Mercurial > repos > morinlab > strelka
diff strelka.xml @ 2:3ce78c04c7e5 draft
planemo upload for repository https://github.com/morinlab/tools-morinlab/tree/master/tools/strelka commit 4ef2d91b7c1686a2696b92fe538d4aec51d05e40-dirty
| author | morinlab |
|---|---|
| date | Tue, 11 Oct 2016 14:34:44 -0400 |
| parents | 9c9f2706c5e1 |
| children | 4e6e20c9738b |
line wrap: on
line diff
--- a/strelka.xml Thu Aug 18 19:42:43 2016 -0400 +++ b/strelka.xml Tue Oct 11 14:34:44 2016 -0400 @@ -4,123 +4,125 @@ </description> <macros> <import>citations.xml</import> - </macros> + </macros> <requirements> - <requirement type="package" version="1.0.14">strelka</requirement> - <requirement type="set_environment">STRELKA_INSTALL_DIR</requirement> - <requirement type="set_environment">STRELKA_REPOSITORY_DIR</requirement> + <requirement type="package" version="1.0.14">strelka</requirement> </requirements> <command detect_errors="aggressive"> - <!-- LINK BAM INDEX --> ln -s $normal normal.bam; ln -s $normal.metadata.bam_index normal.bam.bai; ln -s $tumour tumour.bam; ln -s $tumour.metadata.bam_index tumour.bam.bai; - - <!-- CREATE CONFIG FILE --> + touch config.ini; - #if #depthfilters == "genome": + echo "[user]" > config.ini; + #if $depthfilters.seqType == "genome": echo "isSkipDepthFilters = 0" >> config.ini; echo "maxInputDepth = 10000" >> config.ini; echo "depthFilterMultiple = 3.0" >> config.ini; - #elif #depthfilters == "exome": + #elif $depthfilters.seqType == "exome": echo "isSkipDepthFilters = 1" >> config.ini; echo "maxInputDepth = 10000" >> config.ini; echo "depthFilterMultiple = 3.0" >> config.ini; - #elif #depthfilters == "targeted": + #elif $depthfilters.seqType == "targeted": echo "isSkipDepthFilters = 1" >> config.ini; echo "maxInputDepth = 10000" >> config.ini; echo "depthFilterMultiple = 3.0" >> config.ini; #else: - echo "isSkipDepthFilters = "$isSkipDepthFilters >> config.ini; - echo "maxInputDepth = "$maxInputDepth >> config.ini; - echo "depthFilterMultiple = "$depthFilterMultiple >> config.ini; + echo "isSkipDepthFilters = " $depthfilters.isSkipDepthFilters >> config.ini; + echo "maxInputDepth = " $depthfilters.maxInputDepth >> config.ini; + echo "depthFilterMultiple = " $depthfilters.depthFilterMultiple >> config.ini; #end if - echo "snvMaxFilteredBasecallFrac = "$advancedsettings.snvMaxFilteredBasecallFrac >> config.ini; - echo "snvMaxSpanningDeletionFrac = "$advancedsettings.snvMaxSpanningDeletionFrac >> config.ini; - echo "indelMaxRefRepeat = "$advancedsettings.indelMaxRefRepeat >> config.ini; - echo "indelMaxWindowFilteredBasecallFrac = "$advancedsettings.indelMaxWindowFilteredBasecallFrac >> config.ini; - echo "indelMaxIntHpolLength = "$advancedsettings.indelMaxIntHpolLength >> config.ini; - echo "ssnvPrior = "$advancedsettings.ssnvPrior >> config.ini; - echo "sindelPrior = "$advancedsettings.sindelPrior >> config.ini; - echo "ssnvNoise = "$advancedsettings.ssnvNoise >> config.ini; - echo "sindelNoise = "$advancedsettings.sindelNoise >> config.ini; - echo "ssnvNoiseStrandBiasFrac = "$advancedsettings.ssnvNoiseStrandBiasFrac >> config.ini; - echo "minTier1Mapq = "$advancedsettings.minTier1Mapq >> config.ini; - echo "minTier2Mapq = "$advancedsettings.minTier2Mapq >> config.ini; - echo "ssnvQuality_LowerBound = "$advancedsettings.ssnvQuality_LowerBound >> config.ini; - echo "sindelQuality_LowerBound = "$advancedsettings.sindelQuality_LowerBound >> config.ini; + + echo "snvMaxFilteredBasecallFrac = " $advancedsettings.snvMaxFilteredBasecallFrac >> config.ini; + echo "snvMaxSpanningDeletionFrac = " $advancedsettings.snvMaxSpanningDeletionFrac >> config.ini; + echo "indelMaxRefRepeat = " $advancedsettings.indelMaxRefRepeat >> config.ini; + echo "indelMaxWindowFilteredBasecallFrac = " $advancedsettings.indelMaxWindowFilteredBasecallFrac >> config.ini; + echo "indelMaxIntHpolLength = " $advancedsettings.indelMaxIntHpolLength >> config.ini; + echo "ssnvPrior = " $advancedsettings.ssnvPrior >> config.ini; + echo "sindelPrior = " $advancedsettings.sindelPrior >> config.ini; + echo "ssnvNoise = " $advancedsettings.ssnvNoise >> config.ini; + echo "sindelNoise = " $advancedsettings.sindelNoise >> config.ini; + echo "ssnvNoiseStrandBiasFrac = " $advancedsettings.ssnvNoiseStrandBiasFrac >> config.ini; + echo "minTier1Mapq = " $advancedsettings.minTier1Mapq >> config.ini; + echo "minTier2Mapq = " $advancedsettings.minTier2Mapq >> config.ini; + echo "ssnvQuality_LowerBound = " $advancedsettings.ssnvQuality_LowerBound >> config.ini; + echo "sindelQuality_LowerBound = " $advancedsettings.sindelQuality_LowerBound >> config.ini; echo "isWriteRealignedBam = 0" >> config.ini; echo "binSize = 25000000" >> config.ini; echo "extraStrelkaArguments = " >> config.ini; - <!-- INDEX GENOME IF HISTORY --> - #if $reference_source == "history": + cat config.ini > $config; + + #if $reference_source.reference_source_selector == "history": ln -s $reference_source.ref_file ref.fa; samtools faidx ref.fa; #end if - <!-- CREATE ORIGINAL STRELKA MAKEFILE --> - \$STRELKA_INSTALL_DIR/bin/configureStrelkaWorkflow.pl + \${STRELKA_INSTALL_DIR}/bin/configureStrelkaWorkflow.pl --normal \$(pwd)/normal.bam --tumor \$(pwd)/tumour.bam - #if $reference_source == "history": - --ref ref.fa + + #if $reference_source.reference_source_selector == "history": + --ref \$(pwd)/ref.fa #else: --ref ${reference_source.ref_file.fields.path} #end if - --config \$(pwd)/config.ini + + --config \$(pwd)/config.ini; #if $interval_file + + cp ./strelkaAnalysis/Makefile ./; + + for int in \$( cat $interval_file ); do - <!-- CREATE SUB-MAKEFILE IF PARALLELISM TURNED ON --> - cp ./strelkaAnalysis/Makefile ./; - - \$REPOSITORY_STRELKA_DIR/parse_strelka_makefile.py + python $__tool_directory__/parse_strelka_makefile.py --makefile Makefile - --chrom \$(cat $interval_file | cut -f1) + --chrom \$int --output ./strelkaAnalysis/Makefile; #end if - <!-- RUN STRELKA --> cd strelkaAnalysis; make -j \${GALAXY_SLOTS:-1}; + cd ../; #if $interval_file - <!-- OUTPUT FOR PARALLEL OPTION - TO BE MERGED --> - cat ./chromosomes/\$(cat $interval_file | cut -f1)/all.somatic.snvs.vcf > $snvs; - cat ./chromosomes/\$(cat $interval_file | cut -f1)/all.somatic.indels.vcf > $indels; - + cat ./strelkaAnalysis/chromosomes/\$int/somatic.snvs.vcf | grep -v "^#.*" >> $snvs; + cat ./strelkaAnalysis/chromosomes/\$int/somatic.indels.vcf | grep -v "^#.*" >> $indels; + + done; + #else - <!-- OUTPUT FOR NORMAL OPTION - ALREADY MERGED --> - cat ./results/all.somatic.snvs.vcf > $snvs; - cat ./results/all.somatic.indels.vcf > $indels; + cat ./strelkaAnalysis/results/all.somatic.snvs.vcf > $snvs; + cat ./strelkaAnalysis/results/all.somatic.indels.vcf > $indels; #end if + </command> <inputs> - <conditional name="reference_source"> + <conditional name="reference_source"> <param label="Choose the source for the reference genome" name="reference_source_selector" type="select"> <option value="cached">Use a built-in genome</option> <option value="history">Use a genome from the history</option> </param> <when value="cached"> - <param label="Reference Genome File" name="ref_file" type="select" > - <options from_data_table="fasta_indexes" /> + <param label="Genome" name="ref_file" type="select"> + <options from_data_table="fasta_indexes"/> </param> </when> <when value="history"> - <param label="Reference Genome File" name="ref_file" type="data" format="fasta" /> + <param label="Genome" name="ref_file" type="data" format="fasta"/> </when> </conditional> - <param type="data" format="bam" name="normal" label="Normal Alignment File" /> - <param type="data" format="bam" name="tumour" label="Tumour Alignment File" /> - <param type="data" format="txt" optional="true" name="interval_file" label="Chromosomes" help="Restrict SNV calls to the following list of chromosomes (one per line)" /> - <conditional type="depthfilters"> + <param type="data" format="bam" name="normal" label="Normal Alignment File"/> + <param type="data" format="bam" name="tumour" label="Tumour Alignment File"/> + <param type="data" format="txt" optional="true" name="interval_file" label="Inteval file" help="Created by make parallel, only use when parallelism is turned on"/> + <conditional name="depthfilters"> <param type="select" name="seqType" label="What Type of Sequencing?"> <option value="genome" selected="true">Whole Genome</option> <option value="exome">Exome</option> @@ -133,7 +135,7 @@ <param name="maxInputDepth" type="integer" label="Max Input Depth" value="10000" help="The upper bound on input depth to load into memory. This filter should not occur with Deep Targeted Sequencing but should occur with Exome or Whole Genome Sequencing. Set to 0 to turn off" min="0"/> </when> </conditional> - <section name="advancedsettings" title="Advanced Settings" expanded="False"> + <section name="advancedsettings" title="Advanced Settings" expanded="false"> <param type="float" name="snvMaxFilteredBasecallFrac" value="0.4" label="SNV Max Filtered Basecall Fraction" help="Filter SNV calls when greater than this fraction of basecalls have been removed by a mismatch density filter in either sample."/> <param type="float" name="snvMaxSpanningDeletionFrac" value="0.75" label="SNV Max Spanning Deletion Fraction" help="Filter SNV calls at sites where greater than this fraction of overlapping reads contain deletions which span the SNV call site."/> <param type="integer" name="indelMaxRefRepeat" value="8" label="Indel Max Reference Homopolymer Length" help="Filter Indel calls if they represent an expansion or contraction of a repeated pattern with a repeat count greater than this value in the reference."/> @@ -151,17 +153,19 @@ </section> </inputs> <outputs> - <data format="vcf" name="snvs" label="Strelka SNVs"/> - <data format="vcf" name="indels" label="Strelka indels"/> + <data format="vcf" name="snvs"/> + <data format="vcf" name="indels"/> + <data format="txt" name="config" /> </outputs> <tests> <test> <param name="normal" value="test.normal.bam"/> - <param name="tumour" value="test.tumour.bam"/> - <param name="reference_source" value="history"/> - <param name="ref_file" value="test.fa"/> - <output name="snvs" ftype="vcf" file="somatic.all.somatic.snvs.vcf" lines_diff="2"/> - <output name="indels" ftype="vcf" file="somatic.all.somatic.indels.vcf" lines_diff="2"/> + <param name="normal.metadata.bam_index" value="test.normal.bam.bai"/> + <param name="tumour" value="test.tumour.bam"/> + <param name="tumour.metadata.bam_index" value="test.tumour.bam.bai"/> + <param name="reference_source.reference_source_selector" value="history"/> + <param name="reference_source.ref_file" value="test.fa"/> + <output name="snvs" ftype="vcf" file="all.somatic.snvs.vcf" lines_diff="2"/> </test> </tests> <help>
