recomb_map_hg {simfam} | R Documentation |
Simplified recombination maps for human genomes
Description
Human genetic recombination maps for builds 38 (GRCh38/hg38) and 37 (GRCh37/hg19, below suffixed as hg37 for simplicity although technically incorrect).
Processed each first with recomb_map_fix_ends_chr()
to shift and extrapolate to sequence ends, then simplified with recomb_map_simplify_chr()
to remove all values that can be extrapolated with an error of up to tol = 0.1
, in order to reduce their sizes and interpolation runtime.
Defaults were used, which resulted in extrapolated recombination rates close to and centered around the average of 1e-6 cM/base).
Autosomes only.
Usage
recomb_map_hg38
recomb_map_hg37
Format
A list with 22 elements (autosomes, not named), each a tibble with two columns defining the recombination map at that chromosome:
-
pos
: position in base pairs -
posg
: position in centiMorgans (cM)
An object of class list
of length 22.
Source
Raw genetic maps downloaded from this location prior to above processing: https://bochet.gcc.biostat.washington.edu/beagle/genetic_maps/
Chromosome lengths from: https://www.ncbi.nlm.nih.gov/grc/human/data