Examples with Allele htsjdk.variant.variantcontext.Allele used on opensource projects

Example 31 with Allele

use of htsjdk.variant.variantcontext.Allele in project gatk by broadinstitute.

the class ReadThreadingAssembler method composeGivenHaplotypes.

/**
     * Create the list of artificial GGA-mode haplotypes by injecting each of the provided alternate alleles into the reference haplotype
     *
     * @param refHaplotype the reference haplotype
     * @param givenHaplotypes the list of alternate alleles in VariantContexts
     * @param activeRegionWindow the window containing the reference haplotype
     *
     * @return a non-null list of haplotypes
     */
private static List<Haplotype> composeGivenHaplotypes(final Haplotype refHaplotype, final List<VariantContext> givenHaplotypes, final SimpleInterval activeRegionWindow) {
    Utils.nonNull(refHaplotype, "the reference haplotype cannot be null");
    Utils.nonNull(givenHaplotypes, "given haplotypes cannot be null");
    Utils.nonNull(activeRegionWindow, "active region window cannot be null");
    Utils.validateArg(activeRegionWindow.size() == refHaplotype.length(), "inconsistent reference haplotype and active region window");
    final Set<Haplotype> returnHaplotypes = new LinkedHashSet<>();
    final int activeRegionStart = refHaplotype.getAlignmentStartHapwrtRef();
    for (final VariantContext compVC : givenHaplotypes) {
        Utils.validateArg(GATKVariantContextUtils.overlapsRegion(compVC, activeRegionWindow), " some variant provided does not overlap with active region window");
        for (final Allele compAltAllele : compVC.getAlternateAlleles()) {
            final Haplotype insertedRefHaplotype = refHaplotype.insertAllele(compVC.getReference(), compAltAllele, activeRegionStart + compVC.getStart() - activeRegionWindow.getStart(), compVC.getStart());
            if (insertedRefHaplotype != null) {
                // can be null if the requested allele can't be inserted into the haplotype
                returnHaplotypes.add(insertedRefHaplotype);
            }
        }
    }
    return new ArrayList<>(returnHaplotypes);
}

Example 32 with Allele

use of htsjdk.variant.variantcontext.Allele in project gatk by broadinstitute.

the class EvaluateCopyNumberTriStateCallsIntegrationTest method checkOutputCallsWithOverlappingTruthConcordance.

private void checkOutputCallsWithOverlappingTruthConcordance(final File truthFile, final File callsFile, final File targetsFile, final File vcfOutput, final EvaluationFiltersArgumentCollection filteringOptions) {
    final List<VariantContext> truthVariants = readVCFFile(truthFile);
    final List<VariantContext> outputVariants = readVCFFile(vcfOutput);
    final List<VariantContext> callsVariants = readVCFFile(callsFile);
    final Set<String> outputSamples = outputVariants.get(0).getSampleNames();
    final TargetCollection<Target> targets = TargetArgumentCollection.readTargetCollection(targetsFile);
    for (final VariantContext truth : truthVariants) {
        final List<Target> overlappingTargets = targets.targets(truth);
        final List<VariantContext> overlappingOutput = outputVariants.stream().filter(vc -> new SimpleInterval(vc).overlaps(truth)).collect(Collectors.toList());
        final List<VariantContext> overlappingCalls = callsVariants.stream().filter(vc -> new SimpleInterval(vc).overlaps(truth)).collect(Collectors.toList());
        if (overlappingTargets.isEmpty()) {
            Assert.assertTrue(overlappingOutput.isEmpty());
            continue;
        }
        @SuppressWarnings("all") final VariantContext matchingOutput = overlappingOutput.stream().filter(vc -> new SimpleInterval(truth).equals(new SimpleInterval(vc))).findAny().get();
        final int[] sampleCallsCount = new int[CopyNumberTriStateAllele.ALL_ALLELES.size()];
        for (final String sample : outputSamples) {
            final Genotype outputGenotype = matchingOutput.getGenotype(sample);
            final List<Pair<VariantContext, Genotype>> sampleCalls = overlappingCalls.stream().map(vc -> new ImmutablePair<>(vc, vc.getGenotype(sample))).filter(p -> XHMMSegmentGenotyper.DISCOVERY_TRUE.equals(p.getRight().getExtendedAttribute(XHMMSegmentGenotyper.DISCOVERY_KEY))).filter(p -> callPassFilters(p.getLeft(), p.getRight(), targets, filteringOptions)).collect(Collectors.toList());
            final int[] expectedCounts = new int[CopyNumberTriStateAllele.ALL_ALLELES.size()];
            sampleCalls.forEach(p -> {
                expectedCounts[CopyNumberTriStateAllele.valueOf(p.getRight().getAllele(0)).index()]++;
            });
            final int[] actualCounts = GATKProtectedVariantContextUtils.getAttributeAsIntArray(outputGenotype, VariantEvaluationContext.CALLED_ALLELE_COUNTS_KEY, () -> new int[CopyNumberTriStateAllele.ALL_ALLELES.size()], 0);
            Assert.assertEquals(actualCounts, expectedCounts, Arrays.toString(actualCounts) + " " + Arrays.toString(expectedCounts));
            final int expectedTotalCount = (int) MathUtils.sum(expectedCounts);
            final int actualTotalCount = GATKProtectedVariantContextUtils.getAttributeAsInt(outputGenotype, VariantEvaluationContext.CALLED_SEGMENTS_COUNT_KEY, -1);
            Assert.assertEquals(actualTotalCount, expectedTotalCount);
            final int expectedTargetCount = sampleCalls.stream().mapToInt(p -> targets.targetCount(p.getLeft())).sum();
            final int observedTargetCount = GATKProtectedVariantContextUtils.getAttributeAsInt(outputGenotype, VariantEvaluationContext.CALLED_TARGET_COUNT_KEY, -1);
            Assert.assertEquals(observedTargetCount, expectedTargetCount);
            final Allele truthCallAllele = outputTruthAllele(outputGenotype);
            final boolean isMixed = IntStream.of(actualCounts).filter(i -> i > 0).count() > 1;
            final String evalClass = GATKProtectedVariantContextUtils.getAttributeAsString(outputGenotype, VariantEvaluationContext.EVALUATION_CLASS_KEY, null);
            if (sampleCalls.size() > 0 && !isMixed) {
                final Pair<VariantContext, Genotype> bestCall = sampleCalls.stream().sorted((p1, p2) -> -Double.compare(callGQ(p1.getRight()), callGQ(p2.getRight()))).findFirst().get();
                final CopyNumberTriStateAllele expectedCall = CopyNumberTriStateAllele.valueOf(bestCall.getRight().getAllele(0));
                final CopyNumberTriStateAllele actualCall = CopyNumberTriStateAllele.valueOf(outputGenotype.getAllele(0));
                Assert.assertEquals(actualCall, expectedCall);
                sampleCallsCount[expectedCall.index()]++;
                if (!truthCallAllele.isReference()) {
                    if (truthCallAllele.equals(actualCall)) {
                        Assert.assertEquals(evalClass, EvaluationClass.TRUE_POSITIVE.acronym);
                    } else if (!truthCallAllele.isNoCall()) {
                        Assert.assertEquals(evalClass, EvaluationClass.DISCORDANT_POSITIVE.acronym);
                    } else {
                        Assert.assertNull(evalClass);
                    }
                } else if (truthCallAllele.isReference()) {
                    Assert.assertEquals(evalClass, EvaluationClass.FALSE_POSITIVE.acronym);
                }
            } else {
                Assert.assertEquals(Allele.NO_CALL, outputGenotype.getAllele(0));
                if (sampleCalls.isEmpty()) {
                    Assert.assertEquals(evalClass, !truthCallAllele.isReference() && truthCallAllele.isCalled() ? EvaluationClass.FALSE_NEGATIVE.acronym : null);
                    Assert.assertEquals(GATKProtectedVariantContextUtils.getAttributeAsDouble(outputGenotype, VariantEvaluationContext.CALL_QUALITY_KEY, -1), 0.0);
                } else {
                    Assert.assertEquals(evalClass, !truthCallAllele.isReference() && truthCallAllele.isCalled() ? EvaluationClass.MIXED_POSITIVE.acronym : EvaluationClass.FALSE_POSITIVE.acronym);
                    final Pair<VariantContext, Genotype> bestCall = sampleCalls.stream().sorted((p1, p2) -> -Double.compare(callGQ(p1.getRight()), callGQ(p2.getRight()))).findFirst().get();
                    Assert.assertEquals(GATKProtectedVariantContextUtils.getAttributeAsDouble(outputGenotype, VariantEvaluationContext.CALL_QUALITY_KEY, -1), callGQ(bestCall.getRight()));
                }
            }
        }
        final int expectedAN = (int) MathUtils.sum(sampleCallsCount);
        final int observedAN = matchingOutput.getAttributeAsInt(VariantEvaluationContext.CALLS_ALLELE_NUMBER_KEY, -1);
        Assert.assertEquals(observedAN, expectedAN);
        final double[] expectedAF = Arrays.copyOfRange(IntStream.of(sampleCallsCount).mapToDouble(i -> expectedAN > 0 ? i / (double) expectedAN : 0.0).toArray(), 1, sampleCallsCount.length);
        final double[] observedAF = GATKProtectedVariantContextUtils.getAttributeAsDoubleArray(matchingOutput, VariantEvaluationContext.CALLS_ALLELE_FREQUENCY_KEY, () -> new double[matchingOutput.getAlternateAlleles().size()], 0.0);
        Assert.assertNotNull(observedAF);
        assertEquals(observedAF, expectedAF, 0.01);
    }
}

Example 33 with Allele

use of htsjdk.variant.variantcontext.Allele in project gatk by broadinstitute.

the class EvaluateCopyNumberTriStateCallsIntegrationTest method checkOutputCallsWithoutOverlappingTruthConcordance.

private void checkOutputCallsWithoutOverlappingTruthConcordance(final File truthFile, final File callsFile, final File targetsFile, final File vcfOutput, final EvaluationFiltersArgumentCollection filteringOptions) {
    final List<VariantContext> truthVariants = readVCFFile(truthFile);
    final List<VariantContext> outputVariants = readVCFFile(vcfOutput);
    final List<VariantContext> callsVariants = readVCFFile(callsFile);
    final Set<String> outputSamples = outputVariants.get(0).getSampleNames();
    final TargetCollection<Target> targets = TargetArgumentCollection.readTargetCollection(targetsFile);
    for (final VariantContext call : callsVariants) {
        final List<Target> overlappingTargets = targets.targets(call);
        final List<VariantContext> overlappingOutput = outputVariants.stream().filter(vc -> new SimpleInterval(vc).overlaps(call)).collect(Collectors.toList());
        final List<VariantContext> overlappingTruth = truthVariants.stream().filter(vc -> new SimpleInterval(vc).overlaps(call)).collect(Collectors.toList());
        if (!overlappingTruth.isEmpty()) {
            continue;
        }
        @SuppressWarnings("all") final Optional<VariantContext> matchingOutputOptional = overlappingOutput.stream().filter(vc -> new SimpleInterval(call).equals(new SimpleInterval(vc))).findAny();
        final VariantContext matchingOutput = matchingOutputOptional.get();
        final int[] sampleCallsCount = new int[CopyNumberTriStateAllele.ALL_ALLELES.size()];
        for (final String sample : outputSamples) {
            final Genotype outputGenotype = matchingOutput.getGenotype(sample);
            final Genotype callGenotype = call.getGenotype(sample);
            final Allele expectedCall = callGenotype.getAllele(0).isCalled() ? CopyNumberTriStateAllele.valueOf(callGenotype.getAllele(0)) : null;
            final Allele actualCall = outputGenotype.getAllele(0).isCalled() ? CopyNumberTriStateAllele.valueOf(outputGenotype.getAllele(0)) : null;
            Assert.assertEquals(expectedCall, actualCall);
            final boolean expectedDiscovered = XHMMSegmentGenotyper.DISCOVERY_TRUE.equals(GATKProtectedVariantContextUtils.getAttributeAsString(callGenotype, XHMMSegmentGenotyper.DISCOVERY_KEY, "N"));
            final boolean actualDiscovered = XHMMSegmentGenotyper.DISCOVERY_TRUE.equals(GATKProtectedVariantContextUtils.getAttributeAsString(callGenotype, XHMMSegmentGenotyper.DISCOVERY_KEY, "N"));
            Assert.assertEquals(actualDiscovered, expectedDiscovered);
            final int[] expectedCounts = new int[CopyNumberTriStateAllele.ALL_ALLELES.size()];
            if (expectedCall.isCalled() && actualDiscovered) {
                expectedCounts[CopyNumberTriStateAllele.valueOf(expectedCall).index()]++;
            }
            if (outputGenotype.hasExtendedAttribute(VariantEvaluationContext.CALLED_ALLELE_COUNTS_KEY)) {
                Assert.assertEquals(GATKProtectedVariantContextUtils.getAttributeAsIntArray(outputGenotype, VariantEvaluationContext.CALLED_ALLELE_COUNTS_KEY, () -> new int[CopyNumberTriStateAllele.ALL_ALLELES.size()], 0), expectedCounts);
            }
            if (outputGenotype.hasExtendedAttribute(VariantEvaluationContext.CALLED_SEGMENTS_COUNT_KEY)) {
                Assert.assertEquals(GATKProtectedVariantContextUtils.getAttributeAsInt(outputGenotype, VariantEvaluationContext.CALLED_SEGMENTS_COUNT_KEY, -1), expectedCall.isCalled() && actualDiscovered ? 1 : 0);
            }
            final String evalClass = GATKProtectedVariantContextUtils.getAttributeAsString(outputGenotype, VariantEvaluationContext.EVALUATION_CLASS_KEY, null);
            Assert.assertEquals(evalClass, expectedCall.isCalled() && actualDiscovered && expectedCall.isNonReference() ? EvaluationClass.UNKNOWN_POSITIVE.acronym : null);
            if (expectedCall.isCalled()) {
                sampleCallsCount[CopyNumberTriStateAllele.valueOf(expectedCall).index()]++;
            }
            Assert.assertEquals(GATKProtectedVariantContextUtils.getAttributeAsDouble(outputGenotype, VariantEvaluationContext.CALL_QUALITY_KEY, 0.0), callGQ(callGenotype), 0.01);
        }
        final int expectedAN = (int) MathUtils.sum(sampleCallsCount);
        final int observedAN = matchingOutput.getAttributeAsInt(VariantEvaluationContext.CALLS_ALLELE_NUMBER_KEY, -1);
        Assert.assertEquals(observedAN, expectedAN);
        final double[] expectedAF = Arrays.copyOfRange(IntStream.of(sampleCallsCount).mapToDouble(i -> expectedAN > 0 ? i / (double) expectedAN : 0.0).toArray(), 1, sampleCallsCount.length);
        final double[] observedAF = GATKProtectedVariantContextUtils.getAttributeAsDoubleArray(matchingOutput, VariantEvaluationContext.CALLS_ALLELE_FREQUENCY_KEY, () -> new double[matchingOutput.getAlternateAlleles().size()], 0.0);
        Assert.assertNotNull(observedAF);
        assertEquals(observedAF, expectedAF, 0.01);
        Assert.assertEquals(matchingOutput.getAttributeAsInt(VariantEvaluationContext.TRUTH_ALLELE_NUMBER_KEY, -1), 0);
    }
}

Example 34 with Allele

use of htsjdk.variant.variantcontext.Allele in project gatk by broadinstitute.

the class CopyNumberTriStateUnitTest method testAlleleListsLogic.

@Test
public void testAlleleListsLogic() {
    Assert.assertEquals(CopyNumberTriState.ALL_ALLELES.size(), CopyNumberTriState.values().length);
    Assert.assertEquals(CopyNumberTriState.ALL_ALLELES.subList(1, CopyNumberTriState.ALL_ALLELES.size()), CopyNumberTriState.ALTERNATIVE_ALLELES);
    Assert.assertFalse(CopyNumberTriState.ALTERNATIVE_ALLELES.stream().anyMatch(Allele::isReference));
    Assert.assertTrue(CopyNumberTriState.ALL_ALLELES.get(0).isReference());
    Assert.assertEquals(CopyNumberTriState.ALL_ALLELES.get(0), CopyNumberTriState.NEUTRAL.allele);
    final List<Allele> expectedOrder = new ArrayList<>();
    for (final CopyNumberTriState state : CopyNumberTriState.values()) {
        if (state == CopyNumberTriState.NEUTRAL) {
            continue;
        }
        expectedOrder.add(state.allele);
    }
    Assert.assertEquals(CopyNumberTriState.ALTERNATIVE_ALLELES, expectedOrder);
}

Example 35 with Allele

use of htsjdk.variant.variantcontext.Allele in project gatk-protected by broadinstitute.

the class GermlineProbabilityCalculatorUnitTest method testGetGermlineAltAlleleFrequencies.

@Test
public void testGetGermlineAltAlleleFrequencies() {
    final double defaultAF = 0.001;
    final double nonDefaultAF1 = 0.1;
    final double nonDefaultAF2 = 0.01;
    final Allele Aref = Allele.create("A", true);
    final Allele C = Allele.create("C");
    final Allele G = Allele.create("G");
    final Allele T = Allele.create("T");
    final String source = "SOURCE";
    final int start = 1;
    final int stop = 1;
    //biallelic, vc has the same alt allele
    final List<Allele> altAlleles1 = Arrays.asList(C);
    final VariantContext vc1 = new VariantContextBuilder(source, "1", start, stop, Arrays.asList(Aref, C)).attribute(VCFConstants.ALLELE_FREQUENCY_KEY, new double[] { nonDefaultAF1 }).make();
    final double[] af1 = GermlineProbabilityCalculator.getGermlineAltAlleleFrequencies(altAlleles1, Optional.of(vc1), defaultAF);
    Assert.assertEquals(af1.length, altAlleles1.size());
    Assert.assertEquals(af1[0], nonDefaultAF1, 0.00001);
    //biallelic, vc has different alt allele
    final List<Allele> altAlleles2 = Arrays.asList(C);
    final VariantContext vc2 = new VariantContextBuilder(source, "1", start, stop, Arrays.asList(Aref, G)).attribute(VCFConstants.ALLELE_FREQUENCY_KEY, new double[] { nonDefaultAF1 }).make();
    final double[] af2 = GermlineProbabilityCalculator.getGermlineAltAlleleFrequencies(altAlleles2, Optional.of(vc2), defaultAF);
    Assert.assertEquals(af2.length, altAlleles2.size());
    Assert.assertEquals(af2[0], defaultAF, 0.00001);
    //triallelic, same alt alleles
    final List<Allele> altAlleles3 = Arrays.asList(C, G);
    final VariantContext vc3 = new VariantContextBuilder(source, "1", start, stop, Arrays.asList(Aref, C, G)).attribute(VCFConstants.ALLELE_FREQUENCY_KEY, new double[] { nonDefaultAF1, nonDefaultAF2 }).make();
    final double[] af3 = GermlineProbabilityCalculator.getGermlineAltAlleleFrequencies(altAlleles3, Optional.of(vc3), defaultAF);
    Assert.assertEquals(af3.length, altAlleles3.size());
    Assert.assertEquals(af3[0], nonDefaultAF1, 0.00001);
    Assert.assertEquals(af3[1], nonDefaultAF2, 0.00001);
    //triallelic, same alt alleles in different order
    final List<Allele> altAlleles4 = Arrays.asList(C, G);
    final VariantContext vc4 = new VariantContextBuilder(source, "1", start, stop, Arrays.asList(Aref, G, C)).attribute(VCFConstants.ALLELE_FREQUENCY_KEY, new double[] { nonDefaultAF1, nonDefaultAF2 }).make();
    final double[] af4 = GermlineProbabilityCalculator.getGermlineAltAlleleFrequencies(altAlleles4, Optional.of(vc4), defaultAF);
    Assert.assertEquals(af4.length, altAlleles4.size());
    Assert.assertEquals(af4[0], nonDefaultAF2, 0.00001);
    Assert.assertEquals(af4[1], nonDefaultAF1, 0.00001);
    //triallelic, only one allele in common
    final List<Allele> altAlleles5 = Arrays.asList(C, G);
    final VariantContext vc5 = new VariantContextBuilder(source, "1", start, stop, Arrays.asList(Aref, C, T)).attribute(VCFConstants.ALLELE_FREQUENCY_KEY, new double[] { nonDefaultAF1, nonDefaultAF2 }).make();
    final double[] af5 = GermlineProbabilityCalculator.getGermlineAltAlleleFrequencies(altAlleles5, Optional.of(vc5), defaultAF);
    Assert.assertEquals(af5.length, altAlleles5.size());
    Assert.assertEquals(af5[0], nonDefaultAF1, 0.00001);
    Assert.assertEquals(af5[1], defaultAF, 0.00001);
}