backsolveSNPeff: Compute ridge-regression equivalent marker effects from GBLUP...

In wolfemd/genomicMateSelectR: Genomic Mate Selection

Compute ridge-regression equivalent marker effects from GBLUP results ("Backsolve SNP effects")

Description

From the GBLUP solutions and a centered SNP matrix backsolve SNP effects

Usage

backsolveSNPeff(Z, g)

Arguments

Z	Centered marker matrix (dominance deviations must also be centered)
g	The solutions (blups, i.e. GEBVs) from the GBLUP model

Value

matrix of SNP effects matching RR-BLUP / SNP-BLUP

See Also

Other helper: centerDosage(), crosses2predict(), dose2domDevGenotypic(), dose2domDev(), effectsArray2list(), genmap2recombfreq(), genoVarCovarMatFunc(), getAF(), getMAF(), getPropHom(), intensity(), kinship(), maf_filter(), quadform(), remove_invariant()

wolfemd/genomicMateSelectR documentation built on July 1, 2022, 10:42 p.m.