Expanded target pipeline complete. Stop trying to be clever about scatter-gather; wait until functional SG is built-in to Q. Til then, a lazy version of the fullCallingPipeline. Seems to take a long time to generate the graph though...

git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@4888 348d0f76-0448-11de-a6fe-93d51630548a
This commit is contained in:
chartl 2010-12-21 00:56:16 +00:00
parent 758d14a261
commit 80770dc032
1 changed files with 26 additions and 47 deletions

View File

@ -1,7 +1,6 @@
import org.broadinstitute.sting.commandline.ArgumentCollection
import org.broadinstitute.sting.queue.extensions.gatk._
import org.broadinstitute.sting.queue.library.ipf.ExpandIntervals
import org.broadinstitute.sting.queue.library.ipf.intervals.GroupIntervals
import org.broadinstitute.sting.queue.pipeline.PipelineArgumentCollection
import org.broadinstitute.sting.queue.QScript
import org.broadinstitute.sting.utils.text.XReadLines
@ -15,7 +14,7 @@ class expanded_targets extends QScript {
def script = {
val intervalExpands : List[ExpandIntervals] = (new Range(0,40,1)).toList.map( u => {
new ExpandIntervals(args.projectIntervals,1+5*u,5,new File(System.getProperty("user.dir")+"/"+args.projectName+"_expanded_%d_%d.interval_list".format(1+5*u,6+5*u)),args.projectRef,"TSV","INTERVALS")
new ExpandIntervals(args.projectIntervals,1+5*u,5,new File("./"+args.projectName+"_expanded_%d_%d.interval_list".format(1+5*u,6+5*u)),args.projectRef,"TSV","INTERVALS")
})
trait GATKArgs extends CommandLineGATK {
@ -24,7 +23,7 @@ class expanded_targets extends QScript {
this.jarFile = args.gatkJar
}
val userDir = System.getProperty("user.dir")
val userDir = "."
addAll(intervalExpands)
@ -41,54 +40,22 @@ class expanded_targets extends QScript {
rtc
})
val clean : List[IndelRealigner] = realign.map( u => {
var clean : IndelRealigner = new IndelRealigner with GATKArgs
clean.targetIntervals = u.out
clean.input_file = u.input_file
clean.memoryLimit = Some(4)
clean.out = new File(userDir+"/"+swapExt(u.out,".bam",".expanded.targets.bam").getName)
clean
var cleaner : IndelRealigner = new IndelRealigner with GATKArgs
cleaner.targetIntervals = u.out
cleaner.input_file = u.input_file
cleaner.memoryLimit = Some(4)
cleaner.out = new File(userDir+"/"+swapExt(u.out,".bam",".expanded.targets.bam").getName)
cleaner
})
addAll(realign)
addAll(clean)
val callFiles: List[File] = intervalExpands.map(u => makeCalls(u.outList,20,clean.map(h => h.out)))
val callFiles: List[File] = intervalExpands.map(u => makeCalls(u.outList,clean.map(h => h.out)))
}
def makeCalls(iList: File, scatterNo: Int, bams: List[File]): File = {
var scatters : GroupIntervals = new GroupIntervals(iList,20,true,Some(System.getProperty("user.dir")))
var filtered : List[(File,File)] = scatters.outputList.zipWithIndex.map(v => reallyMakeCalls(v._1,bams,v._2))
var gatherStandard : VcfGatherFunction = new VcfGatherFunction
gatherStandard.gatherParts = filtered.map(u => u._1)
gatherStandard.originalOutput = swapExt(iList,".interval_list",".filtered.calls.vcf")
var gatherHiseq : VcfGatherFunction = new VcfGatherFunction
gatherHiseq.gatherParts = filtered.map(u => u._2)
gatherHiseq.originalOutput = swapExt(iList,".interval_list",".filtered.hiseq.vcf")
add(scatters)
add(gatherStandard)
add(gatherHiseq)
trait GATKArgs extends CommandLineGATK {
this.reference_sequence = args.projectRef
this.DBSNP = args.projectDBSNP
this.jarFile = args.gatkJar
}
var eval : VariantEval = new VariantEval with GATKArgs
eval.rodBind :+= new RodBind("evalInterval","vcf",gatherStandard.originalOutput)
eval.rodBind :+= new RodBind("compHiSeq","vcf",new File("/humgen/gsa-hpprojects/GATK/data/Comparisons/Unvalidated/NA12878/NA12878.hg19.HiSeq.WGS.cleaned.ug.snpfiltered.indelfiltered.optimized.cut.vcf"))
eval.rodBind :+= new RodBind("compHiSeq_atSites","vcf",gatherHiseq.originalOutput)
eval.rodBind :+= new RodBind("compOMNI","vcf",new File("/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/Omni2.5_chip/Omni_2.5_764_samples.b37.deduped.annot.vcf"))
eval.out = swapExt(iList,".interval_list",".eval")
eval.reportType = Option(org.broadinstitute.sting.utils.report.VE2ReportFactory.VE2TemplateType.CSV)
eval.out
}
def reallyMakeCalls(iList: File, bams : List[File], scatterNo: Int) : (File,File) = {
def makeCalls(iList: File, bams: List[File]): File = {
trait GATKArgs extends CommandLineGATK {
this.reference_sequence = args.projectRef
@ -99,25 +66,37 @@ class expanded_targets extends QScript {
var call : UnifiedGenotyper = new UnifiedGenotyper with GATKArgs
call.input_file = bams
call.out = swapExt(iList,".interval_list",".scatter%d.raw.vcf".format(scatterNo))
call.out = swapExt(iList,".interval_list",".raw.vcf")
call.trig_emit_conf = Some(0.0)
call.rodBind :+= new RodBind("trigger","vcf",thisTrigger)
call.scatterCount = 10
call.memoryLimit = Some(6)
var filter : VariantFiltration = new VariantFiltration with GATKArgs
filter.rodBind :+= new RodBind("variant","vcf",call.out)
filter.filterExpression :+= "\"QD<5.0\""
filter.filterName :+= "LowQualByDepth"
filter.filterExpression :+= "\"SB>-0.10\""
filter.filterName :+= "HighStrandBias"
filter.out = swapExt(iList,".interval_list",".scatter%d.filtered.vcf".format(scatterNo))
filter.out = swapExt(iList,".interval_list",".filtered.vcf")
var callHiseq : UnifiedGenotyper = new UnifiedGenotyper with GATKArgs
callHiseq.input_file = List(new File("/humgen/1kg/analysis/bamsForDataProcessingPapers/NA12878.HiSeq.WGS.bwa.cleaned.recal.bam"))
callHiseq.rodBind :+= new RodBind("trigger","vcf",filter.out)
callHiseq.out = swapExt(iList,".interval_list",".scatter%d.hiSeq.genotypes.vcf".format(scatterNo))
callHiseq.out = swapExt(iList,".interval_list",".hiSeq.genotypes.vcf")
callHiseq.trig_emit_conf = Some(0.0)
callHiseq.scatterCount = 5
add(call,filter,callHiseq)
return (filter.out,callHiseq.out)
var eval : VariantEval = new VariantEval with GATKArgs
eval.rodBind :+= new RodBind("evalInterval","vcf",filter.out)
eval.rodBind :+= new RodBind("compHiSeq","vcf",new File("/humgen/gsa-hpprojects/GATK/data/Comparisons/Unvalidated/NA12878/NA12878.hg19.HiSeq.WGS.cleaned.ug.snpfiltered.indelfiltered.optimized.cut.vcf"))
eval.rodBind :+= new RodBind("compHiSeq_atSites","vcf",callHiseq.out)
eval.rodBind :+= new RodBind("compOMNI","vcf",new File("/humgen/gsa-hpprojects/GATK/data/Comparisons/Validated/Omni2.5_chip/Omni_2.5_764_samples.b37.deduped.annot.vcf"))
eval.out = swapExt(iList,".interval_list",".eval")
eval.reportType = Option(org.broadinstitute.sting.utils.report.VE2ReportFactory.VE2TemplateType.CSV)
add(eval)
eval.out
}
}