Possible fix for reduced reads coming from the HaplotypeCaller in the AD
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@ -13,6 +13,7 @@ import org.broadinstitute.sting.utils.codecs.vcf.VCFStandardHeaderLines;
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import org.broadinstitute.sting.utils.pileup.PileupElement;
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import org.broadinstitute.sting.utils.pileup.ReadBackedPileup;
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import org.broadinstitute.sting.utils.sam.GATKSAMRecord;
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import org.broadinstitute.sting.utils.sam.ReadUtils;
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import org.broadinstitute.sting.utils.variantcontext.Allele;
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import org.broadinstitute.sting.utils.variantcontext.Genotype;
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import org.broadinstitute.sting.utils.variantcontext.GenotypeBuilder;
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@ -91,12 +92,13 @@ public class DepthPerAlleleBySample extends GenotypeAnnotation implements Standa
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alleleCounts.put(allele, 0);
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}
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for (Map.Entry<GATKSAMRecord,Map<Allele,Double>> el : perReadAlleleLikelihoodMap.getLikelihoodReadMap().entrySet()) {
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final GATKSAMRecord read = el.getKey();
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final Allele a = PerReadAlleleLikelihoodMap.getMostLikelyAllele(el.getValue());
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if (a.isNoCall())
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continue; // read is non-informative
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if (!vc.getAlleles().contains(a))
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continue; // sanity check - shouldn't be needed
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alleleCounts.put(a,alleleCounts.get(a)+1);
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alleleCounts.put(a, alleleCounts.get(a) + (read.isReducedRead() ? read.getReducedCount(ReadUtils.getReadCoordinateForReferenceCoordinate(read, vc.getStart(), ReadUtils.ClippingTail.RIGHT_TAIL)) : 1));
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}
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final int[] counts = new int[alleleCounts.size()];
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counts[0] = alleleCounts.get(vc.getReference());
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