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 String update1(
VariantContext vc1,
RefMetaDataTracker tracker,
ReferenceContext ref,
AlignmentContext context) {
nCalledLoci++;
// Note from Eric:
// This is really not correct. What we really want here is a polymorphic vs. monomorphic count
// (i.e. on the Genotypes).
// So in order to maintain consistency with the previous implementation (and the intention of
// the original author), I've
// added in a proxy check for monomorphic status here.
// Protect against case when vc only as no-calls too - can happen if we strafity by sample and
// sample as a single no-call.
if (vc1.isMonomorphicInSamples()) {
nRefLoci++;
} else {
switch (vc1.getType()) {
case NO_VARIATION:
// shouldn't get here
break;
case SNP:
nVariantLoci++;
nSNPs++;
if (vc1.getAttributeAsBoolean("ISSINGLETON", false)) nSingletons++;
break;
case MNP:
nVariantLoci++;
nMNPs++;
if (vc1.getAttributeAsBoolean("ISSINGLETON", false)) nSingletons++;
break;
case INDEL:
nVariantLoci++;
if (vc1.isSimpleInsertion()) nInsertions++;
else if (vc1.isSimpleDeletion()) nDeletions++;
else nComplex++;
break;
case MIXED:
nVariantLoci++;
nMixed++;
break;
case SYMBOLIC:
nSymbolic++;
break;
default:
throw new ReviewedStingException("Unexpected VariantContext type " + vc1.getType());
}
}
String refStr = vc1.getReference().getBaseString().toUpperCase();
String aaStr =
vc1.hasAttribute("ANCESTRALALLELE")
? vc1.getAttributeAsString("ANCESTRALALLELE", null).toUpperCase()
: null;
// if (aaStr.equals(".")) {
// aaStr = refStr;
// }
// ref aa alt class
// A C A der homozygote
// A C C anc homozygote
// A A A ref homozygote
// A A C
// A C A
// A C C
for (final Genotype g : vc1.getGenotypes()) {
final String altStr =
vc1.getAlternateAlleles().size() > 0
? vc1.getAlternateAllele(0).getBaseString().toUpperCase()
: null;
switch (g.getType()) {
case NO_CALL:
nNoCalls++;
break;
case HOM_REF:
nHomRef++;
if (aaStr != null && altStr != null && !refStr.equalsIgnoreCase(aaStr)) {
nHomDerived++;
}
break;
case HET:
nHets++;
break;
case HOM_VAR:
nHomVar++;
if (aaStr != null && altStr != null && !altStr.equalsIgnoreCase(aaStr)) {
nHomDerived++;
}
break;
case MIXED:
break;
default:
throw new ReviewedStingException("BUG: Unexpected genotype type: " + g);
}
}
return null; // we don't capture any interesting sites
}
