Counts of genotypes: map from list of GenotypeAllele (of size ploidy) -> count
Map from ReferenceAndAlternate -> count where ReferenceAndAlternate is a single base variant.
Count of multiple nucleotide variants (e.g.: AA -> TG)
Count of insertions
Count of deletions
Sum of read depths for all genotypes with a called variant
Number of genotypes with phasing information
Count of deletions
Counts of genotypes: map from list of GenotypeAllele (of size ploidy) -> count
Count of insertions
Count of multiple nucleotide variants (e.
Count of multiple nucleotide variants (e.g.: AA -> TG)
Number of genotypes with phasing information
Sum of read depths for all genotypes with a called variant
Map from ReferenceAndAlternate -> count where ReferenceAndAlternate is a single base variant.
Simple counts of various properties across a set of genotypes.
Note: for counts of variants, both homozygous and heterozygous count as 1 (i.e. homozygous alternate is NOT counted as 2). This seems to be the most common convention.
Counts of genotypes: map from list of GenotypeAllele (of size ploidy) -> count
Map from ReferenceAndAlternate -> count where ReferenceAndAlternate is a single base variant.
Count of multiple nucleotide variants (e.g.: AA -> TG)
Count of insertions
Count of deletions
Sum of read depths for all genotypes with a called variant
Number of genotypes with phasing information