Mercurial > repos > glogobyte > isoread
changeset 6:66cc86c611bb draft
Uploaded
author | glogobyte |
---|---|
date | Fri, 16 Oct 2020 18:58:54 +0000 |
parents | 6633f4447090 |
children | 4f7120a2684e |
files | toolExample_v2.xml |
diffstat | 1 files changed, 136 insertions(+), 0 deletions(-) [+] |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/toolExample_v2.xml Fri Oct 16 18:58:54 2020 +0000 @@ -0,0 +1,136 @@ + +<tool id="fa_gc_content_1" name="IsoRead: miR and isomiR identification and classification" version="0.1.0"> + <description>for each sequence in a file</description> + <requirements> + <requirement type="package" version="1.7">fpdf</requirement> + <requirement type="package" version="0.8">logomaker</requirement> + <requirement type="package" version="0.6.0">plotnine</requirement> + <requirement type="package" version="3.7.4">python</requirement> + <requirement type="package" version="1.17.3">numpy</requirement> + <requirement type="package" version="3.1.2">matplotlib</requirement> + <requirement type="package" version="0.9.0">seaborn</requirement> + <requirement type="package" version="1.0.3">pandas</requirement> + </requirements> + <command> + #set controls=[] + #for $input in $control# + $controls.extend([str($input.element_identifier),str($input)]) + #end for# + #set treateds=[] + #for $input in $treated# + $treateds.extend([str($input.element_identifier),str($input)]) + #end for# + #if $mir_input.database == "1": + #if $f.fil == "1": + #set path=$mir_input.genome1.fields.path + python -W ignore $__tool_directory__/mirbase_ultra_v2.py -con $controls -tre $treateds -analysis $analysis -tool_dir $__tool_directory__ -gen "$path" -f "$mir_input.database" -umis $umis -percentage "-1" -counts "-1" -name1 "$fal1" -name2 "$fal2" + #end if + #if $f.fil == "2": + #set path=$mir_input.genome1.fields.path + python -W ignore $__tool_directory__/mirbase_ultra_v2.py -con $controls -tre $treateds -analysis $analysis -tool_dir $__tool_directory__ -gen "$path" -f "$mir_input.database" -umis $umis -percentage "$f.fil1" -counts "$f.fil2" -name1 "$fal1" -name2 "$fal2" + #end if + #else: + #if $f.fil == "1": + #set path=$mir_input.genome2.fields.value + python -W ignore $__tool_directory__/mirgene_ultra_v2.py -con $controls -tre $treateds -analysis $analysis -tool_dir $__tool_directory__ -gen "$path" -f "$mir_input.database" -umis $umis -percentage "-1" -counts "-1" -name1 "$fal1" -name2 "$fal2" + #end if + #if $f.fil == "2": + #set path=$mir_input.genome2.fields.value + python -W ignore $__tool_directory__/mirgene_ultra_v2.py -con $controls -tre $treateds -analysis $analysis -tool_dir $__tool_directory__ -gen "$path" -f "$mir_input.database" -umis $umis -percentage "$f.fil1" -counts "$f.fil2" -name1 "$fal1" -name2 "$fal2" + #end if + #end if + + </command> + <inputs> + <param name="analysis" type="select" label="Discover miR with templated or/and non-templated isomiRs" help="Choose the category of miRNAs for detection"> + <option value="1" selected="true">Detection of only templated miRNAs</option> + <option value="2">Detection of templated and non-templated miRNAs</option> + </param> + + <conditional name="mir_input"> + <param name="database" type="select" label="Choose Database of miRNAs organisms" help="Choose which database prefer to be used."> + <option value="1" selected="true">MirBase</option> + <option value="2">MirGene</option> + </param> + <when value="1"> + <param name="genome1" type="select" label="Reference miRNAs (organism)" help="If your genome coordinates of interest is not listed, contact the Galaxy team"> + <options from_data_table="n_spiecies" /> + </param> + </when> + <when value="2"> + <param name="genome2" type="select" label="Reference miRNAs (organism)" help="If your genome coordinates of interest is not listed, contact the Galaxy team"> + <options from_data_table="mirgene" /> + </param> + </when> + </conditional> + + + <param name="fal1" type="text" value="FactorLevel" label="Specify a factor level, typical values could be 'tumor', 'normal', 'treated' or 'control'"/> + <param name="control" format="sam" type="data" multiple="True" label="Select BAM files of the factor level samples" /> + <param name="fal2" type="text" value="FactorLevel" label="Specify a factor level, typical values could be 'tumor', 'normal', 'treated' or 'control'"/> + <param name="treated" format="sam" type="data" multiple="True" label="Select BAM files of the factor level samples" /> + + <conditional name="f"> + <param name="fil" type="select" label="Filter low counts" help="Treat genes with very low expression as unexpressed and filter out"> + <option value="1" selected="true">No</option> + <option value="2">Yes</option> + </param> + <when value="2"> + <param name="fil1" type="integer" value="0" label="Minimum percentage of the samples" help="Filter out all genes that do not meet the Minimum counts in at least this many samples of every category"/> + <param name="fil2" type="integer" value="0" label="Minimum counts" help="Filter out all genes that do not meet this minimum count"/> + </when> + <when value="1"> + </when> + </conditional> + + <param name="db" type="boolean" checked="true" truevalue="1" falsevalue="0" label="Output Database files" /> + <param name="cmatrix" type="boolean" checked="false" truevalue="1" falsevalue="0" label="Output Matrix files, one for each factor level" /> + <param name="c_files" type="boolean" checked="true" truevalue="1" falsevalue="0" label="Output Count tables, one for each sample" /> + <param name="umis" type="boolean" checked="false" truevalue="1" falsevalue="0" label="Collapsing sam files if samples include UMIs" /> + </inputs> + <outputs> + <collection name="list_output1" type="list" label="Database ${fal1} templated" > + <discover_datasets pattern="__name__" format="tabular" directory="split1" /> + <filter>db == 1 and (analysis == "1" or analysis == "2")</filter> + </collection> + <collection name="list_output2" type="list" label="Database ${fal2} templated" > + <discover_datasets pattern="__name__" format="tabular" directory="split2" /> + <filter>db == 1 and (analysis == "1" or analysis == "2")</filter> + </collection> + <collection name="list_output3" type="list" label="Database ${fal1} non-templated" > + <discover_datasets pattern="__name__" format="tabular" directory="split3" /> + <filter>db == 1 and analysis == "2"</filter> + </collection> + <collection name="list_output4" type="list" label="Database ${fal2} non-templated" > + <discover_datasets pattern="__name__" format="tabular" directory="split4" /> + <filter>db == 1 and analysis == "2"</filter> + </collection> + + <collection name="Counts" type="list" label="Count Matrices" > + <discover_datasets pattern="__name__" format="tabular" directory="Counts" /> + <filter>cmatrix==1</filter> + </collection> + + + <collection name="list_output9" type="list" label="Count files ${fal1} for Differential Expression" > + <discover_datasets pattern="__name__" format="tabular" directory="Diff/temp_con" /> + <filter>c_files==1 and (analysis == "1")</filter> + </collection> + <collection name="list_output10" type="list" label="Count files ${fal2} for Differential Expression" > + <discover_datasets pattern="__name__" format="tabular" directory="Diff/temp_tre" /> + <filter>c_files==1 and (analysis == "1")</filter> + </collection> + <collection name="list_output11" type="list" label="Count files ${fal1} for Differential Expression" > + <discover_datasets pattern="__name__" format="tabular" directory="Diff/n_temp_con" /> + <filter>c_files==1 and analysis == "2"</filter> + </collection> + <collection name="list_output12" type="list" label="Count files ${fal2} for Differential Expression" > + <discover_datasets pattern="__name__" format="tabular" directory="Diff/n_temp_tre" /> + <filter>c_files==1 and analysis == "2"</filter> + </collection> + + <data name="Results non templated treated1" format="pdf" label="PDF" from_work_dir="$__tool_directory__/report1.pdf" /> + </outputs> + <help> + </help> +</tool>