• 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


    CompareCallableLoci

    Compare callability statistics

    Category Diagnostics and Quality Control Tools

    Traversal LocusWalker

    PartitionBy LOCUS


    Overview

    This tool can be used to evaluate how different sequence datasets compare in terms of "callability" based on the output of the CallableLoci tool.

    Input

    Two files to compare, output by two runs of CallableLoci

    Output

    A table showing the callability status of each interval of interest in the two comparison sets and whether they match.

    Usage example

     java -jar GenomeAnalysisTK.jar \
       -R reference.fasta \
       -T CompareCallableLoci \
       -comp1 callable_loci_1.bed \
       -comp2 callable_loci_2.bed \
       [-L input.intervals \]
       -o comparison.table
     

    Additional Information

    Read filters

    These Read Filters are automatically applied to the data by the Engine before processing by CompareCallableLoci.


    Command-line Arguments

    Engine arguments

    All tools inherit arguments from the GATK Engine' "CommandLineGATK" argument collection, which can be used to modify various aspects of the tool's function. For example, the -L argument directs the GATK engine to restrict processing to specific genomic intervals; or the -rf argument allows you to apply certain read filters to exclude some of the data from the analysis.

    CompareCallableLoci specific arguments

    This table summarizes the command-line arguments that are specific to this tool. For more details on each argument, see the list further down below the table or click on an argument name to jump directly to that entry in the list.

    Argument name(s) Default value Summary
    Required Inputs
    --comp1
    NA First comparison track name
    --comp2
    NA Second comparison track name
    Optional Outputs
    --out
     -o
    stdout An output file created by the walker. Will overwrite contents if file exists
    Optional Parameters
    --printstate
     -printState
    NA If provided, prints sites satisfying this state pair

    Argument details

    Arguments in this list are specific to this tool. Keep in mind that other arguments are available that are shared with other tools (e.g. command-line GATK arguments); see Inherited arguments above.


    --comp1 / -comp1

    First comparison track name

    This argument supports reference-ordered data (ROD) files in the following formats: BED

    R RodBinding[BEDFeature]  NA


    --comp2 / -comp2

    Second comparison track name

    This argument supports reference-ordered data (ROD) files in the following formats: BED

    R RodBinding[BEDFeature]  NA


    --out / -o

    An output file created by the walker. Will overwrite contents if file exists

    PrintStream  stdout


    --printstate / -printState

    If provided, prints sites satisfying this state pair

    String  NA