Category

Genome Variant Analysis


Usage

java -jar GenomeAnalysisTK.jar -T DepthOfCoverage -R reference.fasta -o file_name_base -I input_bams.list [-geneList refSeq.sorted.txt] [-pt readgroup] [-ct 4 -ct 6 -ct 10] [-L my_capture_genes.interval_list]


Manual

Argument name(s)Default valueSummary
Optional Outputs
--out
 -o
NoneAn output file created by the walker. Will overwrite contents if file exists
Optional Parameters
--calculateCoverageOverGenes
 -geneList
NACalculate coverage statistics over this list of genes
--countType
COUNT_READSHow should overlapping reads from the same fragment be handled?
--maxBaseQuality
127Maximum quality of bases to count towards depth
--maxMappingQuality
2147483647Maximum mapping quality of reads to count towards depth
--minBaseQuality
 -mbq
-1Minimum quality of bases to count towards depth
--minMappingQuality
 -mmq
-1Minimum mapping quality of reads to count towards depth
--outputFormat
rtableThe format of the output file
--partitionType
 -pt
[sample]Partition type for depth of coverage
Optional Flags
--omitDepthOutputAtEachBase
 -omitBaseOutput
falseDo not output depth of coverage at each base
--omitIntervalStatistics
 -omitIntervals
falseDo not calculate per-interval statistics
--omitLocusTable
falseDo not calculate per-sample per-depth counts of loci
--omitPerSampleStats
 -omitSampleSummary
falseDo not output the summary files per-sample
--printBaseCounts
 -baseCounts
falseAdd base counts to per-locus output
Advanced Parameters
--nBins
499Number of bins to use for granular binning
--start
1Starting (left endpoint) for granular binning
--stop
500Ending (right endpoint) for granular binning
--summaryCoverageThreshold
 -ct
[15]Coverage threshold (in percent) for summarizing statistics
Advanced Flags
--ignoreDeletionSites
falseIgnore sites consisting only of deletions
--includeDeletions
 -dels
falseInclude information on deletions
--includeRefNSites
falseInclude sites where the reference is N
--printBinEndpointsAndExit
falsePrint the bin values and exit immediately


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