removing the tech dev pipeline script from the repository to keep the methods development pipeline as the reference script.
git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@4992 348d0f76-0448-11de-a6fe-93d51630548a
This commit is contained in:
carneiro
parent
b107c97c1a
commit
c4f9b262e5
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import org.broadinstitute.sting.queue.extensions.gatk._
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import org.broadinstitute.sting.queue.QScript
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//import org.broadinstitute.sting.queue.extensions.picard.PicardBamJarFunction
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//import org.broadinstitute.sting.queue.extensions.samtools.SamtoolsIndexFunction
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//import org.apache.commons.io.FilenameUtils;
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class tdPipeline extends QScript {
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qscript =>
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@Argument(shortName="gatk", doc="gatk jar file", required=true)
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var gatkJarFile: File = _
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@Argument(shortName="outputDir", doc="output directory", required=true)
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var outputDir: String = "./"
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@Argument(shortName="noBAQ", doc="turns off BAQ calculation", required=false)
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var noBAQ: Boolean = false
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@Argument(shortName="noMask", doc="turns off MASK calculation", required=false)
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var noMask: Boolean = false
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trait UNIVERSAL_GATK_ARGS extends CommandLineGATK { logging_level = "INFO"; jarFile = gatkJarFile; memoryLimit = Some(4);}
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class Target(
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val baseName: String,
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val reference: File,
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val dbsnpFile: String,
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val hapmapFile: String,
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val maskFile: String,
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val bamList: File,
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val goldStandard_VCF: File,
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val intervals: String,
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val titvTarget: Double,
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val isLowpass: Boolean) {
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val name = qscript.outputDir + baseName
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val clusterFile = new File(name + ".clusters")
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val rawVCF = new File(name + ".raw.vcf")
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val filteredVCF = new File(name + ".filtered.vcf")
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val titvRecalibratedVCF = new File(name + ".titv.recalibrated.vcf")
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val tsRecalibratedVCF = new File(name + ".ts.recalibrated.vcf")
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val goldStandardName = qscript.outputDir + "goldStandard/" + baseName
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val goldStandardClusterFile = new File(goldStandardName + ".clusters")
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}
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val hg18 = new File("/seq/references/Homo_sapiens_assembly18/v0/Homo_sapiens_assembly18.fasta")
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val b36 = new File("/humgen/1kg/reference/human_b36_both.fasta")
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val b37 = new File("/humgen/1kg/reference/human_g1k_v37.fasta")
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// Define the target datasets here
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val lowPass: Boolean = true
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val HiSeq = new Target("NA12878.HiSeq",
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hg18,
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/dbSNP/dbsnp_129_hg18.rod",
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/HapMap/3.3/genotypes_r27_nr.hg18_fwd.vcf",
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"/humgen/gsa-hpprojects/dev/depristo/oneOffProjects/1000GenomesProcessingPaper/wgs.v13/HiSeq.WGS.cleaned.indels.10.mask",
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new File("/humgen/gsa-hpprojects/NA12878Collection/bams/NA12878.HiSeq.WGS.bwa.cleaned.recal.bam"),
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new File("/home/radon01/depristo/work/oneOffProjects/1000GenomesProcessingPaper/wgs.v13/HiSeq.WGS.cleaned.ug.snpfiltered.indelfiltered.vcf"),
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"/humgen/1kg/processing/pipeline_test_bams/whole_genome_chunked.hg18.intervals",
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2.07,
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!lowPass)
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val FIN = new Target("FIN",
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b37,
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/dbSNP/dbsnp_132_b37.leftAligned.vcf",
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/HapMap/3.3/genotypes_r27_nr.b37_fwd.vcf",
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"/humgen/1kg/processing/pipeline_test_bams/pilot1.dindel.mask.b37.bed",
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new File("/humgen/1kg/processing/pipeline_test_bams/FIN.79sample.Nov2010.chr20.bam"),
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new File("/humgen/gsa-hpprojects/dev/data/AugChr20Calls_v4_3state/ALL.august.v4.chr20.filtered.vcf"), // ** THIS GOLD STANDARD NEEDS TO BE CORRECTED **
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"/humgen/1kg/processing/pipeline_test_bams/whole_genome_chunked.chr20.hg19.intervals",
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2.3,
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lowPass)
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val WEx = new Target("NA12878.WEx",
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hg18,
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/dbSNP/dbsnp_129_hg18.rod",
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/HapMap/3.3/genotypes_r27_nr.hg18_fwd.vcf",
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"/humgen/gsa-hpprojects/dev/depristo/oneOffProjects/1000GenomesProcessingPaper/wgs.v13/GA2.WEx.cleaned.indels.10.mask",
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new File("/humgen/gsa-hpprojects/NA12878Collection/bams/NA12878.WEx.cleaned.recal.bam"),
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new File("/home/radon01/depristo/work/oneOffProjects/1000GenomesProcessingPaper/wgs.v13/GA2.WEx.cleaned.ug.snpfiltered.indelfiltered.vcf"),
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"/seq/references/HybSelOligos/whole_exome_agilent_1.1_refseq_plus_3_boosters/whole_exome_agilent_1.1_refseq_plus_3_boosters.targets.interval_list",
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2.6,
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!lowPass)
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val WEx1kg = new Target("1000G.WEx.GdA",
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b37,
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/dbSNP/dbsnp_132_b37.leftAligned.vcf",
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/HapMap/3.3/genotypes_r27_nr.b37_fwd.vcf",
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"/humgen/1kg/processing/pipeline_test_bams/pilot1.dindel.mask.b37.bed",
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new File("/humgen/1kg/processing/pipeline_test_bams/Barcoded_1000G_WEx_Reduced_Plate_1.cleaned.list"), // BUGBUG: reduce from 60 to 20 people
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new File("/humgen/gsa-scr1/delangel/NewUG/calls/AugustRelease.filtered_Q50_QD5.0_SB0.0.allSamples.SNPs_hg19.WEx_UG_newUG_MQC.vcf"), // ** THIS GOLD STANDARD NEEDS TO BE CORRECTED **
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"/seq/references/HybSelOligos/whole_exome_agilent_1.1_refseq_plus_3_boosters/whole_exome_agilent_1.1_refseq_plus_3_boosters.Homo_sapiens_assembly19.targets.interval_list",
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2.6,
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!lowPass)
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/*
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// Needs an interval file, and a decent TiTv estimate.
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val PacBio = new Target("pacbio",
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b37,
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/dbSNP/dbsnp_132_b37.leftAligned.vcf",
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"/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/HapMap/3.3/genotypes_r27_nr.b37_fwd.vcf",
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"/humgen/1kg/processing/pipeline_test_bams/pilot1.dindel.mask.b37.bed",
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new File("/humgen/gsa-scr1/carneiro/prj/pacbio/pb_reads.18.recal.bam"),
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new File("/humgen/gsa-scr1/carneiro/prj/pacbio/pb_reads.18.recal.bam"),
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"",
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2.00,
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!lowPass
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)
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*/
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/*
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* These sources need to be updated, never used.
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val LowPassN60 = new Target("lowpass.N60", b36, "b36", // which reference the data is aligned to
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new File("/humgen/1kg/analysis/bamsForDataProcessingPapers/lowpass_b36/lowpass.chr20.cleaned.matefixed.bam"), // the bam list to call from
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new File("/home/radon01/depristo/work/oneOffProjects/VQSRCutByNRS/lowpass.N60.chr20.filtered.vcf"), // the gold standard VCF file to run through the VQSR
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"/humgen/1kg/processing/pipeline_test_bams/whole_genome_chunked.chr20.b36.intervals", 2.3, lowPass) // chunked interval list to use with Queue's scatter/gather functionality
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val LowPassAugust = new Target("ALL.august.v4", b37, "b37", // BUGBUG: kill this, it is too large
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new File("/humgen/1kg/processing/allPopulations_chr20_august_release.cleaned.merged.bams/ALL.cleaned.merged.list"),
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new File("/humgen/gsa-hpprojects/dev/data/AugChr20Calls_v4_3state/ALL.august.v4.chr20.filtered.vcf"),
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"/humgen/1kg/processing/pipeline_test_bams/whole_genome_chunked.chr20.hg19.intervals", 2.3, lowPass)
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val LowPassEUR363Nov = new Target("EUR.nov2010", b37, "b37",
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new File("/humgen/1kg/processing/pipeline_test_bams/EUR.363sample.Nov2010.chr20.bam"),
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new File("/humgen/gsa-hpprojects/dev/data/AugChr20Calls_v4_3state/ALL.august.v4.chr20.filtered.vcf"), // ** THIS GOLD STANDARD NEEDS TO BE CORRECTED **
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"/humgen/1kg/processing/pipeline_test_bams/whole_genome_chunked.chr20.hg19.intervals", 2.3, lowPass)
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*/
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val targets = List(HiSeq)
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def script = {
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val goldStandard = true
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for (target <- targets) {
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add(new UnifiedGenotyper(target))
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add(new VariantFiltration(target))
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add(new GenerateVariantClusters(target, !goldStandard))
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add(new VariantRecalibratorTiTv(target, !goldStandard))
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add(new VariantRecalibratorNRS(target, !goldStandard))
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add(new VariantEvaluation(target))
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}
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}
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val FiltersToIgnore = List("DPFilter", "ABFilter", "ESPStandard", "QualByDepth", "StrandBias", "HomopolymerRun")
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// 1.) Call SNPs with UG
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class UnifiedGenotyper(t: Target) extends org.broadinstitute.sting.queue.extensions.gatk.UnifiedGenotyper with UNIVERSAL_GATK_ARGS {
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this.reference_sequence = t.reference
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if (t.dbsnpFile.endsWith(".rod")) this.DBSNP = new File(t.dbsnpFile)
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else if (t.dbsnpFile.endsWith(".vcf")) this.rodBind :+= RodBind("dbsnp", "VCF", t.dbsnpFile)
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this.intervalsString ++= List(t.intervals)
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this.scatterCount = 63 // the smallest interval list has 63 intervals, one for each Mb on chr20
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this.dcov = Some( if ( t.isLowpass ) { 50 } else { 250 } )
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this.input_file :+= t.bamList
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this.out = t.rawVCF
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this.baq = Some( if (noBAQ) {org.broadinstitute.sting.utils.baq.BAQ.CalculationMode.OFF} else {org.broadinstitute.sting.utils.baq.BAQ.CalculationMode.RECALCULATE})
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this.stand_call_conf = Some( if ( t.isLowpass ) { 4.0 } else { 30.0 } )
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this.stand_emit_conf = Some( if ( t.isLowpass ) { 4.0 } else { 30.0 } )
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this.analysisName = t.name + "_UG"
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}
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// 2.) Filter SNPs
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class VariantFiltration(t: Target) extends org.broadinstitute.sting.queue.extensions.gatk.VariantFiltration with UNIVERSAL_GATK_ARGS {
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this.reference_sequence = t.reference
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this.intervalsString ++= List(t.intervals)
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this.scatterCount = 10
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this.variantVCF = t.rawVCF
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this.out = t.filteredVCF
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if (!noMask) {
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this.rodBind :+= RodBind("mask", "Bed", t.maskFile)
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this.maskName = "InDel"
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}
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this.filterName ++= List("HARD_TO_VALIDATE")
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this.filterExpression ++= List("\"MQ0 >= 4 && (MQ0 / (1.0 * DP)) > 0.1\"")
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this.analysisName = t.name + "_VF"
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}
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// 3.) VQSR part1 Generate Gaussian clusters based on truth sites
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class GenerateVariantClusters(t: Target, goldStandard: Boolean) extends org.broadinstitute.sting.queue.extensions.gatk.GenerateVariantClusters with UNIVERSAL_GATK_ARGS {
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val name: String = if ( goldStandard ) { t.goldStandardName } else { t.name }
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this.reference_sequence = t.reference
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if (t.dbsnpFile.endsWith(".rod")) this.DBSNP = new File(t.dbsnpFile)
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else if (t.dbsnpFile.endsWith(".vcf")) this.rodBind :+= RodBind("dbsnp", "VCF", t.dbsnpFile)
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this.rodBind :+= RodBind("hapmap", "VCF", t.hapmapFile)
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this.rodBind :+= RodBind("input", "VCF", if ( goldStandard ) { t.goldStandard_VCF } else { t.filteredVCF } )
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this.clusterFile = if ( goldStandard ) { t.goldStandardClusterFile } else { t.clusterFile }
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this.use_annotation ++= List("QD", "SB", "HaplotypeScore", "HRun")
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this.analysisName = name + "_GVC"
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this.intervalsString ++= List(t.intervals)
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this.qual = Some(300) // clustering parameters to be updated soon pending new experimentation results
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this.std = Some(3.5)
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this.mG = Some(16)
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this.ignoreFilter ++= FiltersToIgnore
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}
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// 4.) VQSR part2 Calculate new LOD for all input SNPs by evaluating the Gaussian clusters
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class VariantRecalibratorBase(t: Target, goldStandard: Boolean) extends org.broadinstitute.sting.queue.extensions.gatk.VariantRecalibrator with UNIVERSAL_GATK_ARGS {
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val name: String = if ( goldStandard ) { t.goldStandardName } else { t.name }
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this.reference_sequence = t.reference
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if (t.dbsnpFile.endsWith(".rod")) this.DBSNP = new File(t.dbsnpFile)
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else if (t.dbsnpFile.endsWith(".vcf")) this.rodBind :+= RodBind("dbsnp", "VCF", t.dbsnpFile)
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this.rodBind :+= RodBind("hapmap", "VCF", t.hapmapFile)
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this.rodBind :+= RodBind("truth", "VCF", t.hapmapFile)
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this.rodBind :+= RodBind("input", "VCF", if ( goldStandard ) { t.goldStandard_VCF } else { t.filteredVCF } )
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this.clusterFile = if ( goldStandard ) { t.goldStandardClusterFile } else { t.clusterFile }
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this.analysisName = name + "_VR"
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this.intervalsString ++= List(t.intervals)
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this.ignoreFilter ++= FiltersToIgnore
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this.ignoreFilter ++= List("HARD_TO_VALIDATE")
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this.priorDBSNP = Some(2.0)
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this.priorHapMap = Some(2.0)
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this.target_titv = t.titvTarget
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}
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// 4a.) Choose VQSR tranches based on novel ti/tv
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class VariantRecalibratorTiTv(t: Target, goldStandard: Boolean) extends VariantRecalibratorBase(t, goldStandard) {
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this.tranche ++= List("0.1", "1.0", "10.0", "100.0")
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this.out = new File(this.name + ".titv.recalibrated.vcf")
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this.tranchesFile = new File(this.name + ".titv.tranches")
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}
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// 4b.) Choose VQSR tranches based on sensitivity to truth set
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class VariantRecalibratorNRS(t: Target, goldStandard: Boolean) extends VariantRecalibratorBase(t, goldStandard) {
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this.sm = Some(org.broadinstitute.sting.gatk.walkers.variantrecalibration.VariantRecalibrator.SelectionMetricType.TRUTH_SENSITIVITY)
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this.tranche ++= List("0.1", "1.0", "10.0", "100.0")
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this.out = new File(this.name + ".ts.recalibrated.vcf")
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this.tranchesFile = new File(this.name + ".ts.tranches")
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}
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// 5.) Variant Evaluation generates the csv files for Genome Concordance analysis
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class VariantEvaluation(t: Target) extends org.broadinstitute.sting.queue.extensions.gatk.VariantEval with UNIVERSAL_GATK_ARGS {
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val name: String = t.name
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this.reference_sequence = t.reference
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if (t.dbsnpFile.endsWith(".rod")) this.DBSNP = new File(t.dbsnpFile)
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else if (t.dbsnpFile.endsWith(".vcf")) this.rodBind :+= RodBind("dbsnp", "VCF", t.dbsnpFile)
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this.rodBind :+= RodBind("hapmap", "VCF", t.hapmapFile)
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this.rodBind :+= RodBind("eval", "VCF", t.tsRecalibratedVCF)
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this.analysisName = name + "_VR"
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this.intervalsString ++= List(t.intervals)
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this.reportType = Some(org.broadinstitute.sting.utils.report.VE2ReportFactory.VE2TemplateType.R)
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this.reportLocation = new File(t.name + ".eval")
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this.noStandard = true
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this.evalModule ++= List("TiTvVariantEvaluator", "CountVariants", "GenotypeConcordance")
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}
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}
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