本文整理汇总了Java中htsjdk.variant.variantcontext.GenotypeBuilder类的典型用法代码示例。如果您正苦于以下问题:Java GenotypeBuilder类的具体用法?Java GenotypeBuilder怎么用?Java GenotypeBuilder使用的例子?那么恭喜您, 这里精选的类代码示例或许可以为您提供帮助。
GenotypeBuilder类属于htsjdk.variant.variantcontext包,在下文中一共展示了GenotypeBuilder类的20个代码示例,这些例子默认根据受欢迎程度排序。您可以为喜欢或者感觉有用的代码点赞,您的评价将有助于我们的系统推荐出更棒的Java代码示例。
示例1: fixAD
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
/**
* Fix the AD for the given Genotype
*
* @param genotype the original Genotype
* @param alleleIndexesToUse a bitset describing whether or not to keep a given index
* @param nAllelesToUse how many alleles we are keeping
* @return a non-null Genotype
*/
private static Genotype fixAD(final Genotype genotype, final boolean[] alleleIndexesToUse, final int nAllelesToUse) {
// if it ain't broke don't fix it
if ( !genotype.hasAD() )
return genotype;
final GenotypeBuilder builder = new GenotypeBuilder(genotype);
final int[] oldAD = genotype.getAD();
if ( oldAD.length != alleleIndexesToUse.length ) {
builder.noAD();
} else {
final int[] newAD = new int[nAllelesToUse];
int currentIndex = 0;
for ( int i = 0; i < oldAD.length; i++ ) {
if ( alleleIndexesToUse[i] )
newAD[currentIndex++] = oldAD[i];
}
builder.AD(newAD);
}
return builder.make();
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:30,代码来源:GATKVariantContextUtils.java
示例2: mergeGenotypes
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
private static void mergeGenotypes(GenotypesContext mergedGenotypes, VariantContext oneVC, AlleleMapper alleleMapping, boolean uniquifySamples) {
//TODO: should we add a check for cases when the genotypeMergeOption is REQUIRE_UNIQUE
for ( final Genotype g : oneVC.getGenotypes() ) {
final String name = mergedSampleName(oneVC.getSource(), g.getSampleName(), uniquifySamples);
if ( ! mergedGenotypes.containsSample(name) ) {
// only add if the name is new
Genotype newG = g;
if ( uniquifySamples || alleleMapping.needsRemapping() ) {
final List<Allele> alleles = alleleMapping.needsRemapping() ? alleleMapping.remap(g.getAlleles()) : g.getAlleles();
newG = new GenotypeBuilder(g).name(name).alleles(alleles).make();
}
mergedGenotypes.add(newG);
}
}
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:18,代码来源:GATKVariantContextUtils.java
示例3: pruneVariantContext
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
public static VariantContextBuilder pruneVariantContext(final VariantContextBuilder builder, Collection<String> keysToPreserve ) {
final VariantContext vc = builder.make();
if ( keysToPreserve == null ) keysToPreserve = Collections.emptyList();
// VC info
final Map<String, Object> attributes = subsetAttributes(vc.getCommonInfo(), keysToPreserve);
// Genotypes
final GenotypesContext genotypes = GenotypesContext.create(vc.getNSamples());
for ( final Genotype g : vc.getGenotypes() ) {
final GenotypeBuilder gb = new GenotypeBuilder(g);
// remove AD, DP, PL, and all extended attributes, keeping just GT and GQ
gb.noAD().noDP().noPL().noAttributes();
genotypes.add(gb.make());
}
return builder.genotypes(genotypes).attributes(attributes);
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:19,代码来源:GATKVariantContextUtils.java
示例4: purgeUnallowedGenotypeAttributes
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
public static VariantContext purgeUnallowedGenotypeAttributes(VariantContext vc, Set<String> allowedAttributes) {
if ( allowedAttributes == null )
return vc;
final GenotypesContext newGenotypes = GenotypesContext.create(vc.getNSamples());
for ( final Genotype genotype : vc.getGenotypes() ) {
final Map<String, Object> attrs = new HashMap<>();
for ( final Map.Entry<String, Object> attr : genotype.getExtendedAttributes().entrySet() ) {
if ( allowedAttributes.contains(attr.getKey()) )
attrs.put(attr.getKey(), attr.getValue());
}
newGenotypes.add(new GenotypeBuilder(genotype).attributes(attrs).make());
}
return new VariantContextBuilder(vc).genotypes(newGenotypes).make();
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:17,代码来源:GATKVariantContextUtils.java
示例5: blockToVCF
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
/**
* Convert a HomRefBlock into a VariantContext
*
* @param block the block to convert
* @return a VariantContext representing the gVCF encoding for this block.
* It will return {@code null} if input {@code block} is {@code null}, indicating that there
* is no variant-context to be output into the VCF.
*/
private VariantContext blockToVCF(final HomRefBlock block) {
if ( block == null ) return null;
final VariantContextBuilder vcb = new VariantContextBuilder(block.getStartingVC());
vcb.attributes(new HashMap<String, Object>(2)); // clear the attributes
vcb.stop(block.getStop());
vcb.attribute(VCFConstants.END_KEY, block.getStop());
// create the single Genotype with GQ and DP annotations
final GenotypeBuilder gb = new GenotypeBuilder(sampleName, GATKVariantContextUtils.homozygousAlleleList(block.getRef(),block.getPloidy()));
gb.noAD().noPL().noAttributes(); // clear all attributes
gb.GQ(block.getMedianGQ());
gb.DP(block.getMedianDP());
gb.attribute(MIN_DP_FORMAT_FIELD, block.getMinDP());
gb.PL(block.getMinPLs());
// This annotation is no longer standard
//gb.attribute(MIN_GQ_FORMAT_FIELD, block.getMinGQ());
return vcb.genotypes(gb.make()).make();
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:30,代码来源:GVCFWriter.java
示例6: assignGenotype
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
/**
* Assign genotypes (GTs) to the samples in the Variant Context greedily based on the PLs
*
* @param newLikelihoods the PL array
* @param allelesToUse the list of alleles to choose from (corresponding to the PLs)
* @param numChromosomes Number of chromosomes per pool
*/
private void assignGenotype(final GenotypeBuilder gb,
final double[] newLikelihoods,
final List<Allele> allelesToUse,
final int numChromosomes) {
final int numNewAltAlleles = allelesToUse.size() - 1;
// find the genotype with maximum likelihoods
final int PLindex = numNewAltAlleles == 0 ? 0 : MathUtils.maxElementIndex(newLikelihoods);
final GenotypeLikelihoodCalculator calculator = GenotypeLikelihoodCalculators.getInstance(numChromosomes, allelesToUse.size());
final GenotypeAlleleCounts alleleCounts = calculator.genotypeAlleleCountsAt(PLindex);
gb.alleles(alleleCounts.asAlleleList(allelesToUse));
// remove PLs if necessary
if (newLikelihoods.length > MAX_LENGTH_FOR_POOL_PL_LOGGING)
gb.noPL();
// TODO - deprecated so what is the appropriate method to call?
if (numNewAltAlleles > 0)
gb.log10PError(GenotypeLikelihoods.getGQLog10FromLikelihoods(PLindex, newLikelihoods));
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:29,代码来源:GeneralPloidyExactAFCalculator.java
示例7: annotate
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
public void annotate(final RefMetaDataTracker tracker,
final AnnotatorCompatible walker,
final ReferenceContext ref,
final AlignmentContext stratifiedContext,
final VariantContext vc,
final Genotype g,
final GenotypeBuilder gb,
final PerReadAlleleLikelihoodMap alleleLikelihoodMap) {
if ( g == null || !g.isCalled() || ( stratifiedContext == null && alleleLikelihoodMap == null) )
return;
if (alleleLikelihoodMap != null && !alleleLikelihoodMap.isEmpty())
annotateWithLikelihoods(alleleLikelihoodMap, vc, gb);
else if ( stratifiedContext != null && (vc.isSNP()))
annotateWithPileup(stratifiedContext, vc, gb);
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:17,代码来源:DepthPerAlleleBySample.java
示例8: annotateWithPileup
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
private void annotateWithPileup(final AlignmentContext stratifiedContext, final VariantContext vc, final GenotypeBuilder gb) {
final HashMap<Byte, Integer> alleleCounts = new HashMap<>();
for ( final Allele allele : vc.getAlleles() )
alleleCounts.put(allele.getBases()[0], 0);
final ReadBackedPileup pileup = stratifiedContext.getBasePileup();
for ( final PileupElement p : pileup ) {
if ( alleleCounts.containsKey(p.getBase()) )
alleleCounts.put(p.getBase(), alleleCounts.get(p.getBase())+1);
}
// we need to add counts in the correct order
final int[] counts = new int[alleleCounts.size()];
counts[0] = alleleCounts.get(vc.getReference().getBases()[0]);
for (int i = 0; i < vc.getAlternateAlleles().size(); i++)
counts[i+1] = alleleCounts.get(vc.getAlternateAllele(i).getBases()[0]);
gb.AD(counts);
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:21,代码来源:DepthPerAlleleBySample.java
示例9: annotateWithLikelihoods
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
private void annotateWithLikelihoods(final PerReadAlleleLikelihoodMap perReadAlleleLikelihoodMap, final VariantContext vc, final GenotypeBuilder gb) {
final Set<Allele> alleles = new HashSet<>(vc.getAlleles());
// make sure that there's a meaningful relationship between the alleles in the perReadAlleleLikelihoodMap and our VariantContext
if ( ! perReadAlleleLikelihoodMap.getAllelesSet().containsAll(alleles) )
throw new IllegalStateException("VC alleles " + alleles + " not a strict subset of per read allele map alleles " + perReadAlleleLikelihoodMap.getAllelesSet());
final HashMap<Allele, Integer> alleleCounts = new HashMap<>();
for ( final Allele allele : vc.getAlleles() ) { alleleCounts.put(allele, 0); }
for ( final Map.Entry<GATKSAMRecord,Map<Allele,Double>> el : perReadAlleleLikelihoodMap.getLikelihoodReadMap().entrySet()) {
final MostLikelyAllele a = PerReadAlleleLikelihoodMap.getMostLikelyAllele(el.getValue(), alleles);
if (! a.isInformative() ) continue; // read is non-informative
final GATKSAMRecord read = el.getKey();
final int prevCount = alleleCounts.get(a.getMostLikelyAllele());
alleleCounts.put(a.getMostLikelyAllele(), prevCount + 1);
}
final int[] counts = new int[alleleCounts.size()];
counts[0] = alleleCounts.get(vc.getReference());
for (int i = 0; i < vc.getAlternateAlleles().size(); i++)
counts[i+1] = alleleCounts.get( vc.getAlternateAllele(i) );
gb.AD(counts);
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:26,代码来源:DepthPerAlleleBySample.java
示例10: annotate
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
@Override
public void annotate(final RefMetaDataTracker tracker,
final AnnotatorCompatible walker,
final ReferenceContext ref,
final AlignmentContext stratifiedContext,
final VariantContext vc,
final Genotype g,
final GenotypeBuilder gb,
final PerReadAlleleLikelihoodMap alleleLikelihoodMap) {
if ( ! isAppropriateInput(alleleLikelihoodMap, g) )
return;
final int[][] table = FisherStrand.getContingencyTable(Collections.singletonMap(g.getSampleName(), alleleLikelihoodMap), vc, 0);
gb.attribute(STRAND_BIAS_BY_SAMPLE_KEY_NAME, FisherStrand.getContingencyArray(table));
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:17,代码来源:StrandBiasBySample.java
示例11: annotateGenotypes
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
private GenotypesContext annotateGenotypes(final RefMetaDataTracker tracker,
final ReferenceContext ref, final Map<String, AlignmentContext> stratifiedContexts,
final VariantContext vc,
final Map<String, PerReadAlleleLikelihoodMap> stratifiedPerReadAlleleLikelihoodMap) {
if (requestedGenotypeAnnotations.isEmpty())
return vc.getGenotypes();
final GenotypesContext genotypes = GenotypesContext.create(vc.getNSamples());
for (final Genotype genotype : vc.getGenotypes()) {
AlignmentContext context = null;
PerReadAlleleLikelihoodMap perReadAlleleLikelihoodMap = null;
if (stratifiedContexts != null)
context = stratifiedContexts.get(genotype.getSampleName());
if (stratifiedPerReadAlleleLikelihoodMap != null)
perReadAlleleLikelihoodMap = stratifiedPerReadAlleleLikelihoodMap.get(genotype.getSampleName());
final GenotypeBuilder gb = new GenotypeBuilder(genotype);
for (final GenotypeAnnotation annotation : requestedGenotypeAnnotations) {
annotation.annotate(tracker, walker, ref, context, vc, genotype, gb, perReadAlleleLikelihoodMap);
}
genotypes.add(gb.make());
}
return genotypes;
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:27,代码来源:VariantAnnotatorEngine.java
示例12: annotate
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
public void annotate(final RefMetaDataTracker tracker,
final AnnotatorCompatible walker,
final ReferenceContext ref,
final AlignmentContext stratifiedContext,
final VariantContext vc,
final Genotype g,
final GenotypeBuilder gb,
final PerReadAlleleLikelihoodMap alleleLikelihoodMap){
if ( g == null || !g.isCalled() || stratifiedContext == null )
return;
int mq0 = 0;
final ReadBackedPileup pileup = stratifiedContext.getBasePileup();
for (PileupElement p : pileup ) {
if ( p.getMappingQual() == 0 )
mq0++;
}
gb.attribute(getKeyNames().get(0), mq0);
}
开发者ID:PAA-NCIC,项目名称:SparkSeq,代码行数:21,代码来源:MappingQualityZeroBySample.java
示例13: annotateWithPileup
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
private void annotateWithPileup(final Pileup pileup, final VariantContext vc, final GenotypeBuilder gb) {
//System.out.println("annotated with pileup");
HashMap<Byte, Integer> alleleCounts = new HashMap<Byte, Integer>();
for ( Allele allele : vc.getAlleles() ) {
alleleCounts.put(allele.getBases()[0], 0);
//System.out.println("genotype allele:" + allele.getBases()[0]);
}
for ( PileupReadInfo p : pileup.getTotalPileup() ) {
if ( alleleCounts.containsKey(p.getByteBase()) ) {
//System.out.println("pileup allele:" + p.getBase());
alleleCounts.put(p.getByteBase(), alleleCounts.get(p.getByteBase())+1);
}
}
// we need to add counts in the correct order
int[] counts = new int[alleleCounts.size()];
counts[0] = alleleCounts.get(vc.getReference().getBases()[0]);
for (int i = 0; i < vc.getAlternateAlleles().size(); i++)
counts[i+1] = alleleCounts.get(vc.getAlternateAllele(i).getBases()[0]);
gb.AD(counts);
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:24,代码来源:DepthPerAlleleBySample.java
示例14: annotate
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
public void annotate(final VariantDataTracker tracker,
final ChromosomeInformationShare ref,
final Pileup pileup,
final VariantContext vc,
final Genotype g,
final GenotypeBuilder gb,
final PerReadAlleleLikelihoodMap alleleLikelihoodMap){
if ( g == null || !g.isCalled() || pileup == null )
return;
int mq0 = 0;
for (PileupReadInfo p : pileup.getTotalPileup() ) {
if ( p.getMappingQuality() == 0 )
mq0++;
}
gb.attribute(getKeyNames().get(0), mq0);
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:19,代码来源:MappingQualityZeroBySample.java
示例15: annotate
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
public void annotate(final VariantDataTracker tracker,
final ChromosomeInformationShare ref,
final Pileup pileup,
final VariantContext vc,
final Genotype g,
final GenotypeBuilder gb,
final PerReadAlleleLikelihoodMap alleleLikelihoodMap){
if ( pileup == null )
return;
Double ratio = annotateSNP(pileup, vc, g);
if (ratio == null)
return;
gb.attribute(getKeyNames().get(0), Double.valueOf(String.format("%.2f", ratio.doubleValue())));
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:17,代码来源:AlleleBalanceBySample.java
示例16: subsetGenotypeAllelesWithLikelihoods
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
/**
* From a given genotype, subset the PLs and SACs
* @param g genotype to subset
* @param allelesToUse alleles to subset
* @param vc variant context with alleles and genotypes
* @param ploidy number of chromosomes
* @param assignGenotypes true: assign hard genotypes, false: leave as no-call
* @param newLikelihoods the PL values
* @return genotype with the subsetted PLsL and SACs
*/
private Genotype subsetGenotypeAllelesWithLikelihoods(final Genotype g, final List<Allele> allelesToUse, final VariantContext vc, int ploidy,
final boolean assignGenotypes, final double[] newLikelihoods) {
final GenotypeBuilder gb = new GenotypeBuilder(g);
final String sampleName = g.getSampleName();
// add likelihoods
gb.PL(newLikelihoods);
// get and add subsetted SACs
final int[] newSACs = subsetSACAlleles(g, allelesToUse, vc);
if (newSACs != null)
gb.attribute(GaeaVCFConstants.STRAND_COUNT_BY_SAMPLE_KEY, newSACs);
if (assignGenotypes)
assignGenotype(gb, vc, sampleName, newLikelihoods, allelesToUse, ploidy);
else
gb.alleles(GaeaGvcfVariantContextUtils.noCallAlleles(ploidy));
return gb.make();
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:31,代码来源:GeneralPloidyExactAFCalculator.java
示例17: assignGenotype
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
/**
* Assign genotypes (GTs) to the samples in the VariantContext greedily based on the PLs
*
* @param gb the GenotypeBuilder to modify
* @param vc the VariantContext
* @param sampleName the sample name
* @param newLikelihoods the PL array
* @param allelesToUse the list of alleles to choose from (corresponding to the PLs)
* @param numChromosomes Number of chromosomes per pool
*/
private void assignGenotype(final GenotypeBuilder gb,
final VariantContext vc,
final String sampleName,
final double[] newLikelihoods,
final List<Allele> allelesToUse,
final int numChromosomes) {
final int numNewAltAlleles = allelesToUse.size() - 1;
// find the genotype with maximum likelihoods
final int PLindex = numNewAltAlleles == 0 ? 0 : MathUtils.maxElementIndex(newLikelihoods);
final GenotypeLikelihoodCalculator calculator = GenotypeLikelihoodCalculators.getInstance(numChromosomes,allelesToUse.size());
final GenotypeAlleleCounts alleleCounts = calculator.genotypeAlleleCountsAt(PLindex);
gb.alleles(alleleCounts.asAlleleList(allelesToUse));
removePLsIfMaxNumPLValuesExceeded(gb, vc, sampleName, newLikelihoods);
// TODO - deprecated so what is the appropriate method to call?
if ( numNewAltAlleles > 0 )
gb.log10PError(GenotypeLikelihoods.getGQLog10FromLikelihoods(PLindex, newLikelihoods));
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:32,代码来源:GeneralPloidyExactAFCalculator.java
示例18: assignGenotype
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
/**
* Assign genotypes (GTs) to the samples in the VariantContext greedily based on the PLs
*
* @param gb the GenotypeBuilder to modify
* @param vc the VariantContext
* @param sampleName the sample name
* @param newLikelihoods the PL array
* @param allelesToUse the list of alleles to choose from (corresponding to the PLs)
* @param numChromosomes Number of chromosomes per pool
*/
private void assignGenotype(final GenotypeBuilder gb,
final VariantContext vc,
final String sampleName,
final double[] newLikelihoods,
final List<Allele> allelesToUse,
final int numChromosomes) {
final int numNewAltAlleles = allelesToUse.size() - 1;
// find the genotype with maximum likelihoods
final int PLindex = numNewAltAlleles == 0 ? 0 : GvcfMathUtils.maxElementIndex(newLikelihoods);
final GenotypeLikelihoodCalculator calculator = GenotypeLikelihoodCalculators.getInstance(numChromosomes,allelesToUse.size());
final GenotypeAlleleCounts alleleCounts = calculator.genotypeAlleleCountsAt(PLindex);
gb.alleles(alleleCounts.asAlleleList(allelesToUse));
removePLsIfMaxNumPLValuesExceeded(gb, vc, sampleName, newLikelihoods);
if ( numNewAltAlleles > 0 )
gb.log10PError(GenotypeLikelihoods.getGQLog10FromLikelihoods(PLindex, newLikelihoods));
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:31,代码来源:IndependentAllelesExactAFCalculator.java
示例19: annotateGenotypes
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
private GenotypesContext annotateGenotypes(final RefMetaDataTracker tracker, final ChromosomeInformationShare ref, final VariantContext vc) {
if (requestedGenotypeAnnotations.isEmpty())
return vc.getGenotypes();
final GenotypesContext genotypes = GenotypesContext.create(vc.getNSamples());
for (final Genotype genotype : vc.getGenotypes()) {
final GenotypeBuilder gb = new GenotypeBuilder(genotype);
for (final GenotypeAnnotation annotation : requestedGenotypeAnnotations) {
annotation.annotate(tracker, ref, vc, genotype, gb);
}
genotypes.add(gb.make());
}
return genotypes;
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:17,代码来源:VariantAnnotatorEngine.java
示例20: fixAD
import htsjdk.variant.variantcontext.GenotypeBuilder; //导入依赖的package包/类
/**
* Fix the AD for the given Genotype
*
* @param genotype
* the original Genotype
* @param alleleIndexesToUse
* a bitset describing whether or not to keep a given index
* @param nAllelesToUse
* how many alleles we are keeping
* @return a non-null Genotype
*/
private static Genotype fixAD(final Genotype genotype, final BitSet alleleIndexesToUse) {
// if it ain't broke don't fix it
if (!genotype.hasAD())
return genotype;
final GenotypeBuilder builder = new GenotypeBuilder(genotype);
final int[] oldAD = genotype.getAD();
final int[] newAD = new int[alleleIndexesToUse.cardinality()];
int currentIndex = 0;
for ( int i = alleleIndexesToUse.nextSetBit(0); i >= 0; i = alleleIndexesToUse.nextSetBit(i+1) ) {
newAD[currentIndex++] = oldAD[i];
}
return builder.AD(newAD).make();
}
开发者ID:BGI-flexlab,项目名称:SOAPgaea,代码行数:29,代码来源:GaeaGvcfVariantContextUtils.java
注:本文中的htsjdk.variant.variantcontext.GenotypeBuilder类示例整理自Github/MSDocs等源码及文档管理平台,相关代码片段筛选自各路编程大神贡献的开源项目,源码版权归原作者所有,传播和使用请参考对应项目的License;未经允许,请勿转载。 |
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