view tmap_wrapper_0.3.3/tmap_index.loc.sample @ 2:e2640d81157a default tip

* moving to TMAP 0.3.3

#This is a sample file distributed with Galaxy that enables tools
#to use a directory of TMAP indexed sequences data files. You will need
#to create these data files and then create a tmap_index.loc file
#similar to this one (store it in this directory) that points to
#the directories in which those files are stored. The tmap_index.loc
#file has this format (longer white space characters are TAB characters):
#
#<unique_build_id>   <dbkey>   <display_name>   <file_path>
#
#So, for example, if you had phiX indexed stored in 
#/depot/data2/galaxy/phiX/base/, 
#then the tmap_index.loc entry would look like this:
#
#phiX174   phiX   phiX Pretty   /depot/data2/galaxy/phiX/base/phiX.fa
#
#and your /depot/data2/galaxy/phiX/base/ directory
#would contain phiX.fa.* files:
#
#-rw-r--r--  1 nhomer  staff   5.3K Feb 25 21:19 phi.x.174.fa
#-rw-r--r--  1 nhomer  staff    24B Feb 24 14:50 phi.x.174.fa.fai
#-rw-r--r--  1 nhomer  staff    68B Feb 25 21:19 phi.x.174.fa.tmap.anno
#-rw-r--r--  1 nhomer  staff   1.3M Feb 25 21:19 phi.x.174.fa.tmap.bwt
#-rw-r--r--  1 nhomer  staff   1.3K Feb 25 21:19 phi.x.174.fa.tmap.pac
#-rw-r--r--  1 nhomer  staff   2.6K Feb 25 21:19 phi.x.174.fa.tmap.sa
#...etc...
#
#Your tmap_index.loc file should include an entry per line for each
#index set you have stored. The "file" in the path does not actually
#exist, but it is the prefix for the actual index files.  For example:
#
#phiX174              phiX   phiX174          /depot/data2/galaxy/phiX/base/phiX.fa
#hg18canon            hg18   hg18 Canonical   /depot/data2/galaxy/hg18/base/hg18canon.fa
#hg18full             hg18   hg18 Full        /depot/data2/galaxy/hg18/base/hg18full.fa
#/orig/path/hg19.fa   hg19   hg19             /depot/data2/galaxy/hg19/base/hg19.fa
#...etc...
#
#Note that for backwards compatibility with workflows, the unique ID of
#an entry must be the path that was in the original loc file, because that
#is the value stored in the workflow for that parameter. That is why the
#hg19 entry above looks odd. New genomes can be better-looking.
#