R/helpers.R
genmap2recombfreq.Rd
Compute the pairwise recombination frequencies between all loci from genetic map positions.
genmap2recombfreq(m, nChr)
vector of centiMorgan-scale genetic positions. names(m) correspond to a SNP_ID. Since m potentially contains all chromosomes, sets recomb. freq. b/t chrom. to 0.5
number of chromosomes
potentially really large matrix of pairwise recombination frequencies between loci
names(m) must be formatted as "chr"_"id" with "chr" being integer. For example: 2_QTL1 for a locus on chr. 2. May be worth computing in an R session using multi-threaded BLAS.
Other helper:
backsolveSNPeff()
,
centerDosage()
,
crosses2predict()
,
dose2domDevGenotypic()
,
dose2domDev()
,
effectsArray2list()
,
genoVarCovarMatFunc()
,
getAF()
,
getMAF()
,
getPropHom()
,
intensity()
,
kinship()
,
maf_filter()
,
quadform()
,
remove_invariant()