Sample specific pileup and read statistics in support of a given variant
A variant that exists in the sample; includes supporting read statistics
A variant that exists in a tumor sample, but not in the normal sample; includes supporting read statistics from both samples
A Genotype is a map of alleles to their allele frequency
Arguments for writing output genotypes.
Caller-interface that writes computed variants to disk according to a GenotypeOutputArgs.
Base properties of a genomic change in a sequence sample from a reference genome
As a convenience to users experimenting with different callers, some variant callers include functionality to compare the called variants to a gold standard VCF after they are computed, in the same job.
Classes to represent the results of variant calling.