873493e-08 13.269174
-
-586 Mir181d 3.636211 6.3713218 14.317073 8.157508e-10 4.898798e-08 12.956333
-
-642 Mir204 7.684425 4.7751735 15.033484 4.254268e-10 2.855364e-08 12.822427
-
-671 Mir27a 3.106935 9.9255796 13.838251 1.281011e-09 6.960160e-08 12.513086
-
-552 Mir133b 6.493549 1.2544862 13.969968 1.129934e-09 6.446275e-08 11.982684
-
-608 Mir194-2 -5.264136 6.0897615 -13.044012 2.792884e-09 1.448491e-07 11.715753
-
-616 Mir195 3.216595 7.4509350 12.869478 3.332788e-09 1.653353e-07 11.587523
-
-756 Mir378 3.097393 7.3832049 11.684163 1.171371e-08 5.346138e-07 10.329692
-
-672 Mir27b 1.976376 15.0957731 11.756036 1.082197e-08 5.144946e-07 10.127719
-
-1017 Snord104 -2.337374 10.6109024 -11.495675 1.444482e-08 6.339052e-07 10.023395
-
-722 Mir322 3.296618 8.2153415 11.415362 1.580762e-08 6.441605e-07 10.008472
-
-655 Mir215 3.045873 5.7544234 11.148134 2.141822e-08 8.082459e-07 9.753268
-
-628 Mir1983 5.895500 0.9931851 11.445812 1.527548e-08 6.441605e-07 9.749260
-
-344 Dnm3os 3.363344 5.8607432 11.092261 2.283960e-08 8.082459e-07 9.689496
-
-637 Mir200a -6.191561 1.7981309 -11.322172 1.756229e-08 6.909853e-07 9.662295
-
-587 Mir182 -4.903995 7.1511683 -11.074468 2.331304e-08 8.082459e-07 9.658842
-
-582 Mir181a-2 3.048298 6.9414651 11.072128 2.337609e-08 8.082459e-07 9.644017
-
-614 Mir1948 -7.195525 4.5513493 -11.005492 2.524936e-08 8.473388e-07 9.341794
-
-654 Mir214 3.280874 5.4784451 10.768257 3.332555e-08 1.086413e-06 9.318504
-
-571 Mir153 5.963803 1.4386315 10.727082 3.498742e-08 1.093990e-06 9.035569
-
-318 Cyp3a25 -6.318200 1.4888933 -10.698226 3.620443e-08 1.093990e-06 9.024973
-
-464 Gm5441 5.982176 1.4484953 10.692891 3.643436e-08 1.093990e-06 9.000362
-
-541 Mir125b-2 3.077678 7.4316058 10.446668 4.893073e-08 1.431538e-06 8.884250
-
-551 Mir133a-1 5.144671 0.5903264 10.358205 5.447229e-08 1.553822e-06 8.575535
-
-550 Mir132 2.847559 5.3211839 10.110952 7.380297e-08 2.004981e-06 8.531491
-
-13 1110038B12Rik -2.226702 10.8487089 -10.194609 6.655312e-08 1.852125e-06 8.439308
-
-922 Rabggtb -1.935779 9.9874171 -9.928995 9.262821e-08 2.457879e-06 8.133384
-
-569 Mir150 2.938531 7.6297870 9.842102 1.033602e-07 2.620755e-06 8.116464
-
-800 Mir504 5.256127 0.6221088 9.892894 9.693595e-08 2.513725e-06 8.068853
-
-573 Mir155 3.906600 3.9899000 9.732173 1.188627e-07 2.712448e-06 8.046518
-
-666 Mir24-2 2.833979 7.3083691 9.767192 1.136724e-07 2.646944e-06 8.030550
-
-700 Mir3074-2 2.833979 7.3083691 9.767192 1.136724e-07 2.646944e-06 8.030550
-
-664 Mir23b 2.124129 9.8141190 9.806316 1.081569e-07 2.625681e-06 7.979464
-
-631 Mir199b 5.752816 2.8805143 9.823920 1.057683e-07 2.623514e-06 7.979387
-
-Warning messages:
-
-1: In bplt(at[i], wid = width[i], stats = z$stats[, i], out = z$out[z$group == :
-
- Outlier (-Inf) in boxplot 5 is not drawn
-
-2: In bplt(at[i], wid = width[i], stats = z$stats[, i], out = z$out[z$group == :
-
- Outlier (-Inf) in boxplot 7 is not drawn
-
-3: In bxp(list(stats = c(-Inf, -Inf, -0.158608221176912, 0.826586442285183, :
-
- some notches went outside hinges ('box'): maybe set notch=FALSE
-
-4: In par(defpar) : calling par(new=TRUE) with no plot
-
-R version 2.15.1 (2012-06-22)
-
-Platform: x86_64-unknown-linux-gnu (64-bit)
-
-locale:
-
- [1] LC_CTYPE=en_AU.UTF-8 LC_NUMERIC=C LC_TIME=en_AU.UTF-8 LC_COLLATE=en_AU.UTF-8 LC_MONETARY=en_AU.UTF-8 LC_MESSAGES=en_AU.UTF-8 LC_PAPER=C LC_NAME=C LC_ADDRESS=C LC_TELEPHONE=C LC_MEASUREMENT=en_AU.UTF-8 LC_IDENTIFICATION=C
-
-attached base packages:
-
-[1] methods grid stats graphics grDevices utils datasets base
-
-other attached packages:
-
- [1] edgeR_3.0.8 limma_3.14.4 DESeq_1.10.1 lattice_0.20-15 locfit_1.5-9.1 Biobase_2.18.0 BiocGenerics_0.4.0 gplots_2.11.0 MASS_7.3-23 KernSmooth_2.23-10 caTools_1.14 gdata_2.12.0.2 gtools_2.7.1 stringr_0.6.2
-
-loaded via a namespace (and not attached):
-
- [1] annotate_1.36.0 AnnotationDbi_1.20.7 bitops_1.0-5 DBI_0.2-7 genefilter_1.40.0 geneplotter_1.36.0 IRanges_1.16.6 parallel_2.15.1 RColorBrewer_1.0-5 RSQLite_0.11.3 splines_2.15.1 stats4_2.15.1 survival_2.37-4 XML_3.96-1.1 xtable_1.7-1
-
-
-
-
-
-
diff -r 37b851eb8203 -r 48d71bd383a1 rgedgeR/test-data/edgeRtest1out.xls
--- a/rgedgeR/test-data/edgeRtest1out.xls Sat Jul 27 22:28:00 2013 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,1142 +0,0 @@
-Name logFC logCPM LR PValue adj.p.value Dispersion totreads case_X11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam control_X11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam case_X11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam case_X11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam control_X11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam control_X11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam
-Mir122a -10.6613482198735 12.5379487184339 445.912028851371 5.59474310450852e-99 6.38360188224422e-96 0.102055096028295 90428 6.64466912039531 2.86464823551992 20.1236936368881 4.75652253016081 20841.6623198401 16818.9531619257 7242.55663282834 8468.31297344994 12 7 27 8 29767 24233 11911 24463
-Mir192 -7.10901851688288 17.2474145508888 366.131659138235 1.3015583263717e-81 7.42539025195057e-79 0.0776548700185199 2325567 1779.66387941254 1294.41176699279 4493.54625691845 1933.52640851037 463599.032378899 340312.253828562 383591.60517699 182292.180510107 3214 3163 6029 3252 662133 490327 630849 526600
-Mir208b 13.4237202575152 9.82233816515324 355.417815392181 2.80129611458365e-79 1.06542628891331e-76 0.124440587141633 14756 1245.90702213628 570.139045385768 4930.34448733332 881.902421077918 0.74532198655141 0 0 0 2049 1647 8904 2155 1 0 0 0
-Mir208a 11.9775863683342 8.38828977985358 348.815401742963 7.675450754893e-78 2.18942232783323e-75 0.0993679816515115 4638 433.789589950159 712.527819143148 1006.59908044528 649.748467524829 0 0 0 0.553722426699609 1060 956 1693 928 0 0 0 1
-Mir499 14.4882160574998 8.61277040381698 291.127944921827 2.82350748745294e-65 6.4432440863676e-63 0.134816198797062 6527 608.439028317971 506.657690265579 2521.60879492395 270.357373677161 0 0 0 0 869 730 4147 781 0 0 0 0
-Mir149 6.86973108218652 8.78566474384905 253.019861795716 5.70293016120625e-57 1.08450721898939e-54 0.0983468375157501 6164 774.657674952754 459.571424069838 1710.51395913549 766.394692672161 17.5039996639232 6.24646467450714 4.86444908593961 5.5386913941544 1399 1123 2295 1289 25 9 8 16
-Mir490 8.4539298899245 6.90959613094456 251.056095815646 1.52828085290668e-56 2.4910977902379e-54 0.0974500488770791 1741 209.881556643346 217.749755819205 520.538722875595 195.794075709069 1.03850463640395 0.553722426699609 0 0.74532198655141 353 311 750 322 3 1 0 1
-Mir802 -12.4996776940066 6.62939088571757 237.561606597444 1.33781241656995e-53 1.90805495913289e-51 0.10939980863872 1514 0 0 0 0 305.654779538184 164.10342034907 155.772295189245 209.286991327076 0 0 0 0 552 401 209 352
-Mir204 7.37117920479641 7.55899555710097 237.12302218121 1.66736458270285e-53 2.11384776540439e-51 0.10292005004102 2601 425.578854320855 326.416358632286 646.247667592045 375.481932100929 3.04028067871226 0.6923364242693 0.553722426699609 3.68311915995418 571 549 923 541 5 2 1 9
-Mir1948 -7.58332571104735 7.29345576009458 204.796406017043 1.87589722530299e-46 2.14039873407072e-44 0.118339985035871 2404 1.2161122714849 0.6923364242693 1.66116728009883 1.63694184886853 647.684806313175 385.278324943026 181.341436518244 428.229856018989 2 2 3 4 869 648 259 617
-Mir3073 -11.7485555893732 5.88146234349958 200.033500954155 2.05362547312175e-45 2.13016969530174e-43 0.110685621278186 904 0 0 0 0 207.347142288176 75.4646702453536 72.5376378976488 87.5763889144661 0 0 0 0 341 218 131 214
-Mir194-2 -5.43982669183809 7.86004832737241 165.572392495399 6.85919857312405e-38 6.52195464327879e-36 0.106710199302315 3570 10.5207261072926 6.13853193325697 14.9064397310282 9.51304506032163 921.410542308918 600.354660383186 266.936643590936 304.628026678492 19 15 20 16 1316 865 439 880
-Mir10b 5.0328982107069 13.880769769219 160.065802570007 1.0946399286548e-36 9.60757045073175e-35 0.107954343937396 197340 25838.8226297643 32163.6053489474 36317.2985027079 34465.2158674084 1825.38451949884 373.861669105422 658.375965345836 727.211416359842 34668 54096 51870 49658 3002 1080 1189 1777
-Mir101b -3.92528713393055 11.9360901455378 120.624266541894 4.61814317471517e-28 3.76378668739286e-26 0.0966307527814339 59019 219.816814705503 301.225000124588 811.923157038789 427.069498293958 10145.0679915167 7747.97041123897 11280.4211505294 6628.41993572847 635 544 1984 573 17063 11066 16253 10901
-Mir182 -5.24438373094747 8.94270765623571 118.928149724545 1.08592583416118e-27 8.26027584518606e-26 0.149934428671101 7189 16.9622423945978 14.3967830941898 22.0987149597251 31.3035234351592 984.005598427018 615.44062818354 2366.0220083772 653.660345923136 49 26 54 42 1655 879 3409 1075
-Mir200b -6.72534784619757 5.76518685294719 115.731891447532 5.44098879544178e-27 3.88010513474942e-25 0.167124904530932 888 2.43222454296981 0 1.66116728009883 0 369.679705329499 97.5087118682966 46.2105591127573 107.578002727623 4 0 3 0 496 164 66 155
-Mir181c 3.6118671281253 10.5698150360209 107.820107113202 2.94315295097335e-25 1.97537501003564e-23 0.0938527006387662 23605 2420.85208718677 1892.87875056625 4093.0929402801 1902.59025813986 232.036507077113 272.787847077816 228.313081447719 298.968314259808 3488 3113 11824 3436 567 366 384 427
-Mir181d 3.48997562250607 7.2320639569436 102.186614268585 5.05301947727886e-24 3.20305290198621e-22 0.087384984044046 2139 310.053946405387 202.152207531835 539.823349635392 295.665994593338 36.4833681445471 14.5390649096553 25.471231628182 15.550947564251 416 340 771 426 60 42 46 38
-Mir21 -3.07777147203033 13.8815003666918 91.3732407445455 1.1897452302054e-21 7.14473319823348e-20 0.0849427206355669 229120 3207.21258454416 2190.82625708005 4348.9112490476 2010.56613134628 27154.0006244933 33227.944804435 25707.2205795704 35379.0841207216 4621 3603 12563 3631 66353 44582 43237 50530
-Mir199b 5.41147631803522 4.69586911909022 86.7037178851385 1.26059609329233e-20 7.19170071223273e-19 0.156561826531982 370 43.4032680877174 44.8102391396434 99.2493831616134 49.2525469951386 1.3846728485386 0.553722426699609 0 2.98128794620564 73 64 143 81 4 1 0 4
-Mir193 -5.36015662788668 4.77547692611212 84.6612650026128 3.5412053458764e-20 1.92405490459285e-18 0.155464968416992 421 1.49064397310282 1.1891306325402 2.80063994622771 0.694051630500793 101.545374668989 34.9629894255996 33.7770680286762 33.9665433640219 2 2 4 1 167 101 61 83
-Mir23a 3.00307076424737 9.46741956688047 82.28684490401 1.17702908493873e-19 6.10450084506861e-18 0.0892034490333833 10118 1149.88932166638 1127.95773834321 2471.51785621332 1096.32521274364 150.583172278573 126.802435714211 89.2133307633346 243.720289602311 1934 1611 3561 1803 435 229 218 327
-Mir195 3.06054621394571 8.15279745103936 81.3972715690713 1.84612638492429e-19 9.15839219651573e-18 0.0913301572784805 3962 429.134880692197 283.190939854255 922.708619350646 470.89573048592 110.625277875995 77.7337826160888 45.6042101806839 41.540185456158 775 692 1238 792 158 112 75 120
-Ahsg -10.1013431702234 6.6385887851201 79.821328032349 4.09844702296257e-19 1.92375926690416e-17 0.42092199405061 1524 0 0.553722426699609 0 0 348.415275334279 12.6028797580247 610.071383210197 24.3222454296981 0 1 0 0 586 18 879 40
-Mir148a -2.78937502090353 16.047168680842 79.7658888859378 4.21507288979878e-19 1.92375926690416e-17 0.0819605364404836 1002397 15925.5982512306 8528.20007414923 22070.8222058197 10590.1952912549 192723.868638491 105445.564275186 179549.727112645 134274.698694836 26191 24636 39859 25878 258578 177349 256441 193465
-Dnm3os 3.18944316253823 6.61883431628908 79.1961422287326 5.62397892398994e-19 2.46806152010482e-17 0.0949653148790185 1401 134.000827261305 87.167153452249 365.207773410191 182.531552094921 37.1084792875172 24.9858586980285 12.161122714849 13.846728485386 242 213 490 307 53 36 20 40
-Mir27a 2.92177170736328 10.5812768795259 77.2698776994316 1.49123094631961e-18 6.30183151759511e-17 0.0912505912483571 21886 2383.61235292684 2512.17403176626 5321.98790268008 2361.69003122368 328.513633315783 347.737683967355 163.694184886853 566.444709779072 4009 3588 7668 3884 949 628 400 760
-Mir429 -5.34193377949947 4.95110312707712 76.3875799779135 2.33112791050646e-18 9.49934623531384e-17 0.183241171201345 499 1.7836959488103 0.700159986556928 2.08215489150238 1.82416840722736 91.7345762156822 45.405238989368 16.7786539509024 75.2775206416924 3 1 3 3 265 82 41 101
-Mir214 3.12590636489108 6.20234665031187 74.2821251599606 6.77138706168541e-18 2.66419056461485e-16 0.0953276171520653 1048 110.058160569384 56.4254185779479 198.23262875846 93.7149208477231 33.5394893948135 15.4586982230226 11.9027197714678 20.127497284523 181 163 358 229 45 26 17 29
-Mir200a -7.59226302352062 4.05994320136271 73.7142550533581 9.02845045111825e-18 3.43382065490864e-16 0.224178202729185 264 0 0 0.594565316270102 0 90.2267119651031 32.2269751943499 11.4235510004434 26.0249540548816 0 0 1 0 130 53 33 47
-Mir194-1 -3.97021853073367 5.39389876933198 73.2237979529499 1.1575165879669e-17 4.26040782861365e-16 0.130958864780352 635 3.56739189762061 9.10207982524007 5.55241304400634 3.64833681445471 76.1570066696229 88.5955882719375 33.1480724395876 105.090400103749 6 13 8 6 220 160 81 141
-Mir378 2.95431952960146 8.05336780578876 73.0964650986627 1.23465451887634e-17 4.40231501886846e-16 0.0956665499194766 4075 425.697271826612 392.139171232948 1155.9147140464 188.315507401249 76.4136948845461 36.8311915995418 91.6746043458234 63.0239235246308 608 565 1901 544 138 90 123 106
-Mir322 3.05856921521976 8.94824187288921 72.8372126855238 1.40796901194656e-17 4.86815952312432e-16 0.103656954331831 7074 1012.89257972337 671.858807385215 1784.70780573361 855.071608776977 158.70265142878 78.9263523667001 50.3887408296645 91.6687435366374 1359 1130 2549 1232 261 228 91 224
-Mir215 2.90893351586836 6.38192368892387 70.311049912704 5.06531683728474e-17 1.69986073862997e-15 0.0900203619873792 1182 123.075020467911 161.036796908093 272.762290786812 122.219283284233 19.3854198795404 17.1653952276879 11.4585929420797 26.8315915158508 207 230 393 201 56 31 28 36
-Cyp3a25 -9.77860211373653 3.91325729596345 70.0264241191466 5.85153294977192e-17 1.90759974162565e-15 0.264452365698728 226 0 0 0 0 56.6444709779072 17.836959488103 65.1148787497943 18.7393940235214 0 0 0 0 76 30 93 27
-Mir183 -4.21446206828232 5.24792871814947 66.3110130402762 3.85100994568175e-16 1.22055620778413e-14 0.159551640795599 563 8.40191983868314 1.38810326100159 2.43222454296981 2.42317748494255 86.3806985651391 29.0557178174163 134.903279565805 77.2934911151132 12 2 4 7 156 71 181 130
-Mir181a-2 2.83771284942958 7.57379761415609 65.529002601634 5.72650030707276e-16 1.76592887847838e-14 0.0983402987214175 2817 288.826664477665 137.774948429591 639.549402838049 182.109780686623 58.13511495101 41.025006822637 80.5183984540467 56.912233701065 475 398 1155 445 78 69 115 82
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-Gm16023 -4.84906479740497 2.04843453239765 14.9318719681594 0.000111463899395583 0.000752261048033047 0.781248660083243 61 0 0 1.10744485339922 0 11.1798297982712 0 28.7065594488341 2.08215489150238 0 0 2 0 15 0 41 3
-Mir1960 3.96705781998388 1.29508911386833 14.9214563693412 0.000112080962458911 0.000752261048033047 0.41501288861623 36 2.0770092728079 3.87605698689727 6.13853193325697 4.47193191930846 0 0 0.694051630500793 0.608056135742452 6 7 15 6 0 0 1 1
-0610008F07Rik -4.54488558953107 1.15637169454961 14.5761546583671 0.000134607153569803 0.000898168200135353 0.478560111450913 34 0 0 0 0.74532198655141 9.51304506032163 5.60127989245543 3.47025815250396 2.43222454296981 0 0 0 1 16 8 5 4
-Mir30c-1 1.27691626836962 5.65565459422496 14.2837634742279 0.000157215137919935 0.00104292135096887 0.0942811372414155 732 60.0510969432802 62.3142388035666 139.504377730659 69.926455610382 27.3472887586373 28.2398437616801 14.3232411775996 45.464641179636 101 89 201 115 79 51 35 61
-Mir674 1.68665633785934 4.7344282331729 14.2584368876227 0.000159344901134507 0.0010509394924536 0.157762238651678 392 41.025006822637 30.8070394085048 91.6148152261047 31.6189190586075 8.65420530336624 12.1818933873914 4.50159008438844 27.5769135024022 69 44 132 52 25 22 11 37
-Mir328 1.21754727845112 7.37025735114261 14.1902387757875 0.000165225411008837 0.00108346088483381 0.0938897453017011 2362 163.284949424635 204.218224315086 326.416358632286 256.258555079836 210.991695672241 91.8164764971102 43.2710265168312 107.422150779724 399 274 549 366 304 151 125 194
-Mir320 1.26517933587612 6.72859295410854 14.1369883832178 0.000169968606945481 0.00110819531728454 0.099920171450282 1651 126.317396751144 100.329262397505 222.58616040258 99.6700368059297 74.4808541235179 79.0041305744495 47.5652253016081 79.1180784809329 182 165 643 180 182 106 80 113
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-6430411K18Rik 6.22955452291459 0.286828886351783 13.9015924293055 0.000192635189076567 0.00122791480858303 0.63776153052932 17 0.608056135742452 0.6923364242693 2.76861213349805 3.68311915995418 0 0 0 0 1 2 5 9 0 0 0 0
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-Mir1843 -1.2273858117048 7.53264307773502 13.5863749880724 0.00022783317267533 0.00142053360668061 0.100141470001694 2782 86.8065361754348 93.1212782120715 313.711336986358 73.5747924248367 181.392143158556 213.736856706049 241.03968724589 321.233776203658 146 133 452 121 524 386 589 431
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-Il15ra -3.22133002916769 2.39643465026015 13.4947431198339 0.000239232716838616 0.00146755123609065 0.463402149226182 78 1.1891306325402 0 4.16430978300476 0 6.2310278184237 7.75211397379453 13.9140057153825 2.98128794620564 2 0 6 0 18 14 34 4
-Phyhd1 -6.33005597907163 0.461665646645519 13.484507524553 0.000240541262432612 0.00146768759591235 0.689458292350189 20 0 0 0 0 3.04028067871226 0.34616821213465 6.64466912039531 0.818470924434263 0 0 0 0 5 1 12 2
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-Chka -6.25425180950366 0.398258107742989 13.1693882297149 0.000284559622778948 0.00166503861328605 0.681579113159149 20 0 0 0 0 3.68311915995418 0.74532198655141 5.35108784643091 0.700159986556928 0 0 0 0 9 1 9 1
-Mir30b 1.19069161103915 9.3617074750771 13.1387695167483 0.000289247754457723 0.00168383514202175 0.0999778694962593 10011 740.612373334306 385.285220105865 1872.13552467138 475.940842558524 979.353090328553 417.384852021611 312.971513990947 467.096747327034 1218 1113 3381 1163 1314 702 447 673
-1810008I18Rik -6.625452937907 0.757077785058189 13.1114393173091 0.00029349810965095 0.00169184971514696 0.936533639954261 25 0 0 0 0 4.42977941359688 0 11.9251517848226 0.594565316270102 0 0 0 0 8 0 16 1
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-Gm6313 5.88855380399028 -0.0293445513708015 13.0885458924873 0.000297106893178351 0.00170351238752009 0.502615980276399 15 0.818470924434263 0.74532198655141 4.75652253016081 2.80063994622771 0 0 0 0 2 1 8 4 0 0 0 0
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-Mir297c 6.35987297081253 0.398055363685947 12.7928346540932 0.000347949488780715 0.00194612924852351 0.86476711912211 16 4.16195721389071 4.20095991934157 0 1.82416840722736 0 0 0 0 7 6 0 3 0 0 0 0
-Snord68 -1.13457444274774 8.92132519667897 12.7118658261147 0.000363342726950629 0.0020046158463653 0.0936159992954593 7303 159.237377581939 195.464016624962 433.789589950159 280.24106694333 977.465379948047 906.707182591222 558.711562553138 796.553537822612 460 353 1060 376 1644 1295 805 1310
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-Bmp1 -3.97471936953623 1.38701445027206 12.7011339267468 0.000365433914148977 0.0020046158463653 0.543071332932969 39 0 0.700159986556928 0.694051630500793 0 4.50018675775045 1.66116728009883 7.36623831990836 2.23596595965423 0 1 1 0 13 3 18 3
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-Mir34a 1.91945112130955 3.61902087448453 12.6166339601411 0.000382329185895629 0.00206747678249722 0.209108419099582 180 10.2308865554283 20.1236936368881 36.2684842924762 19.604479623594 8.32861956600951 3.64833681445471 3.4616821213465 6.0909466936957 25 27 61 28 12 6 10 11
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-Snord49b -1.26067966372732 6.59754559587082 12.5629346353204 0.000393473367643403 0.00210776109146067 0.111486118172609 1485 36.8630496087463 39.9091192337449 149.915152188171 57.7653328955329 136.044107368917 135.661994541404 50.3359618527072 219.124664046115 62 57 216 95 393 245 123 294
-Ank1 1.35227733675525 11.2588220131714 12.4614990275367 0.000415426418612258 0.00221496048428311 0.135867548702657 33776 2895.96829163896 2268.80140253178 5907.42206540648 3041.79615803784 1106.25277875995 862.012125081985 2438.30510432723 1082.81416755718 5230 5544 7926 5116 1580 1242 4010 3128
-4833418N02Rik -2.07313530572046 3.53931042163891 12.4439824566212 0.000419340681838063 0.00222543124640572 0.244921651041945 170 6.70789787896269 1.7836959488103 9.802239811797 4.16430978300476 20.6739086152434 9.69270993977019 28.2398437616801 10.2308865554283 9 3 14 6 34 28 51 25
-Mir340 -1.24781368093967 8.59679560345445 12.360285434567 0.000438563635265595 0.0023166717955465 0.11588698056633 5906 175.120167093826 82.3880344880466 585.838327448187 100.671923705414 896.622349821346 438.789203407335 966.220781448561 524.008981028099 288 238 1058 246 1203 738 1380 755
-Pknox1 -5.96867464377884 0.108276776805556 12.3202806513909 0.00044806332818544 0.00235594588691054 0.585510339236401 16 0 0 0 0 3.32233456019766 0.818470924434263 5.21725390585987 0.594565316270102 0 0 0 0 6 2 7 1
-Mir3107 1.3508075738813 10.2573409434783 12.2375775967787 0.000468365962224657 0.00245140166467126 0.137805722557386 16873 1553.00460609751 1938.04284278958 2747.75040515264 1553.58342682196 273.126719374239 343.861626980457 820.517101745348 1165.68358696641 2612 2768 3959 2555 789 621 2005 1564
-Mir486 1.35080726179605 10.2573415082787 12.2166008121444 0.000473661512742678 0.00246779810976893 0.13804319607134 16873 1828.8178848867 1921.13491322619 2407.29424140437 884.45978200403 436.886994665992 254.135222036839 1494.37058303558 929.900154646439 2612 2768 3959 2555 789 621 2005 1564
-Gm15787 -5.84922159415344 -0.0267336728102733 12.0781096044983 0.000510173001972336 0.0026459427056838 0.520917363420797 14 0 0 0 0 1.10744485339922 2.45541277330279 1.49064397310282 2.37826126508041 0 0 0 0 2 6 2 4
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-Snord1a -1.79805603420245 3.92918303968764 11.9925876763572 0.000534125716115637 0.00274521370309884 0.200145509933857 230 4.9011199058985 6.24646467450714 16.4175156650462 2.7693456970772 34.3307904553758 22.0987149597251 23.8503035696451 18.4315248043731 7 9 27 8 62 54 32 31
-Snord42b -1.18512884296518 6.24789852349338 11.9040618509162 0.000560116711777104 0.00285518663749724 0.101627779377629 1095 48.5836141350555 40.1317049590018 30.4628026678492 45.9589614160676 92.8964499232888 170.678734920273 81.4554483290039 136.531197378601 70 66 88 83 227 229 137 195
-Snhg7 -2.34268751527016 3.5610429386213 11.9026964396979 0.000560527438036267 0.00285518663749724 0.338566530531322 173 2.21488970679844 1.22770638665139 11.1798297982712 4.16195721389071 23.8054395429356 10.4107744575119 49.860603130881 4.50018675775045 4 3 15 7 34 15 82 13
-1700001L05Rik -5.950973384031 0.0930486569679726 11.7459555862755 0.000609755940371602 0.00309214012428443 0.654968245797187 16 0 0 0 0 4.47193191930846 0 4.20095991934157 2.77620652200317 0 0 0 0 6 0 6 4
-Rnf44 -3.56352892254898 2.54220698820135 11.7368125443015 0.000612758782003269 0.00309361845250323 0.670391576244117 88 0.818470924434263 1.49064397310282 1.1891306325402 0 22.2096521760254 0 15.9237377581939 2.21488970679844 2 2 2 0 32 0 46 4
-Trmt61b -6.04462877508772 0.197297525490101 11.686250899599 0.000629636409648177 0.00316482442030207 0.741746117911198 18 0 0 0 0 6.68861749316697 0.6923364242693 2.76861213349805 0 0 0 0 0 11 2 5 0
-Def8 -5.9906404918121 0.123717443385779 11.628655678048 0.000649434749337637 0.0032500221447116 0.700504873096256 16 0 0 0 0 1.73084106067325 0.553722426699609 3.68311915995418 0.74532198655141 0 0 0 0 5 1 9 1
-Mir878 -5.70475205457436 -0.1626146032132 11.6151126935116 0.000654180742215014 0.00325947697321978 0.47390488168473 13 0 0 0 0 1.22770638665139 0.74532198655141 2.97282658135051 2.80063994622771 0 0 0 0 3 1 5 4
-Mir511 -1.91950371805125 3.59489884941376 11.5870640997842 0.000664121779537945 0.0032946215237078 0.22775643116366 183 4.9011199058985 6.24646467450714 9.72889817187923 1.3846728485386 31.5621783218777 14.3232411775996 14.1611177444768 21.4043513857237 7 9 16 4 57 35 19 36
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-Mir335 1.11656851457955 6.55078457560659 11.3673264027419 0.000747473949853804 0.00367615421027237 0.0963844774767941 1318 137.884567512011 120.696759202831 200.245756155281 135.340067947655 83.9117467324583 34.9629894255996 39.8680147223719 56.4744937859641 185 203 286 195 138 101 72 138
-Mir210 1.3815129543114 5.22746528492104 11.3305689566611 0.000762415382904168 0.00373354485791268 0.14042671192209 592 60.3710809106642 26.7554392321546 170.83903671989 40.9490461995468 42.5639295019716 6.92336424269299 20.4877297878855 14.7324766398167 81 45 244 59 70 20 37 36
-4931408D14Rik -6.38756698788491 0.523260717236992 11.280671896319 0.00078318206252862 0.00381884928779981 1.07304045821678 22 0 0 0 0 5.53722426699609 0 8.94386383861692 0 0 0 0 0 10 0 12 0
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-Snord83b -0.576387059675669 3.89404617232097 1.39650694760333 0.237309298047112 0.333738123904012 0.188423727901865 221 15.4035197042524 8.32861956600951 21.2819647509858 5.5386913941544 26.5786764815813 9.00318016877689 25.3409475427479 19.0260901206433 22 12 35 16 48 22 34 32
-Orc6 -1.65891001544319 -1.53143456249569 1.39410757284254 0.237712651897134 0.333738123904012 0.346829941720672 5 0.553722426699609 0 0 0 0.700159986556928 0.694051630500793 0.608056135742452 0.34616821213465 1 0 0 0 1 1 1 1
-Nnt -0.943384996373025 3.06429209846151 1.3928418650093 0.237925762385849 0.333738123904012 0.530661278894176 121 7.63456793550872 6.08056135742452 2.42317748494255 4.42977941359688 14.3232411775996 0 26.1608739158845 4.20095991934157 11 10 7 8 35 0 44 6
-1700113A16Rik -1.25132935558282 -0.405410492935541 1.39185622273126 0.238091878052468 0.333738123904012 0.335679278399479 11 0.74532198655141 0 0.700159986556928 0.694051630500793 1.2161122714849 0.34616821213465 1.10744485339922 1.22770638665139 1 0 1 1 2 1 2 3
-Snord111 -0.768354560924835 2.44255708268487 1.37937795879974 0.240207131983939 0.336289984777514 0.302987417663513 82 4.20095991934157 2.77620652200317 7.90472976465187 2.0770092728079 12.735615814091 5.72929647103984 7.4532198655141 3.56739189762061 6 4 13 6 23 14 10 6
-Mir377 1.61685029109297 -0.764927019547182 1.3719133201312 0.241483420704625 0.337338320076739 0.871922904191011 8 0.34616821213465 0 0.409235462217131 2.98128794620564 0 1.40031997311386 0 0 1 0 1 4 0 2 0 0
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-Ubl4 -1.27034177587966 0.0534863754405797 1.3565087782031 0.244143458366216 0.340131484732421 0.571194645489501 15 0.34616821213465 0 0.409235462217131 1.49064397310282 1.7836959488103 0 3.47025815250396 1.82416840722736 1 0 1 2 3 0 5 3
-Mirlet7a-1 -0.479655320722763 4.78553688143684 1.34788689468875 0.24564787267199 0.341810027705781 0.142907204927484 419 17.6336279365311 8.30803709123159 49.2812959762652 13.0955347909482 61.861724883767 34.4847883436659 25.2057595160494 47.1955108740539 29 24 89 32 83 58 36 68
-Gm2518 -1.39162129449246 -0.884936739010693 1.34396740253008 0.246335518812973 0.342349362930088 0.381243283650106 8 0 0.74532198655141 0.594565316270102 0 1.38810326100159 0 0.6923364242693 1.10744485339922 0 1 1 0 2 0 2 2
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-Mir26a-2 -0.715034883511368 3.11546420527345 1.32372336809166 0.249924914221204 0.346493714612873 0.304126393558787 131 4.09235462217131 2.23596595965423 18.4315248043731 5.60127989245543 11.7988777185135 17.6336279365311 3.80785033348115 12.1818933873914 10 3 31 8 17 29 11 22
-Gm13375 -1.6921982855423 -1.49322451341955 1.31837615791593 0.250883687602521 0.347400834410773 0.549500512407157 5 0 0 0 0.553722426699609 0 0.74532198655141 1.1891306325402 0.700159986556928 0 0 0 1 0 1 2 1
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-Rnf126 -1.6247427069646 -1.5483229499814 1.31264181313975 0.251916897228801 0.347986900409276 0.388474138185462 5 0.700159986556928 0 0 0 1.10744485339922 0.409235462217131 0.74532198655141 0 1 0 0 0 2 1 1 0
-Mir223 0.392453416059884 5.98833711727872 1.3035785418167 0.253560594977612 0.349555682071357 0.104178045605271 928 40.1050752972789 81.2400965341037 127.236977681802 65.1148787497943 82.5921440295944 62.6297819814725 18.3469152431364 76.9674173112457 98 109 214 93 119 103 53 139
-Snord8 -0.978027022403874 1.09887870775351 1.30298812584026 0.25366812862396 0.349555682071357 0.4314327128184 32 0.74532198655141 1.7836959488103 2.80063994622771 1.38810326100159 6.08056135742452 1.3846728485386 3.32233456019766 0.818470924434263 1 3 4 2 10 4 6 2
-F420014N23Rik -1.372332867125 0.486804153233623 1.30132325747801 0.253971656824851 0.349555682071357 0.978195779320001 22 0 1.2161122714849 1.3846728485386 0 3.27388369773705 0 4.75652253016081 0 0 2 4 0 8 0 8 0
-F630028O10Rik 0.392450488800123 5.98834207543087 1.29739234247459 0.25469009215405 0.35012216282864 0.104716472119336 928 73.0415546820382 64.8076194734411 149.834237123183 64.5468016365737 72.3586801533518 35.6553258498689 29.3472886150793 56.8837292481813 98 109 214 93 119 103 53 139
-Mir1945 -1.60978084536385 -1.55009830160392 1.29570121271995 0.254999942083813 0.35012627426911 0.378858489230937 5 0 0.553722426699609 0 0 1.1891306325402 0 0.694051630500793 0.608056135742452 0 1 0 0 2 0 1 1
-Mir3082 0.661138784925018 2.97567078622387 1.29273748445739 0.255544079405897 0.350451676204481 0.24963376787416 112 9.12084203613678 4.1540185456158 13.2893382407906 6.5477673954741 7.4532198655141 7.72934911151132 7.70175985212621 7.63456793550872 15 12 24 16 10 13 11 11
-Klc2 -1.65680060376313 -1.51683877037243 1.27647893144847 0.258554746351741 0.354154820633057 0.529733958421577 5 0 0 0 0.594565316270102 0.700159986556928 1.38810326100159 0.608056135742452 0 0 0 0 1 1 2 1 0
-Rmi1 -1.45414479134642 -0.862825068790834 1.26709959878699 0.260311499173742 0.356039233357995 0.605978592018314 8 0.553722426699609 0 0.74532198655141 0 0.700159986556928 0 2.43222454296981 0.34616821213465 1 0 1 0 1 0 4 1
-Mir134 1.03495548835917 1.45319323033477 1.26580803072866 0.260554566042004 0.356039233357995 0.601898706633359 40 1.38810326100159 3.64833681445471 3.4616821213465 4.42977941359688 2.86464823551992 5.21725390585987 0 0 2 6 10 8 7 7 0 0
-C230037L18Rik -1.62980533639894 -1.52772398832634 1.2624738205075 0.261183349066953 0.35647153263803 0.484879154690579 5 0 0.700159986556928 0 0 0.34616821213465 0 0.409235462217131 1.49064397310282 0 1 0 0 1 0 1 2
-Mir3060 1.08677713577326 0.277864369948646 1.25611314182789 0.262388104130247 0.357668836230783 0.473324331323197 19 0.34616821213465 0.553722426699609 3.27388369773705 2.23596595965423 1.7836959488103 0.700159986556928 0 1.2161122714849 1 1 8 3 3 1 0 2
-4930562F07Rik -1.64522099748687 -0.476339007188187 1.25291626650739 0.262996216290631 0.357668836230783 1.1878443646274 10 0 0.818470924434263 0 0 1.40031997311386 0 3.64833681445471 0 0 2 0 0 2 0 6 0
-Mir299 0.843754595626436 1.52663929643581 1.25289109673179 0.263001011040865 0.357668836230783 0.353242653337154 43 4.85836141350555 3.04028067871226 4.1540185456158 1.66116728009883 2.86464823551992 2.98128794620564 1.1891306325402 2.10047995967078 7 5 12 3 7 4 2 3
-Myeov2 -1.69291253107605 -1.64496689941108 1.24473900338444 0.264559683155445 0.359360236286146 0.683475557730936 5 0 0 0.34616821213465 0 1.22770638665139 0 0.594565316270102 0 0 0 1 0 3 0 1 0
-Pvt1 -1.32096490868673 -0.847731465862789 1.23855062742672 0.265750566194178 0.360548627856786 0.35441856020169 8 0.553722426699609 0 0 0.594565316270102 1.40031997311386 0.694051630500793 1.2161122714849 0.34616821213465 1 0 0 1 2 1 2 1
-Snora44 -0.381633059781074 5.65314644811287 1.22201591534437 0.268965390360777 0.364170733203647 0.102330578596002 724 52.7479239180603 44.388097909199 28.0396251829066 32.1159007485773 65.0684384925239 61.1164028972156 63.6184888409009 61.6140788170097 76 73 81 58 159 82 107 88
-Mir16-1 -0.412537352408144 5.07566733928455 1.22153990110487 0.269058657397611 0.364170733203647 0.116318778939368 499 21.5951746412848 13.9140057153825 64.8430128299727 27.9445698646948 66.5151987229082 49.2776657655563 30.4028067871226 26.3087841222334 39 34 87 47 95 71 50 76
-Snord92 -0.710096609221731 2.83572908658428 1.2111718792087 0.271100158349136 0.36649914772081 0.316545752043228 106 6.30143987901235 3.47025815250396 10.3369543076217 2.7693456970772 12.735615814091 3.27388369773705 21.6143376099909 4.16195721389071 9 5 17 8 23 8 29 7
-Gm16973 -1.47669981296583 -1.00488414037259 1.16547208604198 0.280333561977 0.378533247592612 0.807783550728712 8 0 0 1.10744485339922 0 2.98128794620564 0 1.40031997311386 0 0 0 2 0 4 0 2 0
-Mir196b 1.25717008543347 -0.50306250554666 1.14571235013042 0.284448506905949 0.383635634018544 0.561933397726954 10 1.10744485339922 0 1.49064397310282 1.7836959488103 0 0.694051630500793 0 0.6923364242693 2 0 2 3 0 1 0 2
-2310040G24Rik -1.45685241958596 -1.01497652446792 1.14394094950534 0.284821122578047 0.383684652729105 0.794086796420206 8 0 0 1.49064397310282 0 2.80063994622771 0 0 0.6923364242693 0 0 2 0 4 0 0 2
-Pafah1b1 -0.979759016418312 1.50245301128808 1.12270570223865 0.289336591381148 0.389307842884304 0.597146443197918 40 1.03850463640395 1.66116728009883 0.818470924434263 2.98128794620564 4.75652253016081 0 11.1048260880127 2.43222454296981 3 3 2 4 8 0 16 4
-E030003E18Rik -1.37677029350632 -0.911606444076738 1.10868384048074 0.292368231420679 0.392923618434623 0.650179476705915 8 0 0 0.409235462217131 0.74532198655141 1.7836959488103 0 2.08215489150238 0 0 0 1 1 3 0 3 0
-Gm11696 -1.6474567394522 -1.48131673919125 1.08635659782644 0.297279881147042 0.399054522810324 0.900717839549015 5 0 0.700159986556928 0 0 0 0.553722426699609 0 2.23596595965423 0 1 0 0 0 1 0 3
-4930568G15Rik -1.63434903676238 -1.50910322195022 1.07512093530211 0.299791605870636 0.401953257694942 0.88678752728023 5 0.34616821213465 0 0 0 0.594565316270102 0 2.08215489150238 0 1 0 0 0 1 0 3 0
-Snord35b -1.11151028366679 0.0545541991626386 1.03680869845452 0.308564847475744 0.413230623204019 0.579271233846859 15 1.22770638665139 0.74532198655141 0 0 3.47025815250396 0.608056135742452 0.6923364242693 1.66116728009883 3 1 0 0 5 1 2 3
-Gt(ROSA)26Sor 1.01120227557646 0.983570556736739 1.03355528158596 0.309325094602678 0.413344830354892 0.651740514579554 26 1.22770638665139 6.70789787896269 0.594565316270102 2.10047995967078 2.08215489150238 0 1.3846728485386 1.66116728009883 3 9 1 3 3 0 4 3
-Wbscr25 1.57399341703069 -1.78130174790484 1.03334353864081 0.309374658302435 0.413344830354892 0.638146949527696 4 1.49064397310282 0.594565316270102 0 0 0 0 0.553722426699609 0 2 1 0 0 0 0 1 0
-Irf3 -1.5346761545771 -1.58329226164049 1.02731268498339 0.310790677441742 0.414751067790676 0.697639468549404 5 0.694051630500793 0 0 0 1.22770638665139 0 0.594565316270102 0 1 0 0 0 3 0 1 0
-Fam172a -1.03402893186865 0.604002126955515 1.018576530994 0.312856898096335 0.417020701784951 0.636367573855024 23 0.594565316270102 0.700159986556928 2.08215489150238 1.2161122714849 2.7693456970772 0.553722426699609 2.86464823551992 0 1 1 3 2 8 1 7 0
-A630010A05Rik 0.949572488616649 0.718313836775746 1.00067217278155 0.317147916372748 0.421790112728613 0.536546495626548 24 1.49064397310282 3.56739189762061 3.50079993278464 1.38810326100159 3.04028067871226 0.34616821213465 0 1.22770638665139 2 6 5 2 5 1 0 3
-2610027K06Rik -1.27624242575249 -0.359242963660928 0.999807031473748 0.31735720510257 0.421790112728613 0.831448038206786 11 0 1.1891306325402 0.700159986556928 0 0.608056135742452 0 3.32233456019766 0.409235462217131 0 2 1 0 1 0 6 1
-Mrpl48 -1.11768365627351 -0.384442829883447 0.999035494819305 0.317544002483679 0.421790112728613 0.464594138402513 11 1.40031997311386 0.694051630500793 0 0 1.66116728009883 0.409235462217131 0.74532198655141 1.7836959488103 2 1 0 0 3 1 1 3
-Chkb -0.980518104316082 0.868956035555252 0.988376398728009 0.320139520836939 0.424490647681999 0.616914850952162 28 1.49064397310282 1.1891306325402 1.40031997311386 1.38810326100159 8.51278590039432 0.6923364242693 2.21488970679844 0 2 2 2 2 14 2 4 0
-B630019K06Rik -1.29011544235618 -1.11663074558135 0.987634695173225 0.320321163588257 0.424490647681999 0.543899136641392 7 0 0 1.2161122714849 0 0.553722426699609 0 1.49064397310282 1.1891306325402 0 0 2 0 1 0 2 2
-Mir25 -0.307341631802256 10.3901562647106 0.978979592374074 0.322450858265771 0.426817203342511 0.0921044561482298 19593 629.333809660793 783.517233779947 1435.5980014577 1349.03279565805 1755.75137894561 1426.22589261646 2371.57442142121 1602.22791768136 1818 1415 3508 1810 2953 2037 3417 2635
-Snord98 -0.405906224465692 5.17577368514848 0.966419614738753 0.325574742787118 0.430452817520395 0.148055095733361 553 24.3637867747828 9.82165109321115 111.798297982712 19.0260901206433 51.8118390052127 53.4419755485611 58.3733890312754 19.3854198795404 44 24 150 32 74 77 96 56
-1600002D24Rik 1.27011387184163 -1.04585152517957 0.961158554000621 0.326895153468287 0.431587161501975 0.571178325056528 7 0 0.694051630500793 1.2161122714849 0.6923364242693 0 0 1.49064397310282 0 0 1 2 2 0 0 2 0
-Map1lc3a -1.14709638433051 0.508393686785022 0.959990722198208 0.32718921533673 0.431587161501975 0.906355460018944 21 0.74532198655141 0 1.40031997311386 2.08215489150238 3.64833681445471 0 4.98350184029649 0 1 0 2 3 6 0 9 0
-8430429K09Rik -1.3414156662313 -0.646531504052733 0.95101637800707 0.329460721920131 0.434081620913244 1.09628514397537 11 0 0 1.03850463640395 0 2.86464823551992 0 0.594565316270102 0 0 0 3 0 7 0 1 0
-Mir505 -0.943456398194506 0.15617379176166 0.947097472025823 0.330459212871538 0.434894996408795 0.393870389120889 16 1.38810326100159 0.608056135742452 0.34616821213465 0.553722426699609 1.22770638665139 1.49064397310282 1.1891306325402 2.80063994622771 2 1 1 1 3 2 2 4
-2210015D19Rik -1.68603662544734 -1.44669874969517 0.944398994380489 0.331149094714323 0.435300826116408 1.44754483144648 5 0.74532198655141 0 0 0 0 0 2.21488970679844 0 1 0 0 0 0 0 4 0
-Gm9776 -1.40607274664126 -1.117570120137 0.909181557848226 0.340331668786721 0.446856656024912 1.04170396479238 7 0 0 1.2161122714849 0 0.553722426699609 1.63694184886853 0 0 0 0 2 0 1 4 0 0
-Gm10336 1.46642692596801 -1.85743790875601 0.903427148882018 0.341864425738265 0.447838472752423 0.638146949527696 4 0 0 0.700159986556928 1.38810326100159 0 0 0 0.409235462217131 0 0 1 2 0 0 0 1
-Gm16897 1.46642692596801 -1.85743790875601 0.903427148882018 0.341864425738265 0.447838472752423 0.638146949527696 4 0 0 0.608056135742452 0.6923364242693 0 0 0 0.594565316270102 0 0 1 2 0 0 0 1
-Mir32 -0.44118887598408 4.19350189789183 0.898649650574614 0.343144047653345 0.448620773316011 0.176547126031611 274 10.5207261072926 5.32006100882271 40.9927092603276 16.6478288555628 33.6076793547326 24.9858586980285 17.6336279365311 15.9237377581939 19 13 55 28 48 36 29 46
-4930474G06Rik 1.46102259696366 -1.84717448236549 0.896800174910108 0.343641153267479 0.448620773316011 0.638146949527696 4 0.409235462217131 0.74532198655141 0.594565316270102 0 0 0 0.34616821213465 0 1 1 1 0 0 0 1 0
-A430093F15Rik 1.46102259696366 -1.84717448236549 0.896800174910108 0.343641153267479 0.448620773316011 0.638146949527696 4 0.553722426699609 0.409235462217131 0.74532198655141 0 0 0 0.608056135742452 0 1 1 1 0 0 0 1 0
-Mir872 -0.31739399651627 5.84043746331986 0.886164346084638 0.346518854683679 0.451860586507517 0.0990643765497606 859 43.7800417734565 22.8471020008869 90.8104779787359 27.8280114307649 135.648601552357 73.7260992174926 45.5103991262003 81.8980923990936 72 66 164 68 182 124 65 118
-Fam19a2 1.4480882584731 -1.85004212492862 0.882418462846213 0.347540136529334 0.452674995182614 0.638146949527696 4 0.694051630500793 0 0.34616821213465 0.553722426699609 0 0.74532198655141 0 0 1 0 1 1 0 1 0 0
-Nol8 -1.14310540598069 -0.147512884347668 0.880430696423492 0.348083742288729 0.452866077481687 0.84067895002272 14 0 0 1.40031997311386 1.38810326100159 3.64833681445471 0 2.21488970679844 0 0 0 2 2 6 0 4 0
-Mir501 -0.507499478420336 4.85304180354494 0.872779448711603 0.350186987306599 0.455083545007779 0.260597386343111 395 37.699480416032 12.4620556368474 4.42977941359688 13.9140057153825 53.6631830317015 39.2413108738267 20.3046396101509 61.0765434840698 62 36 8 34 72 66 29 88
-Gm6225 -1.33737355871558 -0.76777742001415 0.847486445177161 0.357264384067252 0.463238955378804 1.06898496044319 8 0 0 0 1.38810326100159 0 1.03850463640395 0 1.22770638665139 0 0 0 2 0 3 0 3
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-Plscr3 0.0814004336200907 -1.89261335490638 0.00301642056831319 0.956200644868514 0.968047332759487 0.638146949527696 4 0 0.74532198655141 0.594565316270102 0 0.694051630500793 0.608056135742452 0 0 0 1 1 0 1 1 0 0
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-Mir1966 0.000918355090882732 -0.94191710317151 1.38947096530728e-05 0.997025843661245 0.997900427734632 0.449008936327196 8 0 0.34616821213465 1.66116728009883 0 1.49064397310282 0.594565316270102 0.700159986556928 0 0 1 3 0 2 1 1 0
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diff -r 37b851eb8203 -r 48d71bd383a1 rgedgeR/test-data/gentestdata.sh
--- a/rgedgeR/test-data/gentestdata.sh Sat Jul 27 22:28:00 2013 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,9 +0,0 @@
-#!/bin/bash
-# generate test data for rgGSEA
-# ross lazarus June 2013
-# adjust gseajar_path !
-GSEAJAR_PATH=/home/rlazarus/galaxy-central/tool_dependency_dir/gsea_jar/2.0.12/fubar/rg_gsea_test/8e291f464aa0/jars/gsea2-2.0.12.jar
-python ../rgGSEA.py --input_tab "gsea_test_DGE.xls" --adjpvalcol "5" --signcol "2" --idcol "1" --outhtml "gseatestout.html" --input_name "gsea_test" --setMax "500" --setMin "15" --nPerm "10" --plotTop "20" --gsea_jar "$GSEAJAR_PATH" --output_dir "gseatestout" --mode "Max_probe"
---title "GSEA test" --builtin_gmt "gseatestdata.gmt"
-
-
diff -r 37b851eb8203 -r 48d71bd383a1 rgedgeR/test-data/test_bams2mx.xls
--- a/rgedgeR/test-data/test_bams2mx.xls Sat Jul 27 22:28:00 2013 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,3243 +0,0 @@
-Contigname 11706Liv_CAAAAG_L003_R1_001_trimmed.fastq_bwa.sam.bam 11706He_AGTTCC_L001_R1_001_trimmed.fastq_bwa.sam.bam 11699He_GGCTAC_L001_R1_001_trimmed.fastq_bwa.sam.bam 11698He_TAGCTT_L001_R1_001_trimmed.fastq_bwa.sam.bam 11700Liv_ATTCCT_L003_R1_001_trimmed.fastq_bwa.sam.bam 11698Liv_ACTGAT_L003_R1_001_trimmed.fastq_bwa.sam.bam 11699Liv_ATGAGC_L003_R1_001_trimmed.fastq_bwa.sam.bam 11700He_CTTGTA_L001_R1_001_trimmed.fastq_bwa.sam.bam
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-Snord83b 48 22 12 35 22 34 32 16
-Snord85 3804 911 737 1422 3047 1133 3156 882
-Snord87 390 145 138 190 235 255 215 191
-Snord88a 96 69 73 77 62 101 59 52
-Snord88c 74 29 22 35 41 65 52 23
-Snord89 13 2 2 3 2 8 3 3
-Snord90 43 2 3 46 14 48 10 5
-Snord91a 363 40 29 81 256 358 285 25
-Snord92 23 9 5 17 8 29 7 8
-Snord93 45 54 50 161 29 34 29 33
-Snord95 708 217 195 326 483 675 444 210
-Snord96a 145 16 22 56 71 106 59 12
-Snord98 74 44 24 150 77 96 56 32
-Snord99 931 126 80 847 655 668 555 108
-Sox2ot 0 1 0 1 0 0 0 0
-Speer1-ps1 0 0 0 0 0 0 0 0
-Speer5-ps1 0 0 0 0 0 0 0 0
-Speer6-ps1 0 0 0 0 0 0 0 0
-Speer7-ps1 0 0 0 0 0 0 0 0
-Speer8-ps1 0 0 0 0 0 0 0 0
-Speer9-ps1 1 0 0 0 0 0 0 0
-Spn-ps 0 0 0 0 0 0 0 0
-Spns1 5 0 0 1 1 1 0 1
-Sprr2g 0 0 0 0 0 0 0 0
-Sprr2j-ps 0 0 0 0 0 0 0 0
-Sqrdl 35 1 0 1 4 58 3 0
-Sra1 7 0 0 0 2 4 6 0
-Srsf3 7 2 8 2 11 9 14 4
-Srsf7 1 1 0 0 0 5 0 1
-Srsf9 1 2 0 1 0 7 0 3
-St18 0 0 0 0 0 0 0 0
-St5 7 3 0 1 2 7 2 2
-St7l 8 1 1 1 3 12 4 2
-Stap2 10 0 2 2 1 6 4 0
-Stmn1-rs1 0 0 0 0 0 0 0 0
-Stoml1 0 0 0 0 0 0 0 0
-Stxbp3b 0 0 0 0 0 0 0 0
-Surf1 3 0 0 2 3 7 5 0
-Suv39h2 0 0 0 0 0 0 0 0
-Svip 1 0 2 0 0 1 0 0
-Syce2 6 0 0 0 0 19 1 0
-Sycp1-ps1 0 0 0 0 0 0 0 0
-Szrd1 40 4 0 2 16 40 4 2
-Taf1b 1 1 1 0 0 0 0 0
-Taf1d 357 53 56 156 174 341 230 54
-Tardbp 18 0 1 3 7 20 3 0
-Tbrg3 1 1 0 0 0 0 0 0
-Tcp10a 0 0 0 0 0 0 0 0
-Terc 22 1 0 0 18 10 15 0
-Thap6 2 0 2 2 1 1 0 0
-Tk2 1 2 0 2 1 1 3 0
-Tmem161b 0 0 0 0 2 2 4 0
-Tmem179b 8 0 0 0 0 8 0 0
-Tmem181b-ps 0 0 0 0 0 0 0 0
-Tmem181c-ps 0 0 0 0 0 0 0 0
-Tmem194b 0 0 1 0 1 0 0 0
-Tmem205 35 2 0 1 4 57 6 1
-Tmem41a 7 0 0 0 0 5 2 0
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-Tor2a 2 0 0 0 0 11 3 0
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-Trappc13 1 0 0 1 0 0 3 1
-Trim30e-ps1 0 0 0 0 0 0 0 0
-Trim52 0 0 0 0 0 0 0 0
-Trmt61b 11 0 0 0 2 5 0 0
-Trpc4 1 4 1 1 0 0 1 0
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-Trub2 0 0 0 0 0 0 0 0
-Tsix 0 0 0 0 0 4 0 0
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-Tsr2 0 0 1 0 0 2 0 0
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-Tubgcp4 2 2 0 1 0 7 1 0
-Tug1 18 3 0 16 2 27 6 6
-Tyms 0 0 0 0 0 0 1 1
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-Tyw5 1 1 0 0 0 0 0 1
-U05342 20 0 1 3 3 24 3 0
-U90926 0 0 0 0 0 0 0 0
-Ube2w 3 1 2 1 1 3 1 0
-Ubl4 3 1 0 1 0 5 3 2
-Ubxn11 0 0 0 0 0 0 0 0
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-Uqcc 5 0 2 1 0 8 1 1
-Vash2 0 0 0 0 0 0 0 0
-Vaultrc5 243 258 161 383 159 262 286 270
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-Vmn2r-ps60 0 0 0 0 0 0 0 0
-Vmn2r29 2 0 0 0 0 0 0 0
-Vps39 3 1 0 0 0 8 0 0
-Vsig8 194 50 35 100 99 74 109 50
-Wac 15 0 0 0 2 15 2 2
-Wbscr25 0 2 1 0 0 1 0 0
-Wdr13 2 2 1 3 0 1 0 3
-Wdr73 4 0 0 0 0 2 1 0
-Wiz 10 0 1 6 1 3 3 2
-Wls 1 1 0 3 2 0 0 1
-Wwp1 40 0 2 2 4 56 10 4
-Xist 0 0 0 0 0 8 0 0
-Yaf2 2 0 0 0 0 6 0 2
-Yars2 1 0 0 0 1 1 0 0
-Yipf2 1 0 0 1 0 10 0 0
-Ythdf3 16 4 1 4 3 19 3 2
-Zbtb24 1 0 0 1 0 0 0 0
-Zc3h14 11 1 0 0 1 2 2 2
-Zc3h7a 336 148 60 20 17 99 14 60
-Zf12 0 0 0 0 0 0 0 0
-Zfa-ps 0 0 0 0 0 0 0 0
-Zfhx2as 0 0 0 0 0 1 0 0
-Zfp133-ps 0 0 0 0 0 0 0 0
-Zfp207 5 0 2 0 0 9 1 2
-Zfp326 7 2 1 1 0 4 4 0
-Zfp389 0 0 0 0 0 0 0 0
-Zfp410 10 0 2 0 0 6 2 0
-Zfp414 1 0 0 0 0 4 0 0
-Zfp57 0 0 0 0 0 0 0 0
-Zfp572 0 0 0 0 0 0 0 0
-Zfp672 0 0 0 0 0 2 0 0
-Zfp783 0 0 0 0 0 0 0 0
-Zfp809 7 1 0 0 0 4 2 0
-Zfp821 0 0 0 2 2 0 0 0
-Zfp862 4 0 0 0 0 10 2 0
-Zim3 0 0 0 0 0 0 0 0
-Zmynd8 3 5 4 4 3 8 2 1
-Znf41-ps 0 0 0 0 0 0 0 0
-Zp4-ps 0 0 0 0 0 0 0 0
-Zscan4a 0 0 0 0 0 0 0 0
-Zxda 0 0 0 0 0 0 0 0
diff -r 37b851eb8203 -r 48d71bd383a1 rgedgeR/tool_dependencies.xml
--- a/rgedgeR/tool_dependencies.xml Sat Jul 27 22:28:00 2013 -0400
+++ /dev/null Thu Jan 01 00:00:00 1970 +0000
@@ -1,35 +0,0 @@
-
-
-
-
- package_ghostscript_9_07
-
-
-
-
-
-
-
-
-
-
-
-
-
-
- $INSTALL_DIR
- echo "source('http://bioconductor.org/biocLite.R')" > $INSTALL_DIR/runme.R
- echo "installme=c('edgeR','limma','DESeq','DESeq2')" >> $INSTALL_DIR/runme.R
- echo "biocLite()" >> $INSTALL_DIR/runme.R
- echo "biocLite(installme)" >> $INSTALL_DIR/runme.R
- echo "install.packages(c('stringr','gplots'),dependencies=T,repos='http://cran.us.r-project.org')" >> $INSTALL_DIR/runme.R
- echo "quit(save='no')" >> $INSTALL_DIR/runme.R
- export PATH=$PATH && export R_HOME=$R_HOME && export R_LIBS=$R_LIBS && R CMD BATCH $INSTALL_DIR/runme.R
-
-
- Installs some basic bioc packages for the edgeR wrapper and dependencies graphicsmagick (replaces imagemagick) and ghostscript for compressing R's bloated pdfs
- It's clunky but this is the most convenient way I could get anything installed into the package_r3
- Note we use cran at fred hutch since no fastest mirror thingy
-
-
-