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1 <?xml version="1.0" ?>
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2
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3 <tool id="generate_genomeid" name='Generate GenomeID' version='1.0.0' hidden='false'>
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4
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5 <command interpreter="perl">
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6 generateID.pl --o $genomeID --n $noise --hg $hg --b $baq --s $sex --u $ucn --r $ref
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7 #if $source.source_select=="bam"
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8 --type bam --file $bamFile
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9 #elif $source.source_select=="vcf"
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10 --type vcf --file $vcfFile
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11 #else
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12 --type tbi --file $tbi_gz
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13 #end if
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14 #if $sampleName
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15 --sN $sampleName
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16 #end if
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17
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18 </command>
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19
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20 <inputs>
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21 <conditional name="source">
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22 <param name="source_select" type="select" label="Sequence Source Type">
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23 <option value="bam">Binary Alignment Map (BAM)</option>
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24 <option value="vcf">Variant Call Format (VCF)</option>
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25 <option value="tbi">Indexed TAB-delimited (TABIX)</option>
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26 </param>
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27
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28 <when value="bam">
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29 <param name="bamFile" type="data" format="bam" label="BAM file" help="If file is not listed, ensure it is set to bam datatype"></param>
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30 </when>
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31
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32 <when value="vcf">
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33 <param name="vcfFile" type="data" format="vcf" label="VCF File" help="If file is not listed, ensure it is set to vcf datatype"></param>
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34 </when>
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35
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36 <when value="tbi">
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37 <param name="tbi_gz" type="data" format="vcf_bgzip" label="Compressed VCF File" help="If file is not listed, ensure it is set to vcf_bgzip datatype"></param>
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38 </when>
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39
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40 </conditional>
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41
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42 <param name="hg" type="select" label="Version of the reference Human Genome" help="Warning: Selection of Unknown may return a poor identifier">
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43 <option value="hg19">Human Genome Version 19</option>
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44 <option value="hg38">Human Genome Version 38</option>
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45 <option value="none">Unknown</option>
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46 </param>
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47
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48 <param name="sampleName" type="text" label="Name of the sample" help="Used if source file contains more than one sample"></param>
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49 <param name="noise" type="float" value="0.05" label="Threshold for maximum allowed noise"></param>
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50 <param name="baq" type="integer" value="30" label=""></param>
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51 <param name="sex" type="boolean" checked="true" label="Include Sex Chromosome Information"></param>
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52 <param name="ucn" type="boolean" checked="false" label="Sample has unusual copy number"></param>
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53 <param name="ref" type="boolean" checked="false" label="Match to reference geneome if marker not found"></param>
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54
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55 </inputs>
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56
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57 <outputs>
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58 <data name="genomeID" format="txt" label="${sampleName}_genomeID" />
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59 </outputs>
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60 </tool>
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