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License: BSD 3-Clause "New" or "Revised" License
Accurate matching of variant alleles using local haplotypes
License: BSD 3-Clause "New" or "Revised" License
Currently a unified database VCF is required. But for some reference panels VCFs are provided chromosome-by-chromosome. Concatenating them is an additional cost, so it'll be nice to allow multiple db VCFs (either a file containing paths, or multiple arguments, or both).
Currently only AF
is supported. It'll be nice to support other tags. Remember to check if the database VCF contains the tag when implementing.
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