Tools for Exploratory Analysis of Variant Calls


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Documentation for package ‘VariantTools’ version 1.48.0

Help Pages

%variant_in% Match variants by position and allele
%variant_in%-method Match variants by position and allele
annotateWithControlDepth Annotate Case with Control Depth
calculateConcordanceMatrix Variant Concordance
calculateVariantConcordance Variant Concordance
callGenotypes Call Genotypes
callGenotypes-method Call Genotypes
CallGenotypesParam Call Genotypes
callSampleSpecificVariants Call Sample-Specific Variants
callSampleSpecificVariants-method Call Sample-Specific Variants
callVariantConcordance Variant Concordance
callVariants Call Variants
callVariants-method Call Variants
callWildtype Calling Wildtype
coverage_H1993 Vignette Data
coverage_H2073 Vignette Data
DepthFETFilter Variant Filter Constructors
extractCoverageForPositions Get Coverage at Positions
genome_p53 Vignette Data
matchVariants Match variants by position and allele
MaxControlFreqFilter Variant Filter Constructors
minCallableCoverage Calling Wildtype
MinTotalDepthFilter Variant Filter Constructors
p53 Vignette Data
pileupVariants Nucleotide pileup from alignments
postFilterVariants Post-filtering of Variants
qaVariants QA Filtering of Variants
SampleSpecificVariantFilters Call Sample-Specific Variants
SetdiffVariantsFilter Variant Filter Constructors
tallies_H1993 Vignette Data
tallies_H2073 Vignette Data
tallyVariants Tally the positions in a BAM file
tallyVariants-method Tally the positions in a BAM file
TallyVariantsParam Tally the positions in a BAM file
VariantCallingFilters Call Variants
variantGR2Vcf Create a VCF for some variants
VariantPostFilters Post-filtering of Variants
VariantQAFilters QA Filtering of Variants
VariantTallyParam Tally the positions in a BAM file