Mercurial > repos > azomics > metacyto_checkpanel
view metacyto_checkpanel.xml @ 0:67d79ba0f7aa draft default tip
"planemo upload for repository https://github.com/ImmPortDB/immport-galaxy-tools/tree/master/flowtools/check_headers commit 14b2e4d834a9856236affb7b77debecca360c542"
author | azomics |
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date | Tue, 27 Jul 2021 21:47:56 +0000 |
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<tool id="metacyto_checkpanel" name="Check markers in analysis panels" version="1.0+galaxy0" profile="18.01"> <description>for MetaCyto</description> <requirements> <requirement type="package" version="1.4.0">bioconductor-metacyto</requirement> </requirements> <stdio> <exit_code range="1:9" /> <exit_code range="10" level="fatal" description="The input file cannot be used. Please check input format." /> <exit_code range="11:" /> </stdio> <command><![CDATA[ Rscript --slave --vanilla '$__tool_directory__/metacyto_checkpanel.R' '${input_file}' '${output_file}'; #if $graph=="TRUE" mv panel_summary.pdf '${pdf_out}' #end if ]]> </command> <inputs> <param format="metacyto_summary.txt" name="input_file" type="data" label="MetaCyto preprocessing summary"/> <param name="graph" type="boolean" label="Output visual summary?" checked="false" truevalue="TRUE" falsevalue="FALSE" /> </inputs> <outputs> <data format="tabular" name="output_file" label="Panel Summary of ${input_file.name}"/> <data format="pdf" name="pdf_out" label="Visual Panel Summary of ${input_file.name}"> <filter>(graph)</filter> </data> </outputs> <tests> <test> <param name="input_file" value="mc_preprocesss_summary.metacyto_summary.txt"/> <param name="graph" value="True"/> <output name="output_file" ftype="tabular"> <assert_contents> <has_n_columns n="3" /> <has_text text="CD95" /> <has_n_lines n="14" /> </assert_contents> </output> <output name="pdf_out" ftype="pdf"> <assert_contents> <has_size value="4569" delta="500" /> </assert_contents> </output> </test> </tests> <help><![CDATA[ Metacyto Check Markers in analysis panels ----------------------------------------- This tool uses MetaCyto's panel summary function to compare marker names between groups of FCS files. **Input** This tool requires the MetaCyto pre-processing Summary as input. **Output** This tool generates a table and an optional visual representation in PDF of how markers are distributed in the FCS file sets. **Example** *Input* - Summary Table:: study_id antibodies filenames group1 Marker1|Marker2|Marker3|... file1.fcs group2 Marker1|Marker2|Marker3|... file2.fcs ... ... ... *Output* - Panel Summary:: Markers group1 group2 ... Marker1 1 1 ... Marker2 1 1 ... Marker3 0 1 ... ... ... ... ... *Graphical output* .. image:: ./images/checkpanel.png ]]> </help> </tool>