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flescai
Posts: 26Member ✭
Hi there, I'm running into an issue with my Queue pipeline, with variants called with HaplotypeCaller. Once I get the raw VCF file, I use VariantAnnotator before VQSR: however, no HaplotypeScore annotation is being produced, resulting in a failure of the VariantRecalibrator step where 'HaplotypeScore' was indicated as an annotation.
I tried to correct the issue by indicating to VariantAnnotator to use all annotations
class AnnotationArguments (t: Target) extends VariantAnnotator with UNIVERSAL_GATK_ARGS {
this.reference_sequence = qscript.referenceFile
// Set the memory limit to 7 gigabytes on each command.
this.memoryLimit = 7
this.input_file :+= qscript.bamFile
this.useAllAnnotations
this.D = qscript.dbSNP_b37
}
But I still can't get any output in the annotated VCF of that parameter. Here an example of a variant
AC=5;AF=0.078;AN=64;ActiveRegionSize=179;ClippingRankSum=-0.568;DB;DP=2025;EVENTLENGTH=0;FS=4.139;InbreedingCoeff=-0.0847;MLEAC=5;MLEAF=0.078;MQ=69.98;MQRankSum=-1.428;NVH=1;NumHapAssembly=15;NumHapEval=13;QD=17.20;QDE=17.20;ReadPosRankSum=-1.762;TYPE=SNP;extType=SNP
Any suggestions on what I might be doing wrong?
thanks very much for your help, Francesco
ebanks
Posts: 483 mod
Answers
Hi Francesco,
Our recommendation is that you follow the best practices for variant detection. It looks like you aren't doing that in your pipeline. That being said, you can always use the Variant Annotator to add the Haplotype Score to your VCF records if you really want to do that.
Eric Banks, PhD -- Group Leader, Methods Development, MPG, Broad Institute of Harvard and MIT
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1 • Off Topic Disagree Agree 1Like WTF •Hi Eric, thanks very much, I didn't quite notice the covariates changed in the new best practice to
thanks for flagging it up! before using "this.useAllAnnotations" I used
but 'HaplotypeScore' was not added anyway. is that because of the output of HaplotypeCaller is different?
thanks for your help, Francesco
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0 • Off Topic Disagree Agree Like WTF •In the upcoming release of GATK v2.2 we restored this functionality and so you'll be getting HaplotypeScore again in your variant calls!
Cheers,
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1 • Off Topic Disagree Agree 1Like WTF •