sample the variant was called on
chromosome or genome contig of the variant
start position of the variant (0-based)
allele (ref + seq bases) for this variant
supporting statistics for the variant
length of the variant
allele (ref + seq bases) for this variant
allele (ref + seq bases) for this variant
Conversion to ADAMVariant
Conversion to ADAMVariant
Comparisons between ranges.
Comparisons between ranges. Order is DESCENDING (i.e. reversed) from by start.
chromosome or genome contig of the variant
chromosome or genome contig of the variant
The end position on the genome, *exclusive*.
The end position on the genome, *exclusive*. Must be non-negative.
supporting statistics for the variant
Iterate through elements in the range.
Iterate through elements in the range.
length of the variant
length of the variant
Does the region overlap another reference region
Does the region overlap another reference region
another region on the genome
True if the the regions overlap
Does the region overlap the given locus, with halfWindowSize padding?
Does the region overlap the given locus, with halfWindowSize padding?
sample the variant was called on
sample the variant was called on
start position of the variant (0-based)
start position of the variant (0-based)
A variant that exists in the sample; includes supporting read statistics
sample the variant was called on
chromosome or genome contig of the variant
start position of the variant (0-based)
allele (ref + seq bases) for this variant
supporting statistics for the variant
length of the variant