Mercurial > repos > wolma > mimodd
comparison covstats.xml @ 0:6231ae8f87b8
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author | wolma |
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date | Wed, 11 Feb 2015 08:29:02 -0500 |
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children | a548b3c6ed00 |
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1 <tool id="coverage_stats" name="Coverage Statistics"> | |
2 <description>Calculate coverage statistics for a BCF file as generated by the Variant Calling tool</description> | |
3 <version_command>mimodd version -q</version_command> | |
4 <command> | |
5 mimodd covstats "$ifile" --ofile "$output_vcf" | |
6 </command> | |
7 | |
8 <inputs> | |
9 <param name="ifile" type="data" format="bcf" label="BCF input file" help="Use the Variant Calling tool to generate input for this tool."/> | |
10 </inputs> | |
11 <outputs> | |
12 <data name="output_vcf" format="tabular" label="Coverage Statistics for ${on_string}"/> | |
13 </outputs> | |
14 | |
15 <help> | |
16 .. class:: infomark | |
17 | |
18 **What it does** | |
19 | |
20 The tool takes as input a BCF file produced by the *Variant Calling* tool, and calculates per-chromosome read coverage from it. | |
21 | |
22 .. class:: warningmark | |
23 | |
24 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. | |
25 | |
26 </help> | |
27 </tool> |