| 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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