For the snps to create combine snps and filtered indels, now using a VCF with just snps instead of vcf with snps plus unfiltered indels.
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@5904 348d0f76-0448-11de-a6fe-93d51630548a
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@ -188,8 +188,8 @@ class WholeGenomePipeline extends QScript {
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val combineSNPsIndels = new CombineVariants with CommandLineGATKArgs
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combineSNPsIndels.rodBind :+= RodBind("indels", "VCF", selectIndels.out)
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combineSNPsIndels.rodBind :+= RodBind("all", "VCF", combineChunks.out)
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combineSNPsIndels.rod_priority_list = "indels,all"
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combineSNPsIndels.rodBind :+= RodBind("snps", "VCF", selectSNPs.out)
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combineSNPsIndels.rod_priority_list = "indels,snps"
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combineSNPsIndels.filteredRecordsMergeType = org.broadinstitute.sting.gatk.contexts.variantcontext.VariantContextUtils.FilteredRecordMergeType.KEEP_IF_ANY_UNFILTERED
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combineSNPsIndels.assumeIdenticalSamples = true
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combineSNPsIndels.out = projectBase + ".unrecalibrated.vcf"
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