コード例 #1
0
ファイル: IndelType.java プロジェクト: johandahlberg/gatk
  public Map<String, Object> annotate(
      final RefMetaDataTracker tracker,
      final AnnotatorCompatible walker,
      final ReferenceContext ref,
      final Map<String, AlignmentContext> stratifiedContexts,
      final VariantContext vc,
      final Map<String, PerReadAlleleLikelihoodMap> stratifiedPerReadAlleleLikelihoodMap) {

    int run;
    if (vc.isMixed()) {
      Map<String, Object> map = new HashMap<String, Object>();
      map.put(getKeyNames().get(0), String.format("%s", "MIXED"));
      return map;

    } else if (vc.isIndel()) {
      String type = "";
      if (!vc.isBiallelic()) type = "MULTIALLELIC_INDEL";
      else {
        if (vc.isSimpleInsertion()) type = "INS.";
        else if (vc.isSimpleDeletion()) type = "DEL.";
        else type = "OTHER.";
        ArrayList<Integer> inds = IndelUtils.findEventClassificationIndex(vc, ref);
        for (int k : inds) {
          type = type + IndelUtils.getIndelClassificationName(k) + ".";
        }
      }
      Map<String, Object> map = new HashMap<String, Object>();
      map.put(getKeyNames().get(0), String.format("%s", type));
      return map;

    } else {
      return null;
    }
  }
 public static BaseUtils.BaseSubstitutionType getSNPSubstitutionType(VariantContext context) {
   if (!context.isSNP() || !context.isBiallelic())
     throw new IllegalStateException(
         "Requested SNP substitution type for bialleic non-SNP " + context);
   return BaseUtils.SNPSubstitutionType(
       context.getReference().getBases()[0], context.getAlternateAllele(0).getBases()[0]);
 }
コード例 #3
0
ファイル: InbreedingCoeff.java プロジェクト: jwills/gatk
  private Map<String, Object> calculateIC(final VariantContext vc) {
    final GenotypesContext genotypes =
        (founderIds == null || founderIds.isEmpty())
            ? vc.getGenotypes()
            : vc.getGenotypes(founderIds);
    if (genotypes == null || genotypes.size() < MIN_SAMPLES) return null;

    int idxAA = 0, idxAB = 1, idxBB = 2;

    if (!vc.isBiallelic()) {
      // for non-bliallelic case, do test with most common alt allele.
      // Get then corresponding indeces in GL vectors to retrieve GL of AA,AB and BB.
      int[] idxVector = vc.getGLIndecesOfAlternateAllele(vc.getAltAlleleWithHighestAlleleCount());
      idxAA = idxVector[0];
      idxAB = idxVector[1];
      idxBB = idxVector[2];
    }

    double refCount = 0.0;
    double hetCount = 0.0;
    double homCount = 0.0;
    int N = 0; // number of samples that have likelihoods
    for (final Genotype g : genotypes) {
      if (g.isNoCall() || !g.hasLikelihoods()) continue;

      if (g.getPloidy() != 2) // only work for diploid samples
      continue;

      N++;
      final double[] normalizedLikelihoods =
          MathUtils.normalizeFromLog10(g.getLikelihoods().getAsVector());
      refCount += normalizedLikelihoods[idxAA];
      hetCount += normalizedLikelihoods[idxAB];
      homCount += normalizedLikelihoods[idxBB];
    }

    if (N < MIN_SAMPLES) {
      return null;
    }

    final double p =
        (2.0 * refCount + hetCount)
            / (2.0 * (refCount + hetCount + homCount)); // expected reference allele frequency
    final double q = 1.0 - p; // expected alternative allele frequency
    final double F = 1.0 - (hetCount / (2.0 * p * q * (double) N)); // inbreeding coefficient

    Map<String, Object> map = new HashMap<String, Object>();
    map.put(getKeyNames().get(0), String.format("%.4f", F));
    return map;
  }
コード例 #4
0
ファイル: VariantSummary.java プロジェクト: sbaheti/gatk
  public void update2(
      VariantContext eval,
      VariantContext comp,
      RefMetaDataTracker tracker,
      ReferenceContext ref,
      AlignmentContext context) {
    if (eval == null || (getWalker().ignoreAC0Sites() && eval.isMonomorphicInSamples())) return;

    final Type type = getType(eval);
    if (type == null) return;

    TypeSampleMap titvTable = null;

    // update DP, if possible
    if (eval.hasAttribute(VCFConstants.DEPTH_KEY)) depthPerSample.inc(type, ALL);

    // update counts
    allVariantCounts.inc(type, ALL);

    // type specific calculations
    if (type == Type.SNP && eval.isBiallelic()) {
      titvTable =
          VariantContextUtils.isTransition(eval) ? transitionsPerSample : transversionsPerSample;
      titvTable.inc(type, ALL);
    }

    // novelty calculation
    if (comp != null || (type == Type.CNV && overlapsKnownCNV(eval)))
      knownVariantCounts.inc(type, ALL);

    // per sample metrics
    for (final Genotype g : eval.getGenotypes()) {
      if (!g.isNoCall() && !g.isHomRef()) {
        countsPerSample.inc(type, g.getSampleName());

        // update transition / transversion ratio
        if (titvTable != null) titvTable.inc(type, g.getSampleName());

        if (g.hasDP()) depthPerSample.inc(type, g.getSampleName());
      }
    }
  }
コード例 #5
0
 public static boolean canBeOutputToBeagle(VariantContext v) {
   return v != null && !v.isFiltered() && v.isBiallelic() && v.hasGenotypes();
 }
コード例 #6
0
ファイル: SelectVariants.java プロジェクト: singerma/gatk
  /**
   * Subset VC record if necessary and emit the modified record (provided it satisfies criteria for
   * printing)
   *
   * @param tracker the ROD tracker
   * @param ref reference information
   * @param context alignment info
   * @return 1 if the record was printed to the output file, 0 if otherwise
   */
  @Override
  public Integer map(RefMetaDataTracker tracker, ReferenceContext ref, AlignmentContext context) {
    if (tracker == null) return 0;

    Collection<VariantContext> vcs =
        tracker.getValues(variantCollection.variants, context.getLocation());

    if (vcs == null || vcs.size() == 0) {
      return 0;
    }

    for (VariantContext vc : vcs) {
      if (MENDELIAN_VIOLATIONS) {
        boolean foundMV = false;
        for (MendelianViolation mv : mvSet) {
          if (mv.isViolation(vc)) {
            foundMV = true;
            // System.out.println(vc.toString());
            if (outMVFile != null)
              outMVFileStream.format(
                  "MV@%s:%d. REF=%s, ALT=%s, AC=%d, momID=%s, dadID=%s, childID=%s, momG=%s, momGL=%s, dadG=%s, dadGL=%s, "
                      + "childG=%s childGL=%s\n",
                  vc.getChr(),
                  vc.getStart(),
                  vc.getReference().getDisplayString(),
                  vc.getAlternateAllele(0).getDisplayString(),
                  vc.getChromosomeCount(vc.getAlternateAllele(0)),
                  mv.getSampleMom(),
                  mv.getSampleDad(),
                  mv.getSampleChild(),
                  vc.getGenotype(mv.getSampleMom()).toBriefString(),
                  vc.getGenotype(mv.getSampleMom()).getLikelihoods().getAsString(),
                  vc.getGenotype(mv.getSampleDad()).toBriefString(),
                  vc.getGenotype(mv.getSampleMom()).getLikelihoods().getAsString(),
                  vc.getGenotype(mv.getSampleChild()).toBriefString(),
                  vc.getGenotype(mv.getSampleChild()).getLikelihoods().getAsString());
          }
        }

        if (!foundMV) break;
      }
      if (DISCORDANCE_ONLY) {
        Collection<VariantContext> compVCs =
            tracker.getValues(discordanceTrack, context.getLocation());
        if (!isDiscordant(vc, compVCs)) return 0;
      }
      if (CONCORDANCE_ONLY) {
        Collection<VariantContext> compVCs =
            tracker.getValues(concordanceTrack, context.getLocation());
        if (!isConcordant(vc, compVCs)) return 0;
      }

      if (alleleRestriction.equals(NumberAlleleRestriction.BIALLELIC) && !vc.isBiallelic())
        continue;

      if (alleleRestriction.equals(NumberAlleleRestriction.MULTIALLELIC) && vc.isBiallelic())
        continue;

      if (!selectedTypes.contains(vc.getType())) continue;

      VariantContext sub = subsetRecord(vc, samples);
      if ((sub.isPolymorphic() || !EXCLUDE_NON_VARIANTS)
          && (!sub.isFiltered() || !EXCLUDE_FILTERED)) {
        for (VariantContextUtils.JexlVCMatchExp jexl : jexls) {
          if (!VariantContextUtils.match(sub, jexl)) {
            return 0;
          }
        }
        if (SELECT_RANDOM_NUMBER) {
          randomlyAddVariant(++variantNumber, sub, ref.getBase());
        } else if (!SELECT_RANDOM_FRACTION
            || (GenomeAnalysisEngine.getRandomGenerator().nextDouble() < fractionRandom)) {
          vcfWriter.add(sub);
        }
      }
    }

    return 1;
  }