snp_by_chr | R Documentation |
The real worker. This extracts positions for a single chromosome and puts them into a parallelizable data structure.
snp_by_chr(observations, chr_name = "01", limit = 1)
observations |
A set of observations by position to look through |
chr_name |
Chromosome name to search |
limit |
Minimum number of median hits/position to count as a snp. |
A list of variant positions where each element is one chromosome.
[Vennerable]
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