| Literature DB >> 32474602 |
Anderson Antonio Carvalho Alves1, Rebeka Magalhães da Costa1, Tiago Bresolin2, Gerardo Alves Fernandes Júnior1, Rafael Espigolan3, André Mauric Frossard Ribeiro4, Roberto Carvalheiro1,4, Lucia Galvão de Albuquerque1,4.
Abstract
The aim of this study was to compare the predictive performance of the Genomic Best Linear Unbiased Predictor (GBLUP) and machine learning methods (Random Forest, RF; Support Vector Machine, SVM; Artificial Neural Network, ANN) in simulated populations presenting different levels of dominance effects. Simulated genome comprised 50k SNP and 300 QTL, both biallelic and randomly distributed across 29 autosomes. A total of six traits were simulated considering different values for the narrow and broad-sense heritability. In the purely additive scenario with low heritability (h2 = 0.10), the predictive ability obtained using GBLUP was slightly higher than the other methods whereas ANN provided the highest accuracies for scenarios with moderate heritability (h2 = 0.30). The accuracies of dominance deviations predictions varied from 0.180 to 0.350 in GBLUP extended for dominance effects (GBLUP-D), from 0.06 to 0.185 in RF and they were null using the ANN and SVM methods. Although RF has presented higher accuracies for total genetic effect predictions, the mean-squared error values in such a model were worse than those observed for GBLUP-D in scenarios with large additive and dominance variances. When applied to prescreen important regions, the RF approach detected QTL with high additive and/or dominance effects. Among machine learning methods, only the RF was capable to cover implicitly dominance effects without increasing the number of covariates in the model, resulting in higher accuracies for the total genetic and phenotypic values as the dominance ratio increases. Nevertheless, whether the interest is to infer directly on dominance effects, GBLUP-D could be a more suitable method.Entities:
Keywords: Artificial Neural Network; Random Forest; Support Vector Machine; genomic selection; nonadditive effects
Mesh:
Year: 2020 PMID: 32474602 PMCID: PMC7367166 DOI: 10.1093/jas/skaa179
Source DB: PubMed Journal: J Anim Sci ISSN: 0021-8812 Impact factor: 3.159