Hi Brent,
I was trying to annotate 1KGP VCFs with genotype information of archaic hominins (e.g., Altai Neanderthal). These individuals have a lot of sites that are homozygous for the reference allele, for example:
20 60343 . G .
while this site is polymorphic in 1KGP:
20 60343 . G A
These sites match but a currently not annotated unless the --permissive-overlap flag is set, which isn't ideal. I know this is an edge case, and I can't simply merge the VCFs because the inclusion of archaic hominins would mess up downstream steps.
Would be possible to handle such cases in future?
Thanks,
Aaron