Publication | Closed Access
Using the genomic relationship matrix to predict the accuracy of genomic selection
352
Citations
25
References
2011
Year
GeneticsGenomic SelectionGenomicsGene RecognitionAnimal GeneticsGenomic PredictionGenome-wide Association StudyGenetic AnalysisGenomic Relationship MatrixGenotype-phenotype AssociationMolecular EcologyComputational GenomicsBreedingBiostatisticsRelationship MatrixPublic HealthPersonal GenomicsBreeding ValuesRegression CoefficientPrecision BreedingStatistical GeneticsMolecular BreedingGenetic VariationPopulation GeneticsBioinformaticsGenetic AdmixtureMedicine
Genomic relationship matrices derived from animal genotypes enable prediction of EBVs via BLUP, yet conventional accuracy estimates are inflated by sampling errors in the matrix elements. The study proposes a deterministic approach to forecast genomic EBV accuracy prior to collecting individual animal data. The method estimates the proportion of genetic variance explained by markers and the accuracy of marker effect estimation based on pairwise relationship variance (mean linkage disequilibrium), and is validated with simulations and Holstein milk‑fat data. Regressing the genomic relationship matrix toward the pedigree matrix yields unbiased accuracy estimates, which rise with the number of markers as the regression coefficient grows.
Estimated breeding values (EBVs) using data from genetic markers can be predicted using a genomic relationship matrix, derived from animal's genotypes, and best linear unbiased prediction. However, if the accuracy of the EBVs is calculated in the usual manner (from the inverse element of the coefficient matrix), it is likely to be overestimated owing to sampling errors in elements of the genomic relationship matrix. We show here that the correct accuracy can be obtained by regressing the relationship matrix towards the pedigree relationship matrix so that it is an unbiased estimate of the relationships at the QTL controlling the trait. This method shows how the accuracy increases as the number of markers used increases because the regression coefficient (of genomic relationship towards pedigree relationship) increases. We also present a deterministic method for predicting the accuracy of such genomic EBVs before data on individual animals are collected. This method estimates the proportion of genetic variance explained by the markers, which is equal to the regression coefficient described above, and the accuracy with which marker effects are estimated. The latter depends on the variance in relationship between pairs of animals, which equals the mean linkage disequilibrium over all pairs of loci. The theory was validated using simulated data and data on fat concentration in the milk of Holstein cattle.
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