setAlleles
ADAMGenotype
setAlternateAminoAcid
VariantEffect
setAlternateReadDepth
ADAMGenotype
setAncestralAllele
ADAMDatabaseVariantAnnotation
setAttributes
ADAMRecord
setBaseQRankSum
VariantCallingAnnotations
setBasesTrimmedFromEnd
ADAMRecord
setBasesTrimmedFromStart
ADAMRecord
setCigar
ADAMRecord
setClinicalSignificance
ADAMDatabaseVariantAnnotation
setClinvarId
ADAMDatabaseVariantAnnotation
setClippingRankSum
VariantCallingAnnotations
setContig
ADAMNucleotideContigFragment ADAMPileup ADAMRecord ADAMVariant
setContigLength
ADAMContig
setContigMD5
ADAMContig
setContigName
ADAMContig
setCosmicId
ADAMDatabaseVariantAnnotation
setCountAtPosition
ADAMPileup
setCulprit
VariantCallingAnnotations
setDbSnpId
ADAMDatabaseVariantAnnotation
setDescription
ADAMNucleotideContigFragment
setDownsampled
VariantCallingAnnotations
setDuplicateRead
ADAMRecord
setExclusiveEnd
ADAMVariant
setExpectedAlleleDosage
ADAMGenotype
setFailedVendorQualityChecks
ADAMRecord
setFirstOfPair
ADAMRecord
setFisherStrandBiasPValue
VariantCallingAnnotations
setFragmentNumber
ADAMNucleotideContigFragment
setFragmentSequence
ADAMNucleotideContigFragment
setFragmentStartPosition
ADAMNucleotideContigFragment
setGeneId
VariantEffect
setGeneSymbol
ADAMDatabaseVariantAnnotation
setGenotypeLikelihoods
ADAMGenotype
setGenotypeQuality
ADAMGenotype
setGerpNr
ADAMDatabaseVariantAnnotation
setGerpRs
ADAMDatabaseVariantAnnotation
setHaplotypeScore
VariantCallingAnnotations
setHgvs
VariantEffect
setInbreedingCoefficient
VariantCallingAnnotations
setIsPhased
ADAMGenotype
setMapQuality
ADAMPileup
setMapq
ADAMRecord
setMapq0Reads
VariantCallingAnnotations
setMateAlignmentStart
ADAMRecord
setMateContig
ADAMRecord
setMateMapped
ADAMRecord
setMateNegativeStrand
ADAMRecord
setMateReference
ADAMRecord
setMinReadDepth
ADAMGenotype
setMismatchingPositions
ADAMRecord
setMqRankSum
VariantCallingAnnotations
setMutationTasterPred
ADAMDatabaseVariantAnnotation
setMutationTasterScore
ADAMDatabaseVariantAnnotation
setMutationTasterScoreConverted
ADAMDatabaseVariantAnnotation
setNonReferenceLikelihoods
ADAMGenotype
setNumReverseStrand
ADAMPileup
setNumSoftClipped
ADAMPileup
setNumberOfFragmentsInContig
ADAMNucleotideContigFragment
setOmimId
ADAMDatabaseVariantAnnotation
setOrigQual
ADAMRecord
setPhaseQuality
ADAMGenotype
setPhaseSetId
ADAMGenotype
setPhylop
ADAMDatabaseVariantAnnotation
setPileup
ADAMNestedPileup
setPosition
ADAMPileup ADAMVariant
setPrimaryAlignment
ADAMRecord
setProcessingDescription
ADAMGenotype
setProperPair
ADAMRecord
setQual
ADAMRecord
setRangeLength
ADAMPileup
setRangeOffset
ADAMPileup
setReadBase
ADAMPileup
setReadDepth
ADAMGenotype VariantCallingAnnotations
setReadEnd
ADAMPileup
setReadEvidence
ADAMNestedPileup
setReadMapped
ADAMRecord
setReadName
ADAMPileup ADAMRecord
setReadNegativeStrand
ADAMRecord
setReadPaired
ADAMRecord
setReadPositionRankSum
VariantCallingAnnotations
setReadStart
ADAMPileup
setRecordGroupDescription
ADAMPileup ADAMRecord
setRecordGroupFlowOrder
ADAMPileup ADAMRecord
setRecordGroupId
ADAMRecord
setRecordGroupKeySequence
ADAMPileup ADAMRecord
setRecordGroupLibrary
ADAMPileup ADAMRecord
setRecordGroupName
ADAMRecord
setRecordGroupPlatform
ADAMPileup ADAMRecord
setRecordGroupPlatformUnit
ADAMPileup ADAMRecord
setRecordGroupPredictedMedianInsertSize
ADAMPileup ADAMRecord
setRecordGroupRunDateEpoch
ADAMPileup ADAMRecord
setRecordGroupSample
ADAMPileup ADAMRecord
setRecordGroupSequencingCenter
ADAMPileup ADAMRecord
setReferenceAllele
ADAMVariant
setReferenceAminoAcid
VariantEffect
setReferenceBase
ADAMPileup
setReferenceReadDepth
ADAMGenotype
setReferenceURL
ADAMContig
setRmsMapQ
VariantCallingAnnotations
setSampleDescription
ADAMGenotype
setSampleId
ADAMGenotype
setSangerQuality
ADAMPileup
setSecondOfPair
ADAMRecord
setSequence
ADAMRecord
setSiftPred
ADAMDatabaseVariantAnnotation
setSiftScore
ADAMDatabaseVariantAnnotation
setSiftScoreConverted
ADAMDatabaseVariantAnnotation
setSplitFromMultiAllelic
ADAMGenotype
setStart
ADAMRecord
setStrandBiasComponents
ADAMGenotype
setThousandGenomesAlleleCount
ADAMDatabaseVariantAnnotation
setThousandGenomesAlleleFrequency
ADAMDatabaseVariantAnnotation
setTranscriptId
VariantEffect
setUsedForNegativeTrainingSet
VariantCallingAnnotations
setUsedForPositiveTrainingSet
VariantCallingAnnotations
setVariant
ADAMDatabaseVariantAnnotation ADAMGenotype
setVariantAllele
ADAMVariant
setVariantCallErrorProbability
VariantCallingAnnotations
setVariantCallingAnnotations
ADAMGenotype
setVariantFilters
VariantCallingAnnotations
setVariantIsPassing
VariantCallingAnnotations
setVariantQualityByDepth
VariantCallingAnnotations
setVqslod
VariantCallingAnnotations