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1 <tool id="coverage_stats" name="Coverage Statistics" version="0.1.7.3">
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2 <description>Calculate coverage statistics for a BCF file as generated by the Variant Calling tool</description>
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3 <macros>
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4 <import>toolshed_macros.xml</import>
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5 </macros>
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6 <expand macro="requirements" />
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7 <version_command>mimodd version -q</version_command>
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8 <command>
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9 mimodd covstats "$ifile" --ofile "$output_vcf"
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10 </command>
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11
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12 <inputs>
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13 <param format="bcf" help="Use the Variant Calling tool to generate input for this tool." label="BCF input file" name="ifile" type="data" />
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14 </inputs>
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15 <outputs>
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16 <data format="tabular" label="Coverage Statistics for ${on_string}" name="output_vcf" />
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17 </outputs>
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18
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19 <help>
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20 .. class:: infomark
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21
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22 **What it does**
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23
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24 The tool takes as input a BCF file produced by the *Variant Calling* tool, and calculates per-chromosome read coverage from it.
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25
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26 .. class:: warningmark
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27
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28 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.
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29
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30 </help>
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31 </tool>
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