Examples with ReadLikelihoods org.broadinstitute.hellbender.utils.genotyper.ReadLikelihoods used on opensource projects

Example 21 with ReadLikelihoods

use of org.broadinstitute.hellbender.utils.genotyper.ReadLikelihoods in project gatk by broadinstitute.

the class RankSumTest method annotate.

@Override
public Map<String, Object> annotate(final ReferenceContext ref, final VariantContext vc, final ReadLikelihoods<Allele> likelihoods) {
    Utils.nonNull(vc, "vc is null");
    final GenotypesContext genotypes = vc.getGenotypes();
    if (genotypes == null || genotypes.isEmpty()) {
        return Collections.emptyMap();
    }
    final List<Double> refQuals = new ArrayList<>();
    final List<Double> altQuals = new ArrayList<>();
    final int refLoc = vc.getStart();
    if (likelihoods != null) {
        for (final ReadLikelihoods<Allele>.BestAllele<Allele> bestAllele : likelihoods.bestAlleles()) {
            final GATKRead read = bestAllele.read;
            final Allele allele = bestAllele.allele;
            if (bestAllele.isInformative() && isUsableRead(read, refLoc)) {
                final OptionalDouble value = getElementForRead(read, refLoc, bestAllele);
                // Bypass read if the clipping goal is not reached or the refloc is inside a spanning deletion
                if (value.isPresent() && value.getAsDouble() != INVALID_ELEMENT_FROM_READ) {
                    if (allele.isReference()) {
                        refQuals.add(value.getAsDouble());
                    } else if (vc.hasAllele(allele)) {
                        altQuals.add(value.getAsDouble());
                    }
                }
            }
        }
    }
    if (refQuals.isEmpty() && altQuals.isEmpty()) {
        return Collections.emptyMap();
    }
    final MannWhitneyU mannWhitneyU = new MannWhitneyU();
    // we are testing that set1 (the alt bases) have lower quality scores than set2 (the ref bases)
    final MannWhitneyU.Result result = mannWhitneyU.test(Doubles.toArray(altQuals), Doubles.toArray(refQuals), MannWhitneyU.TestType.FIRST_DOMINATES);
    final double zScore = result.getZ();
    if (Double.isNaN(zScore)) {
        return Collections.emptyMap();
    } else {
        return Collections.singletonMap(getKeyNames().get(0), String.format("%.3f", zScore));
    }
}

Example 22 with ReadLikelihoods

use of org.broadinstitute.hellbender.utils.genotyper.ReadLikelihoods in project gatk-protected by broadinstitute.

the class StrandArtifact method annotate.

@Override
public void annotate(final ReferenceContext ref, final VariantContext vc, final Genotype g, final GenotypeBuilder gb, final ReadLikelihoods<Allele> likelihoods) {
    Utils.nonNull(gb);
    Utils.nonNull(vc);
    Utils.nonNull(likelihoods);
    // do not annotate the genotype fields for normal
    if (g.isHomRef()) {
        return;
    }
    pi.put(NO_ARTIFACT, 0.95);
    pi.put(ART_FWD, 0.025);
    pi.put(ART_REV, 0.025);
    // We use the allele with highest LOD score
    final double[] tumorLods = GATKProtectedVariantContextUtils.getAttributeAsDoubleArray(vc, GATKVCFConstants.TUMOR_LOD_KEY, () -> null, -1);
    final int indexOfMaxTumorLod = MathUtils.maxElementIndex(tumorLods);
    final Allele altAlelle = vc.getAlternateAllele(indexOfMaxTumorLod);
    final Collection<ReadLikelihoods<Allele>.BestAllele<Allele>> bestAlleles = likelihoods.bestAlleles(g.getSampleName());
    final int numFwdAltReads = (int) bestAlleles.stream().filter(ba -> !ba.read.isReverseStrand() && ba.isInformative() && ba.allele.equals(altAlelle)).count();
    final int numRevAltReads = (int) bestAlleles.stream().filter(ba -> ba.read.isReverseStrand() && ba.isInformative() && ba.allele.equals(altAlelle)).count();
    final int numFwdReads = (int) bestAlleles.stream().filter(ba -> !ba.read.isReverseStrand() && ba.isInformative()).count();
    final int numRevReads = (int) bestAlleles.stream().filter(ba -> ba.read.isReverseStrand() && ba.isInformative()).count();
    final int numAltReads = numFwdAltReads + numRevAltReads;
    final int numReads = numFwdReads + numRevReads;
    final EnumMap<StrandArtifactZ, Double> unnormalized_posterior_probabilities = new EnumMap<>(StrandArtifactZ.class);
    final EnumMap<StrandArtifactZ, Double> maximum_a_posteriori_allele_fraction_estimates = new EnumMap<>(StrandArtifactZ.class);
    /*** Compute the posterior probability of ARTIFACT_FWD and ARTIFACT_REV; it's a double integral over f and epsilon ***/
    // the integrand is a polynomial of degree n, where n is the number of reads at the locus
    // thus to integrate exactly with Gauss-Legendre we need (n/2)+1 points
    final int numIntegPointsForAlleleFraction = numReads / 2 + 1;
    final int numIntegPointsForEpsilon = (numReads + ALPHA + BETA - 2) / 2 + 1;
    final double likelihoodForArtifactFwd = IntegrationUtils.integrate2d((f, epsilon) -> getIntegrandGivenArtifact(f, epsilon, numFwdReads, numRevReads, numFwdAltReads, numRevAltReads), 0.0, 1.0, numIntegPointsForAlleleFraction, 0.0, 1.0, numIntegPointsForEpsilon);
    final double likelihoodForArtifactRev = IntegrationUtils.integrate2d((f, epsilon) -> getIntegrandGivenArtifact(f, epsilon, numRevReads, numFwdReads, numRevAltReads, numFwdAltReads), 0.0, 1.0, numIntegPointsForAlleleFraction, 0.0, 1.0, numIntegPointsForEpsilon);
    unnormalized_posterior_probabilities.put(ART_FWD, pi.get(ART_FWD) * likelihoodForArtifactFwd);
    unnormalized_posterior_probabilities.put(ART_REV, pi.get(ART_REV) * likelihoodForArtifactRev);
    /*** Compute the posterior probability of NO_ARTIFACT; evaluate a single integral over the allele fraction ***/
    final double likelihoodForNoArtifact = IntegrationUtils.integrate(f -> getIntegrandGivenNoArtifact(f, numFwdReads, numRevReads, numFwdAltReads, numRevAltReads), 0.0, 1.0, numIntegPointsForAlleleFraction);
    unnormalized_posterior_probabilities.put(NO_ARTIFACT, pi.get(NO_ARTIFACT) * likelihoodForNoArtifact);
    final double[] posterior_probabilities = MathUtils.normalizeFromRealSpace(unnormalized_posterior_probabilities.values().stream().mapToDouble(Double::doubleValue).toArray());
    /*** Compute the maximum a posteriori estimate for allele fraction given strand artifact ***/
    // For a fixed f, integrate the double integral over epsilons. This gives us the likelihood p(x^+, x^- | f, z) for a fixed f, which is proportional to
    // the posterior probability of p(f | x^+, x^-, z)
    final int numSamplePoints = 100;
    final double[] samplePoints = GATKProtectedMathUtils.createEvenlySpacedPoints(0.0, 1.0, numSamplePoints);
    double[] likelihoodsGivenForwardArtifact = new double[numSamplePoints];
    double[] likelihoodsGivenReverseArtifact = new double[numSamplePoints];
    for (int i = 0; i < samplePoints.length; i++) {
        final double f = samplePoints[i];
        likelihoodsGivenForwardArtifact[i] = IntegrationUtils.integrate(epsilon -> getIntegrandGivenArtifact(f, epsilon, numFwdReads, numRevReads, numFwdAltReads, numRevAltReads), 0.0, 1.0, numIntegPointsForEpsilon);
        likelihoodsGivenReverseArtifact[i] = IntegrationUtils.integrate(epsilon -> getIntegrandGivenArtifact(f, epsilon, numRevReads, numFwdReads, numRevAltReads, numFwdAltReads), 0.0, 1.0, numIntegPointsForEpsilon);
    }
    final int maxAlleleFractionIndexFwd = MathUtils.maxElementIndex(likelihoodsGivenForwardArtifact);
    final int maxAlleleFractionIndexRev = MathUtils.maxElementIndex(likelihoodsGivenReverseArtifact);
    maximum_a_posteriori_allele_fraction_estimates.put(ART_FWD, samplePoints[maxAlleleFractionIndexFwd]);
    maximum_a_posteriori_allele_fraction_estimates.put(ART_REV, samplePoints[maxAlleleFractionIndexRev]);
    // In the absence of strand artifact, MAP estimate for f reduces to the sample alt allele fraction
    maximum_a_posteriori_allele_fraction_estimates.put(NO_ARTIFACT, (double) numAltReads / numReads);
    gb.attribute(POSTERIOR_PROBABILITIES_KEY, posterior_probabilities);
    gb.attribute(MAP_ALLELE_FRACTIONS_KEY, maximum_a_posteriori_allele_fraction_estimates.values().stream().mapToDouble(Double::doubleValue).toArray());
}