Accuracy of breeding values of 'unrelated' individuals predicted by dense SNP genotyping

Abstract

Background: Recent developments in SNP discovery and high throughput genotyping technology have made the use of high-density SNP markers to predict breeding values feasible. This involves estimation of the SNP effects in a training data set, and use of these estimates to evaluate the breeding values of other 'evaluation' individuals. Simulation studies have shown that these predictions of breeding values can be accurate, when training and evaluation individuals are (closely) related. However, many general applications of genomic selection require the prediction of breeding values of 'unrelated' individuals, i.e. individuals from the same population, but not particularly closely related to the training individuals. Methods. Accuracy of selection was investigated by computer simulation of small populations. Using scaling arguments, the results were extended to different populations, training data sets and genome sizes, and different trait heritabilities. Results. Prediction of breeding values of unrelated individuals required a substantially higher marker density and number of training records than when prediction individuals were offspring of training individuals. However, when the number of records was 2*N e*L and the number of markers was 10*N e*L, the breeding values of unrelated individuals could be predicted with accuracies of 0.88 - 0.93, where Neis the effective population size and L the genome size in Morgan. Reducing this requirement to 1*Ne*L individuals, reduced prediction accuracies to 0.73-0.83. Conclusion. For livestock populations, 1NeL requires about ∼30,000 training records, but this may be reduced if training and evaluation animals are related. A prediction equation is presented, that predicts accuracy when training and evaluation individuals are related. For humans, 1NeL requires ∼350,000 individuals, which means that human disease risk prediction is possible only for diseases that are determined by a limited number of genes. Otherwise, genotyping and phenotypic recording need to become very common in the future. © 2009 Meuwissen.