Use genetic maps available at https://github.com/joepickrell/1000-genomes-genetic-maps/ to interpolate physical positions (in bp) to genetic positions (in cM).

snp_asGeneticPos(
infos.chr,
infos.pos,
dir = tempdir(),
ncores = 1,
rsid = NULL,
type = c("OMNI", "hapmap")
)

## Arguments

infos.chr Vector of integers specifying each SNP's chromosome. Typically $map$chromosome. Vector of integers specifying the physical position on a chromosome (in base pairs) of each SNP. Typically $map$physical.pos. Directory where to download and decompress files. Default is tempdir(). Directly use uncompressed files there if already present. You can use R.utils::gunzip() to uncompress local files. Number of cores used. Default doesn't use parallelism. You may use nb_cores. If providing rsIDs, the matching is performed using those (instead of positions) and variants not matched are interpolated using spline interpolation of variants that have been matched. Whether to use the genetic maps interpolated from "OMNI" (the default), or from "hapmap".

## Value

The new vector of genetic positions.