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planemo upload for repository https://github.com/wm75/mimodd_galaxy_wrappers commit 44e872b808f88eacd05963fc2478da2c07b50228
author | wolma |
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date | Thu, 22 Mar 2018 10:32:39 -0400 |
parents | f0f2795de2c7 |
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<tool id="mimodd_covstats" name="MiModD Coverage Statistics" version="@MIMODD_WRAPPER_VERSION@"> <description> calculates coverage statistics for a BCF file as generated by the MiModd Variant Calling tool </description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements" /> <expand macro="stdio" /> <expand macro="version_command" /> <command><![CDATA[ mimodd covstats '$ifile' --ofile '$ofile' ]]></command> <inputs> <param name="ifile" type="data" format="bcf" label="BCF input file" help="Use the Variant Calling tool to generate input for this tool."/> </inputs> <outputs> <data name="ofile" format="tabular" label="Coverage Statistics for ${on_string}"/> </outputs> <tests> <test> <param name="ifile" value="a.bcf" /> <output name="ofile" ftype="tabular"> <assert_contents> <has_n_columns n="3" /> <has_line_matching expression="^chrI	.+" /> <has_line_matching expression="^chrII	.+" /> <has_line_matching expression="^chrIII	.+" /> <has_line_matching expression="^chrIV	.+" /> <has_line_matching expression="^chrV	.+" /> <has_line_matching expression="^chrX	.+" /> <has_line_matching expression="^MtDNA	.+" /> </assert_contents> </output> </test> </tests> <help><![CDATA[ .. class:: infomark **What it does** The tool takes as input a BCF file produced by the *Variant Calling* tool, and calculates per-chromosome read coverage from it. .. class:: warningmark The tool treats genome positions missing from the BCF input as zero coverage, so it is safe to use ONLY with BCF files produced by the *Variant Calling* tool or through other commands that keep the information for all sites. @HELP_FOOTER@ ]]></help> <expand macro="citations" /> </tool>