Examples with VariantConsequence com.hartwig.hmftools.common.variant.VariantConsequence used on opensource projects

Example 1 with VariantConsequence

use of com.hartwig.hmftools.common.variant.VariantConsequence in project hmftools by hartwigmedical.

the class ConsequenceDeterminerTest method worksAsExpected.

@Test
public void worksAsExpected() {
    final SortedSetMultimap<String, GenomeRegion> regionMap = TreeMultimap.create();
    GenomeRegion testRegion = GenomeRegionFactory.create(CHROMOSOME, POSITION - 10, POSITION + 10);
    regionMap.put(testRegion.chromosome(), testRegion);
    final Slicer slicer = SlicerFactory.fromRegions(regionMap);
    final Map<String, HmfGenomeRegion> transcriptMap = Maps.newHashMap();
    transcriptMap.put(TRANSCRIPT, hmfRegion());
    final ConsequenceDeterminer determiner = new ConsequenceDeterminer(slicer, transcriptMap);
    final VariantConsequence rightConsequence = VariantConsequence.MISSENSE_VARIANT;
    final VariantConsequence wrongConsequence = VariantConsequence.OTHER;
    final ImmutableVariantAnnotation.Builder annotationBuilder = createVariantAnnotationBuilder().featureID(TRANSCRIPT).featureType(ConsequenceDeterminer.FEATURE_TYPE_TRANSCRIPT).gene(GENE).hgvsCoding(HGVS_CODING).hgvsProtein(HGVS_PROTEIN);
    final VariantAnnotation rightAnnotation = annotationBuilder.consequences(Lists.newArrayList(rightConsequence)).build();
    final VariantAnnotation wrongAnnotation = annotationBuilder.consequences(Lists.newArrayList(wrongConsequence)).build();
    final ImmutableSomaticVariantImpl.Builder variantBuilder = SomaticVariantTestBuilderFactory.create().chromosome(CHROMOSOME).ref(REF).alt(ALT).cosmicID(COSMIC_ID).totalReadCount(TOTAL_READ_COUNT).alleleReadCount(ALLELE_READ_COUNT);
    final SomaticVariant rightVariant = variantBuilder.position(POSITION).annotations(Lists.newArrayList(rightAnnotation)).build();
    final SomaticVariant wrongConsequenceVariant = variantBuilder.position(POSITION).annotations(Lists.newArrayList(wrongAnnotation)).build();
    final SomaticVariant wrongPositionVariant = variantBuilder.position(WRONG_POSITION).annotations(Lists.newArrayList(rightAnnotation)).build();
    final List<VariantReport> findings = determiner.run(Lists.newArrayList(rightVariant, wrongConsequenceVariant, wrongPositionVariant)).findings();
    assertEquals(1, findings.size());
    final VariantReport report = findings.get(0);
    assertEquals(GENE, report.gene());
    assertEquals(CHROMOSOME + ":" + POSITION, report.variant().chromosomePosition());
    assertEquals(REF, report.variant().ref());
    assertEquals(ALT, report.variant().alt());
    assertEquals(TRANSCRIPT + "." + TRANSCRIPT_VERSION, report.transcript());
    assertEquals(HGVS_CODING, report.hgvsCoding());
    assertEquals(HGVS_PROTEIN, report.hgvsProtein());
    assertEquals(rightConsequence.readableSequenceOntologyTerm(), report.consequence());
    assertEquals(COSMIC_ID, report.cosmicID());
    assertEquals(TOTAL_READ_COUNT, report.totalReadCount());
    assertEquals(ALLELE_READ_COUNT, report.alleleReadCount());
}

Example 2 with VariantConsequence

use of com.hartwig.hmftools.common.variant.VariantConsequence in project hmftools by hartwigmedical.

the class VariantAnnotationFactory method toConsequences.

@NotNull
private static List<VariantConsequence> toConsequences(@NotNull final List<String> effects) {
    final List<VariantConsequence> consequences = Lists.newArrayList();
    for (final String part : effects) {
        boolean found = false;
        for (final VariantConsequence consequence : VariantConsequence.values()) {
            if (consequence.isParentTypeOf(part)) {
                found = true;
                consequences.add(consequence);
            }
        }
        if (!found) {
            LOGGER.warn("Could not resolve consequence: " + part);
            consequences.add(VariantConsequence.OTHER);
        }
    }
    return consequences;
}