Comments (1)
We do not have an equivalent annotation such as DP4 found in samtools and bcftools however if you wish to calculate strandbias from these values we do have strand bias metrics calculated from those supporting reads.
Here is the list of all annotations that HaplotypeCaller can provide
AlleleFraction
AllelePseudoDepth
AS_BaseQualityRankSumTest
AS_FisherStrand
AS_InbreedingCoeff
AS_MappingQualityRankSumTest
AS_QualByDepth
AS_ReadPosRankSumTest
AS_RMSMappingQuality
AS_StrandBiasMutectAnnotation
AS_StrandOddsRatio
AssemblyComplexity
BaseQuality
BaseQualityHistogram
BaseQualityRankSumTest
ChromosomeCounts
ClippingRankSumTest
CountNs
Coverage
CycleSkipStatus
DepthPerAlleleBySample
DepthPerSampleHC
ExcessHet
FeaturizedReadSets
FisherStrand
FragmentDepthPerAlleleBySample
FragmentLength
GcContent
GenotypeSummaries
HaplotypeFilteringAnnotation
HmerIndelLength
HmerIndelNuc
HmerMotifs
InbreedingCoeff
IndelClassify
IndelLength
LikelihoodRankSumTest
MappingQuality
MappingQualityRankSumTest
MappingQualityZero
OrientationBiasReadCounts
OriginalAlignment
PossibleDeNovo
QualByDepth
RawGtCount
ReadPosition
ReadPosRankSumTest
ReferenceBases
RMSMappingQuality
SampleList
StrandBiasBySample
StrandOddsRatio
TandemRepeat
TransmittedSingleton
UniqueAltReadCount
VariantType
You can check their descriptions from the main gatk website.
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Related Issues (20)
- MarkDuplicates results in Cannot invoke "htsjdk.samtools.SAMReadGroupRecord.getReadGroupId()" HOT 2
- What about this GATK 4 pipeline script, written by Chat-GPT HOT 1
- Follow up on CNN deprecation done in the update to python 3.10. HOT 2
- Problem with PathSeqPipelineSpark : Not generating bam
- [question] Are large files only required for tests, or also required at build and run-time ? HOT 4
- gatk Funcotator error HOT 1
- CreateSomaticPanelOfNormals: multiallelic sites wrongly added to PON despite --min-sample-count set to total input samples
- GenotypeGVCFs memory issues on GATK 4.6.0.0 HOT 12
- Tests should print per-test status, otherwise it is difficult to see what tests fail or are skipped
- GermlineCNVCaller - python exited with 2 HOT 1
- Tests fail to find libgkl libraries in /usr/local/lib
- 301 tests fail, 37 are skipped
- HaplotypeCaller is reporting DP in HOMREF region differently when ploidy is set to 1 with different Interval inputs HOT 2
- PreprocessIntervals missing results HOT 1
- SortSamSpark Required array length is too large HOT 5
- Convergence Error running GATK GermlineCNVCaller cohort mode HOT 5
- alt allels error HOT 1
- Discrepancy Between IGV and VCF File for HaplotypeCaller HOT 4
- Inconsistent Handling of Artificial Reads in Allele Depth (AD) Calculation HOT 7
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