annotate vcfToMutationVector.xml @ 7:1d150e860c4d

Expanded the functionality of the merge genomic datasets tool, to generate an output dataset with the file (or label) indicating where each column came from
author melissacline
date Mon, 09 Mar 2015 19:58:03 -0700
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1 <tool id="vcfToMutationVector" description="Convert SNP output VCF to Xena mutation input format" name="SnpEff VCF To Mutation Vector" version="0.0.1">
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2 <description>
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3 Given a VCF generated by snpEff, generate mutation data for input to Xena
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4 </description>
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5 <command interpreter="python">
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6 vcfToMutationVector.py $inputVcf --trinity $isTrinity > $mutationVector
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7 </command>
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8 <inputs>
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9 <param name="inputVcf" format="tabular" type="data" label="snpEff Output VCF"/>
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10 <param name="isTrinity" type="boolean" truevalue="1" falsevalue="0">
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11 <label>Was the input VCF produced from Trinity output?</label>
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12 </param>
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13 </inputs>
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14 <outputs>
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15 <data name="mutationVector" format="tabular"/>
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16 </outputs>
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17 <help>
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18 This tool will take a VCF file generated by snpEff and format it appropriately for input
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19 to Xena.
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20 </help>
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21 </tool>