Abstract
BackgroundIn genomic prediction, an important measure of accuracy is the correlation between the predicted and the true breeding values. Direct computation of this quantity for real datasets is not possible, because the true breeding value is unknown. Instead, the correlation between the predicted breeding values and the observed phenotypic values, called predictive ability, is often computed. In order to indirectly estimate predictive accuracy, this latter correlation is usually divided by an estimate of the square root of heritability. In this study we use simulation to evaluate estimates of predictive accuracy for seven methods, four (1 to 4) of which use an estimate of heritability to divide predictive ability computed by cross-validation. Between them the seven methods cover balanced and unbalanced datasets as well as correlated and uncorrelated genotypes. We propose one new indirect method (4) and two direct methods (5 and 6) for estimating predictive accuracy and compare their performances and those of four other existing approaches (three indirect (1 to 3) and one direct (7)) with simulated true predictive accuracy as the benchmark and with each other.ResultsThe size of the estimated genetic variance and hence heritability exerted the strongest influence on the variation in the estimated predictive accuracy. Increasing the number of genotypes considerably increases the time required to compute predictive accuracy by all the seven methods, most notably for the five methods that require cross-validation (Methods 1, 2, 3, 4 and 6). A new method that we propose (Method 5) and an existing method (Method 7) used in animal breeding programs were the fastest and gave the least biased, most precise and stable estimates of predictive accuracy. Of the methods that use cross-validation Methods 4 and 6 were often the best.ConclusionsThe estimated genetic variance and the number of genotypes had the greatest influence on predictive accuracy. Methods 5 and 7 were the fastest and produced the least biased, the most precise, robust and stable estimates of predictive accuracy. These properties argue for routinely using Methods 5 and 7 to assess predictive accuracy in genomic selection studies.
Highlights
In genomic prediction, an important measure of accuracy is the correlation between the predicted and the true breeding values
M0 is the square of the true correlation between the predicted and the true simulated breeding values used as the benchmark for assessing the estimated heritability. †mean squared deviation (MSD)=Mean squared deviation and H2 = 0 is the number of datasets for which the estimated heritability was zero. *The number of the equation used in the text is in parenthesis
Across scenarios based on the same data set, the estimated heritability tended to be closer to its true value in Scenario 1 than in 2 and in Scenario 3 than in 4 (Table 5), implying that reducing the genetic variance by a factor of 10 in scenarios 2 and 4 reduced the accuracy of estimated heritability
Summary
An important measure of accuracy is the correlation between the predicted and the true breeding values. Direct computation of this quantity for real datasets is not possible, because the true breeding value is unknown. In this study we use simulation to evaluate estimates of predictive accuracy for seven methods, four (1 to 4) of which use an estimate of heritability to divide predictive ability computed by cross-validation. Genomic selection (GS) is a method for predicting genomic breeding values using molecular markers covering the whole genome [1,2,3]. Accurate evaluation of the performance of genomic selection is difficult in practice because true breeding values are typically unknown. We use simulated true breeding values to directly compute the true correlation (accuracy) between
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