• Diagnostics and Quality Control Tools
  • ASEReadCounter
  • AnalyzeCovariates
  • CallableLoci
  • CheckPileup
  • CompareCallableLoci
  • ContEst
  • CountBases
  • CountIntervals
  • CountLoci
  • CountMales
  • CountRODs
  • CountRODsByRef
  • CountReadEvents
  • CountReads
  • CountTerminusEvent
  • DepthOfCoverage
  • DiagnoseTargets
  • DiffObjects
  • ErrorRatePerCycle
  • FastaStats
  • FindCoveredIntervals
  • FlagStat
  • GCContentByInterval
  • GatherBqsrReports
  • Pileup
  • PrintRODs
  • QualifyMissingIntervals
  • ReadClippingStats
  • ReadGroupProperties
  • ReadLengthDistribution
  • SimulateReadsForVariants
  • Sequence Data Processing Tools
  • BaseRecalibrator
  • ClipReads
  • IndelRealigner
  • LeftAlignIndels
  • PrintReads
  • RealignerTargetCreator
  • SplitNCigarReads
  • SplitSamFile
  • Variant Discovery Tools
  • ApplyRecalibration
  • CalculateGenotypePosteriors
  • GATKPaperGenotyper
  • GenotypeGVCFs
  • HaplotypeCaller
  • MuTect2
  • RegenotypeVariants
  • UnifiedGenotyper
  • VariantRecalibrator
  • Variant Evaluation Tools
  • GenotypeConcordance
  • ValidateVariants
  • VariantEval
  • VariantFiltration
  • Variant Manipulation Tools
  • CatVariants
  • CombineGVCFs
  • CombineVariants
  • HaplotypeResolver
  • LeftAlignAndTrimVariants
  • PhaseByTransmission
  • RandomlySplitVariants
  • ReadBackedPhasing
  • SelectHeaders
  • SelectVariants
  • ValidationSiteSelector
  • VariantAnnotator
  • VariantsToAllelicPrimitives
  • VariantsToBinaryPed
  • VariantsToTable
  • VariantsToVCF

  • Annotation Modules
  • AS_BaseQualityRankSumTest
  • AS_FisherStrand
  • AS_InbreedingCoeff
  • AS_InsertSizeRankSum
  • AS_MQMateRankSumTest
  • AS_MappingQualityRankSumTest
  • AS_QualByDepth
  • AS_RMSMappingQuality
  • AS_ReadPosRankSumTest
  • AS_StrandOddsRatio
  • AlleleBalance
  • AlleleBalanceBySample
  • AlleleCountBySample
  • BaseCounts
  • BaseCountsBySample
  • BaseQualityRankSumTest
  • BaseQualitySumPerAlleleBySample
  • ChromosomeCounts
  • ClippingRankSumTest
  • ClusteredReadPosition
  • Coverage
  • DepthPerAlleleBySample
  • DepthPerSampleHC
  • ExcessHet
  • FisherStrand
  • FractionInformativeReads
  • GCContent
  • GenotypeSummaries
  • HaplotypeScore
  • HardyWeinberg
  • HomopolymerRun
  • InbreedingCoeff
  • LikelihoodRankSumTest
  • LowMQ
  • MVLikelihoodRatio
  • MappingQualityRankSumTest
  • MappingQualityZero
  • MappingQualityZeroBySample
  • NBaseCount
  • OxoGReadCounts
  • PossibleDeNovo
  • QualByDepth
  • RMSMappingQuality
  • ReadPosRankSumTest
  • SampleList
  • SnpEff
  • SpanningDeletions
  • StrandAlleleCountsBySample
  • StrandBiasBySample
  • StrandOddsRatio
  • TandemRepeatAnnotator
  • TransmissionDisequilibriumTest
  • VariantType
  • Read Filters
  • BadCigarFilter
  • BadMateFilter
  • CountingFilteringIterator.CountingReadFilter
  • DuplicateReadFilter
  • FailsVendorQualityCheckFilter
  • HCMappingQualityFilter
  • LibraryReadFilter
  • MalformedReadFilter
  • MappingQualityFilter
  • MappingQualityUnavailableFilter
  • MappingQualityZeroFilter
  • MateSameStrandFilter
  • MaxInsertSizeFilter
  • MissingReadGroupFilter
  • NoOriginalQualityScoresFilter
  • NotPrimaryAlignmentFilter
  • OverclippedReadFilter
  • Platform454Filter
  • PlatformFilter
  • PlatformUnitFilter
  • ReadGroupBlackListFilter
  • ReadLengthFilter
  • ReadNameFilter
  • ReadStrandFilter
  • ReassignMappingQualityFilter
  • ReassignOneMappingQualityFilter
  • ReassignOriginalMQAfterIndelRealignmentFilter
  • SampleFilter
  • SingleReadGroupFilter
  • UnmappedReadFilter
  • Resource File Codecs
  • BeagleCodec
  • BedTableCodec
  • RawHapMapCodec
  • RefSeqCodec
  • SAMPileupCodec
  • SAMReadCodec
  • TableCodec

  • Reference Utilities
  • FastaAlternateReferenceMaker
  • FastaReferenceMaker
  • QCRef
  • Showing docs for version 3.7-0


    MappingQualityRankSumTest

    Rank Sum Test for mapping qualities of REF versus ALT reads

    Category Annotation Modules

    VCF Field INFO (variant-level)

    Type StandardAnnotation, ActiveRegionBasedAnnotation

    Header definition line
  • INFO=<ID=MQRankSum,Number=1,Type=Float,Description="Z-score From Wilcoxon rank sum test of Alt vs. Ref read mapping qualities">

  • Overview

    This variant-level annotation compares the mapping qualities of the reads supporting the reference allele with those supporting the alternate allele. The ideal result is a value close to zero, which indicates there is little to no difference. A negative value indicates that the reads supporting the alternate allele have lower mapping quality scores than those supporting the reference allele. Conversely, a positive value indicates that the reads supporting the alternate allele have higher mapping quality scores than those supporting the reference allele.

    This annotation can be used to evaluate confidence in a variant call and is a recommended covariate for variant recalibration (VQSR). Finding a statistically significant difference in quality either way suggests that the sequencing and/or mapping process may have been biased or affected by an artifact. In practice, we only filter out low negative values when evaluating variant quality because the idea is to filter out variants for which the quality of the data supporting the alternate allele is comparatively low. The reverse case, where it is the quality of data supporting the reference allele that is lower (resulting in positive ranksum scores), is not really informative for filtering variants.

    Statistical notes

    The value output for this annotation is the u-based z-approximation from the Mann-Whitney-Wilcoxon Rank Sum Test for mapping qualities (MAPQ of reads supporting REF vs. MAPQ of reads supporting ALT). See the method document on statistical tests for a more detailed explanation of the ranksum test.

    Caveats

    Related annotations