In genomewide selection, the expected correlation between predicted performance and true genotypic value is a function of the training population size ( N ), heritability on an entry‐mean basis ( h 2 ), and effective number of chromosome segments underlying the trait ( M e ). Our objectives were to (i) determine how the prediction accuracy of different traits responds to changes in N , h 2 , and number of markers ( N M ) and (ii) determine if prediction accuracy is equal across traits if N , h 2 , and N M are kept constant. In a simulated population and four empirical populations in maize ( Zea mays L.), barley ( Hordeum vulgare L.), and wheat ( Triticum aestivum L.), we added random nongenetic effects to the phenotypic data to reduce h 2 to 0.50, 0.30 and 0.20. As expected, increasing N , h 2 , and N M increased prediction accuracy. For the same trait within the same population, prediction accuracy was constant for different combinations of N and h 2 that led to the same Nh 2 . Different traits, however, varied in their prediction accuracy even when N , h 2 , and N M were constant. Yield traits had lower prediction accuracy than other traits despite the constant N , h 2 , and N M . Empirical evidence and experience on the predictability of different traits are needed in designing training populations.
No takes yet. Share an insight, caveat, or question.
Combs et al. (2013) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: