public Map<String, Object> annotate(
RefMetaDataTracker tracker,
AnnotatorCompatible walker,
ReferenceContext ref,
Map<String, AlignmentContext> stratifiedContexts,
VariantContext vc) {
if (stratifiedContexts.size()
== 0) // size 0 means that call was made by someone else and we have no data here
return null;
if (!vc.isSNP() && !vc.isIndel() && !vc.isMixed()) return null;
final AlignmentContext context =
AlignmentContextUtils.joinContexts(stratifiedContexts.values());
final int contextWingSize = Math.min((ref.getWindow().size() - 1) / 2, MIN_CONTEXT_WING_SIZE);
final int contextSize = contextWingSize * 2 + 1;
final int locus =
ref.getLocus().getStart() + (ref.getLocus().getStop() - ref.getLocus().getStart()) / 2;
final ReadBackedPileup pileup = context.getBasePileup();
// Compute all haplotypes consistent with the current read pileup
final List<Haplotype> haplotypes = computeHaplotypes(pileup, contextSize, locus, vc);
final MathUtils.RunningAverage scoreRA = new MathUtils.RunningAverage();
if (haplotypes != null) {
for (final Genotype genotype : vc.getGenotypes()) {
final AlignmentContext thisContext = stratifiedContexts.get(genotype.getSampleName());
if (thisContext != null) {
final ReadBackedPileup thisPileup = thisContext.getBasePileup();
if (vc.isSNP())
scoreRA.add(
scoreReadsAgainstHaplotypes(
haplotypes,
thisPileup,
contextSize,
locus)); // Taking the simple average of all sample's score since the score can
// be negative and the RMS doesn't make sense
else if (vc.isIndel() || vc.isMixed()) {
Double d = scoreIndelsAgainstHaplotypes(thisPileup);
if (d == null) return null;
scoreRA.add(
d); // Taking the simple average of all sample's score since the score can be
// negative and the RMS doesn't make sense
}
}
}
}
// annotate the score in the info field
final Map<String, Object> map = new HashMap<String, Object>();
map.put(getKeyNames().get(0), String.format("%.4f", scoreRA.mean()));
return map;
}
private Map<String, AlignmentContext> getFilteredAndStratifiedContexts(
UnifiedArgumentCollection UAC,
ReferenceContext refContext,
AlignmentContext rawContext,
final GenotypeLikelihoodsCalculationModel.Model model) {
if (!BaseUtils.isRegularBase(refContext.getBase())) return null;
Map<String, AlignmentContext> stratifiedContexts = null;
if (model.name().contains("INDEL")) {
final ReadBackedPileup pileup =
rawContext.getBasePileup().getMappingFilteredPileup(UAC.MIN_BASE_QUALTY_SCORE);
// don't call when there is no coverage
if (pileup.getNumberOfElements() == 0 && UAC.OutputMode != OUTPUT_MODE.EMIT_ALL_SITES)
return null;
// stratify the AlignmentContext and cut by sample
stratifiedContexts = AlignmentContextUtils.splitContextBySampleName(pileup);
} else if (model.name().contains("SNP")) {
// stratify the AlignmentContext and cut by sample
stratifiedContexts =
AlignmentContextUtils.splitContextBySampleName(rawContext.getBasePileup());
if (!(UAC.OutputMode == OUTPUT_MODE.EMIT_ALL_SITES
&& UAC.GenotypingMode
!= GenotypeLikelihoodsCalculationModel.GENOTYPING_MODE.GENOTYPE_GIVEN_ALLELES)) {
int numDeletions = 0;
for (final PileupElement p : rawContext.getBasePileup()) {
if (p.isDeletion()) numDeletions++;
}
if (((double) numDeletions) / ((double) rawContext.getBasePileup().getNumberOfElements())
> UAC.MAX_DELETION_FRACTION) {
return null;
}
}
}
return stratifiedContexts;
}
private VariantCallContext generateEmptyContext(
RefMetaDataTracker tracker,
ReferenceContext ref,
Map<String, AlignmentContext> stratifiedContexts,
AlignmentContext rawContext) {
VariantContext vc;
if (UAC.GenotypingMode
== GenotypeLikelihoodsCalculationModel.GENOTYPING_MODE.GENOTYPE_GIVEN_ALLELES) {
VariantContext vcInput =
UnifiedGenotyperEngine.getVCFromAllelesRod(
tracker, ref, rawContext.getLocation(), false, logger, UAC.alleles);
if (vcInput == null) return null;
vc =
new VariantContextBuilder(
"UG_call",
ref.getLocus().getContig(),
vcInput.getStart(),
vcInput.getEnd(),
vcInput.getAlleles())
.make();
} else {
// deal with bad/non-standard reference bases
if (!Allele.acceptableAlleleBases(new byte[] {ref.getBase()})) return null;
Set<Allele> alleles = new HashSet<Allele>();
alleles.add(Allele.create(ref.getBase(), true));
vc =
new VariantContextBuilder(
"UG_call",
ref.getLocus().getContig(),
ref.getLocus().getStart(),
ref.getLocus().getStart(),
alleles)
.make();
}
if (annotationEngine != null) {
// Note: we want to use the *unfiltered* and *unBAQed* context for the annotations
final ReadBackedPileup pileup = rawContext.getBasePileup();
stratifiedContexts = AlignmentContextUtils.splitContextBySampleName(pileup);
vc = annotationEngine.annotateContext(tracker, ref, stratifiedContexts, vc);
}
return new VariantCallContext(vc, false);
}
private ArrayList<Allele> computeConsensusAlleles(
ReferenceContext ref,
Map<String, AlignmentContext> contexts,
AlignmentContextUtils.ReadOrientation contextType) {
Allele refAllele = null, altAllele = null;
GenomeLoc loc = ref.getLocus();
ArrayList<Allele> aList = new ArrayList<Allele>();
HashMap<String, Integer> consensusIndelStrings = new HashMap<String, Integer>();
int insCount = 0, delCount = 0;
// quick check of total number of indels in pileup
for (Map.Entry<String, AlignmentContext> sample : contexts.entrySet()) {
AlignmentContext context = AlignmentContextUtils.stratify(sample.getValue(), contextType);
final ReadBackedExtendedEventPileup indelPileup = context.getExtendedEventPileup();
insCount += indelPileup.getNumberOfInsertions();
delCount += indelPileup.getNumberOfDeletions();
}
if (insCount < minIndelCountForGenotyping && delCount < minIndelCountForGenotyping)
return aList;
for (Map.Entry<String, AlignmentContext> sample : contexts.entrySet()) {
// todo -- warning, can be duplicating expensive partition here
AlignmentContext context = AlignmentContextUtils.stratify(sample.getValue(), contextType);
final ReadBackedExtendedEventPileup indelPileup = context.getExtendedEventPileup();
for (ExtendedEventPileupElement p : indelPileup.toExtendedIterable()) {
// SAMRecord read = p.getRead();
GATKSAMRecord read = ReadUtils.hardClipAdaptorSequence(p.getRead());
if (read == null) continue;
if (ReadUtils.is454Read(read)) {
continue;
}
/* if (DEBUG && p.isIndel()) {
System.out.format("Read: %s, cigar: %s, aln start: %d, aln end: %d, p.len:%d, Type:%s, EventBases:%s\n",
read.getReadName(),read.getCigar().toString(),read.getAlignmentStart(),read.getAlignmentEnd(),
p.getEventLength(),p.getType().toString(), p.getEventBases());
}
*/
String indelString = p.getEventBases();
if (p.isInsertion()) {
boolean foundKey = false;
if (read.getAlignmentEnd() == loc.getStart()) {
// first corner condition: a read has an insertion at the end, and we're right at the
// insertion.
// In this case, the read could have any of the inserted bases and we need to build a
// consensus
for (String s : consensusIndelStrings.keySet()) {
int cnt = consensusIndelStrings.get(s);
if (s.startsWith(indelString)) {
// case 1: current insertion is prefix of indel in hash map
consensusIndelStrings.put(s, cnt + 1);
foundKey = true;
break;
} else if (indelString.startsWith(s)) {
// case 2: indel stored in hash table is prefix of current insertion
// In this case, new bases are new key.
consensusIndelStrings.remove(s);
consensusIndelStrings.put(indelString, cnt + 1);
foundKey = true;
break;
}
}
if (!foundKey)
// none of the above: event bases not supported by previous table, so add new key
consensusIndelStrings.put(indelString, 1);
} else if (read.getAlignmentStart() == loc.getStart() + 1) {
// opposite corner condition: read will start at current locus with an insertion
for (String s : consensusIndelStrings.keySet()) {
int cnt = consensusIndelStrings.get(s);
if (s.endsWith(indelString)) {
// case 1: current insertion is suffix of indel in hash map
consensusIndelStrings.put(s, cnt + 1);
foundKey = true;
break;
} else if (indelString.endsWith(s)) {
// case 2: indel stored in hash table is suffix of current insertion
// In this case, new bases are new key.
consensusIndelStrings.remove(s);
consensusIndelStrings.put(indelString, cnt + 1);
foundKey = true;
break;
}
}
if (!foundKey)
// none of the above: event bases not supported by previous table, so add new key
consensusIndelStrings.put(indelString, 1);
} else {
// normal case: insertion somewhere in the middle of a read: add count to hash map
int cnt =
consensusIndelStrings.containsKey(indelString)
? consensusIndelStrings.get(indelString)
: 0;
consensusIndelStrings.put(indelString, cnt + 1);
}
} else if (p.isDeletion()) {
indelString = String.format("D%d", p.getEventLength());
int cnt =
consensusIndelStrings.containsKey(indelString)
? consensusIndelStrings.get(indelString)
: 0;
consensusIndelStrings.put(indelString, cnt + 1);
}
}
/* if (DEBUG) {
int icount = indelPileup.getNumberOfInsertions();
int dcount = indelPileup.getNumberOfDeletions();
if (icount + dcount > 0)
{
List<Pair<String,Integer>> eventStrings = indelPileup.getEventStringsWithCounts(ref.getBases());
System.out.format("#ins: %d, #del:%d\n", insCount, delCount);
for (int i=0 ; i < eventStrings.size() ; i++ ) {
System.out.format("%s:%d,",eventStrings.get(i).first,eventStrings.get(i).second);
// int k=0;
}
System.out.println();
}
} */
}
int maxAlleleCnt = 0;
String bestAltAllele = "";
for (String s : consensusIndelStrings.keySet()) {
int curCnt = consensusIndelStrings.get(s);
if (curCnt > maxAlleleCnt) {
maxAlleleCnt = curCnt;
bestAltAllele = s;
}
// if (DEBUG)
// System.out.format("Key:%s, number: %d\n",s,consensusIndelStrings.get(s) );
} // gdebug-
if (maxAlleleCnt < minIndelCountForGenotyping) return aList;
if (bestAltAllele.startsWith("D")) {
// get deletion length
int dLen = Integer.valueOf(bestAltAllele.substring(1));
// get ref bases of accurate deletion
int startIdxInReference = (int) (1 + loc.getStart() - ref.getWindow().getStart());
// System.out.println(new String(ref.getBases()));
byte[] refBases =
Arrays.copyOfRange(ref.getBases(), startIdxInReference, startIdxInReference + dLen);
if (Allele.acceptableAlleleBases(refBases)) {
refAllele = Allele.create(refBases, true);
altAllele = Allele.create(Allele.NULL_ALLELE_STRING, false);
}
} else {
// insertion case
if (Allele.acceptableAlleleBases(bestAltAllele)) {
refAllele = Allele.create(Allele.NULL_ALLELE_STRING, true);
altAllele = Allele.create(bestAltAllele, false);
}
}
if (refAllele != null && altAllele != null) {
aList.add(0, refAllele);
aList.add(1, altAllele);
}
return aList;
}
public Allele getLikelihoods(
RefMetaDataTracker tracker,
ReferenceContext ref,
Map<String, AlignmentContext> contexts,
AlignmentContextUtils.ReadOrientation contextType,
GenotypePriors priors,
Map<String, MultiallelicGenotypeLikelihoods> GLs,
Allele alternateAlleleToUse,
boolean useBAQedPileup) {
if (tracker == null) return null;
GenomeLoc loc = ref.getLocus();
Allele refAllele, altAllele;
VariantContext vc = null;
if (!ref.getLocus().equals(lastSiteVisited)) {
// starting a new site: clear allele list
alleleList.clear();
lastSiteVisited = ref.getLocus();
indelLikelihoodMap.set(new HashMap<PileupElement, LinkedHashMap<Allele, Double>>());
haplotypeMap.clear();
if (getAlleleListFromVCF) {
for (final VariantContext vc_input : tracker.getValues(UAC.alleles, loc)) {
if (vc_input != null
&& allowableTypes.contains(vc_input.getType())
&& ref.getLocus().getStart() == vc_input.getStart()) {
vc = vc_input;
break;
}
}
// ignore places where we don't have a variant
if (vc == null) return null;
alleleList.clear();
if (ignoreSNPAllelesWhenGenotypingIndels) {
// if there's an allele that has same length as the reference (i.e. a SNP or MNP), ignore
// it and don't genotype it
for (Allele a : vc.getAlleles())
if (a.isNonReference() && a.getBases().length == vc.getReference().getBases().length)
continue;
else alleleList.add(a);
} else {
for (Allele a : vc.getAlleles()) alleleList.add(a);
}
} else {
alleleList = computeConsensusAlleles(ref, contexts, contextType);
if (alleleList.isEmpty()) return null;
}
}
// protect against having an indel too close to the edge of a contig
if (loc.getStart() <= HAPLOTYPE_SIZE) return null;
// check if there is enough reference window to create haplotypes (can be an issue at end of
// contigs)
if (ref.getWindow().getStop() < loc.getStop() + HAPLOTYPE_SIZE) return null;
if (!(priors instanceof DiploidIndelGenotypePriors))
throw new StingException(
"Only diploid-based Indel priors are supported in the DINDEL GL model");
if (alleleList.isEmpty()) return null;
refAllele = alleleList.get(0);
altAllele = alleleList.get(1);
// look for alt allele that has biggest length distance to ref allele
int maxLenDiff = 0;
for (Allele a : alleleList) {
if (a.isNonReference()) {
int lenDiff = Math.abs(a.getBaseString().length() - refAllele.getBaseString().length());
if (lenDiff > maxLenDiff) {
maxLenDiff = lenDiff;
altAllele = a;
}
}
}
final int eventLength = altAllele.getBaseString().length() - refAllele.getBaseString().length();
final int hsize = (int) ref.getWindow().size() - Math.abs(eventLength) - 1;
final int numPrefBases = ref.getLocus().getStart() - ref.getWindow().getStart() + 1;
haplotypeMap =
Haplotype.makeHaplotypeListFromAlleles(
alleleList, loc.getStart(), ref, hsize, numPrefBases);
// For each sample, get genotype likelihoods based on pileup
// compute prior likelihoods on haplotypes, and initialize haplotype likelihood matrix with
// them.
// initialize the GenotypeLikelihoods
GLs.clear();
for (Map.Entry<String, AlignmentContext> sample : contexts.entrySet()) {
AlignmentContext context = AlignmentContextUtils.stratify(sample.getValue(), contextType);
ReadBackedPileup pileup = null;
if (context.hasExtendedEventPileup()) pileup = context.getExtendedEventPileup();
else if (context.hasBasePileup()) pileup = context.getBasePileup();
if (pileup != null) {
final double[] genotypeLikelihoods =
pairModel.computeReadHaplotypeLikelihoods(
pileup, haplotypeMap, ref, eventLength, getIndelLikelihoodMap());
GLs.put(
sample.getKey(),
new MultiallelicGenotypeLikelihoods(
sample.getKey(), alleleList, genotypeLikelihoods, getFilteredDepth(pileup)));
if (DEBUG) {
System.out.format("Sample:%s Alleles:%s GL:", sample.getKey(), alleleList.toString());
for (int k = 0; k < genotypeLikelihoods.length; k++)
System.out.format("%1.4f ", genotypeLikelihoods[k]);
System.out.println();
}
}
}
return refAllele;
}
/**
* Main entry function to calculate genotypes of a given VC with corresponding GL's
*
* @param tracker Tracker
* @param refContext Reference context
* @param rawContext Raw context
* @param stratifiedContexts Stratified alignment contexts
* @param vc Input VC
* @param model GL calculation model
* @param inheritAttributesFromInputVC Output VC will contain attributes inherited from input vc
* @return VC with assigned genotypes
*/
public VariantCallContext calculateGenotypes(
final RefMetaDataTracker tracker,
final ReferenceContext refContext,
final AlignmentContext rawContext,
Map<String, AlignmentContext> stratifiedContexts,
final VariantContext vc,
final GenotypeLikelihoodsCalculationModel.Model model,
final boolean inheritAttributesFromInputVC,
final Map<String, org.broadinstitute.sting.utils.genotyper.PerReadAlleleLikelihoodMap>
perReadAlleleLikelihoodMap) {
boolean limitedContext =
tracker == null || refContext == null || rawContext == null || stratifiedContexts == null;
// initialize the data for this thread if that hasn't been done yet
if (afcm.get() == null) {
afcm.set(AFCalcFactory.createAFCalc(UAC, N, logger));
}
// estimate our confidence in a reference call and return
if (vc.getNSamples() == 0) {
if (limitedContext) return null;
return (UAC.OutputMode != OUTPUT_MODE.EMIT_ALL_SITES
? estimateReferenceConfidence(vc, stratifiedContexts, getTheta(model), false, 1.0)
: generateEmptyContext(tracker, refContext, stratifiedContexts, rawContext));
}
AFCalcResult AFresult = afcm.get().getLog10PNonRef(vc, getAlleleFrequencyPriors(model));
// is the most likely frequency conformation AC=0 for all alternate alleles?
boolean bestGuessIsRef = true;
// determine which alternate alleles have AF>0
final List<Allele> myAlleles = new ArrayList<Allele>(vc.getAlleles().size());
final List<Integer> alleleCountsofMLE = new ArrayList<Integer>(vc.getAlleles().size());
myAlleles.add(vc.getReference());
for (int i = 0; i < AFresult.getAllelesUsedInGenotyping().size(); i++) {
final Allele alternateAllele = AFresult.getAllelesUsedInGenotyping().get(i);
if (alternateAllele.isReference()) continue;
// we are non-ref if the probability of being non-ref > the emit confidence.
// the emit confidence is phred-scaled, say 30 => 10^-3.
// the posterior AF > 0 is log10: -5 => 10^-5
// we are non-ref if 10^-5 < 10^-3 => -5 < -3
final boolean isNonRef =
AFresult.isPolymorphic(alternateAllele, UAC.STANDARD_CONFIDENCE_FOR_EMITTING / -10.0);
// if the most likely AC is not 0, then this is a good alternate allele to use
if (isNonRef) {
myAlleles.add(alternateAllele);
alleleCountsofMLE.add(AFresult.getAlleleCountAtMLE(alternateAllele));
bestGuessIsRef = false;
}
// if in GENOTYPE_GIVEN_ALLELES mode, we still want to allow the use of a poor allele
else if (UAC.GenotypingMode
== GenotypeLikelihoodsCalculationModel.GENOTYPING_MODE.GENOTYPE_GIVEN_ALLELES) {
myAlleles.add(alternateAllele);
alleleCountsofMLE.add(AFresult.getAlleleCountAtMLE(alternateAllele));
}
}
final double PoFGT0 = Math.pow(10, AFresult.getLog10PosteriorOfAFGT0());
// note the math.abs is necessary because -10 * 0.0 => -0.0 which isn't nice
final double phredScaledConfidence =
Math.abs(
!bestGuessIsRef
|| UAC.GenotypingMode
== GenotypeLikelihoodsCalculationModel.GENOTYPING_MODE
.GENOTYPE_GIVEN_ALLELES
? -10 * AFresult.getLog10PosteriorOfAFEq0()
: -10 * AFresult.getLog10PosteriorOfAFGT0());
// return a null call if we don't pass the confidence cutoff or the most likely allele frequency
// is zero
if (UAC.OutputMode != OUTPUT_MODE.EMIT_ALL_SITES
&& !passesEmitThreshold(phredScaledConfidence, bestGuessIsRef)) {
// technically, at this point our confidence in a reference call isn't accurately estimated
// because it didn't take into account samples with no data, so let's get a better estimate
return limitedContext
? null
: estimateReferenceConfidence(vc, stratifiedContexts, getTheta(model), true, PoFGT0);
}
// start constructing the resulting VC
final GenomeLoc loc = genomeLocParser.createGenomeLoc(vc);
final VariantContextBuilder builder =
new VariantContextBuilder(
"UG_call", loc.getContig(), loc.getStart(), loc.getStop(), myAlleles);
builder.log10PError(phredScaledConfidence / -10.0);
if (!passesCallThreshold(phredScaledConfidence)) builder.filters(filter);
// create the genotypes
final GenotypesContext genotypes = afcm.get().subsetAlleles(vc, myAlleles, true, ploidy);
builder.genotypes(genotypes);
// print out stats if we have a writer
if (verboseWriter != null && !limitedContext)
printVerboseData(refContext.getLocus().toString(), vc, PoFGT0, phredScaledConfidence, model);
// *** note that calculating strand bias involves overwriting data structures, so we do that
// last
final HashMap<String, Object> attributes = new HashMap<String, Object>();
// inherit attributed from input vc if requested
if (inheritAttributesFromInputVC) attributes.putAll(vc.getAttributes());
// if the site was downsampled, record that fact
if (!limitedContext && rawContext.hasPileupBeenDownsampled())
attributes.put(VCFConstants.DOWNSAMPLED_KEY, true);
if (UAC.ANNOTATE_NUMBER_OF_ALLELES_DISCOVERED)
attributes.put(NUMBER_OF_DISCOVERED_ALLELES_KEY, vc.getAlternateAlleles().size());
// add the MLE AC and AF annotations
if (alleleCountsofMLE.size() > 0) {
attributes.put(VCFConstants.MLE_ALLELE_COUNT_KEY, alleleCountsofMLE);
final int AN = builder.make().getCalledChrCount();
final ArrayList<Double> MLEfrequencies = new ArrayList<Double>(alleleCountsofMLE.size());
// the MLEAC is allowed to be larger than the AN (e.g. in the case of all PLs being 0, the GT
// is ./. but the exact model may arbitrarily choose an AC>1)
for (int AC : alleleCountsofMLE) MLEfrequencies.add(Math.min(1.0, (double) AC / (double) AN));
attributes.put(VCFConstants.MLE_ALLELE_FREQUENCY_KEY, MLEfrequencies);
}
if (UAC.COMPUTE_SLOD && !limitedContext && !bestGuessIsRef) {
// final boolean DEBUG_SLOD = false;
// the overall lod
// double overallLog10PofNull = AFresult.log10AlleleFrequencyPosteriors[0];
double overallLog10PofF = AFresult.getLog10LikelihoodOfAFGT0();
// if ( DEBUG_SLOD ) System.out.println("overallLog10PofF=" + overallLog10PofF);
List<Allele> allAllelesToUse = builder.make().getAlleles();
// the forward lod
VariantContext vcForward =
calculateLikelihoods(
tracker,
refContext,
stratifiedContexts,
AlignmentContextUtils.ReadOrientation.FORWARD,
allAllelesToUse,
false,
model,
perReadAlleleLikelihoodMap);
AFresult = afcm.get().getLog10PNonRef(vcForward, getAlleleFrequencyPriors(model));
// double[] normalizedLog10Posteriors =
// MathUtils.normalizeFromLog10(AFresult.log10AlleleFrequencyPosteriors, true);
double forwardLog10PofNull = AFresult.getLog10LikelihoodOfAFEq0();
double forwardLog10PofF = AFresult.getLog10LikelihoodOfAFGT0();
// if ( DEBUG_SLOD ) System.out.println("forwardLog10PofNull=" + forwardLog10PofNull + ",
// forwardLog10PofF=" + forwardLog10PofF);
// the reverse lod
VariantContext vcReverse =
calculateLikelihoods(
tracker,
refContext,
stratifiedContexts,
AlignmentContextUtils.ReadOrientation.REVERSE,
allAllelesToUse,
false,
model,
perReadAlleleLikelihoodMap);
AFresult = afcm.get().getLog10PNonRef(vcReverse, getAlleleFrequencyPriors(model));
// normalizedLog10Posteriors =
// MathUtils.normalizeFromLog10(AFresult.log10AlleleFrequencyPosteriors, true);
double reverseLog10PofNull = AFresult.getLog10LikelihoodOfAFEq0();
double reverseLog10PofF = AFresult.getLog10LikelihoodOfAFGT0();
// if ( DEBUG_SLOD ) System.out.println("reverseLog10PofNull=" + reverseLog10PofNull + ",
// reverseLog10PofF=" + reverseLog10PofF);
double forwardLod = forwardLog10PofF + reverseLog10PofNull - overallLog10PofF;
double reverseLod = reverseLog10PofF + forwardLog10PofNull - overallLog10PofF;
// if ( DEBUG_SLOD ) System.out.println("forward lod=" + forwardLod + ", reverse lod=" +
// reverseLod);
// strand score is max bias between forward and reverse strands
double strandScore = Math.max(forwardLod, reverseLod);
// rescale by a factor of 10
strandScore *= 10.0;
// logger.debug(String.format("SLOD=%f", strandScore));
if (!Double.isNaN(strandScore)) attributes.put("SB", strandScore);
}
// finish constructing the resulting VC
builder.attributes(attributes);
VariantContext vcCall = builder.make();
// if we are subsetting alleles (either because there were too many or because some were not
// polymorphic)
// then we may need to trim the alleles (because the original VariantContext may have had to pad
// at the end).
if (myAlleles.size() != vc.getAlleles().size()
&& !limitedContext) // limitedContext callers need to handle allele trimming on their own to
// keep their perReadAlleleLikelihoodMap alleles in sync
vcCall = VariantContextUtils.reverseTrimAlleles(vcCall);
if (annotationEngine != null
&& !limitedContext) { // limitedContext callers need to handle annotations on their own by
// calling their own annotationEngine
// Note: we want to use the *unfiltered* and *unBAQed* context for the annotations
final ReadBackedPileup pileup = rawContext.getBasePileup();
stratifiedContexts = AlignmentContextUtils.splitContextBySampleName(pileup);
vcCall =
annotationEngine.annotateContext(
tracker, refContext, stratifiedContexts, vcCall, perReadAlleleLikelihoodMap);
}
return new VariantCallContext(vcCall, confidentlyCalled(phredScaledConfidence, PoFGT0));
}