Convert genotype likelihoods to genotype probabilities
Manipulate Variant Call Format (Vcf) files.
Defunct Functions in Package 'VariantAnnotation'
Convert genotype calls from a VCF file to a SnpMatrix object
Identification of genomic variant types.
Predict amino acid coding changes for variants
Convert posterior genotype probability to a SnpMatrix object
Counts and distribution statistics for SNPs in a VCF object