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A Bayesian Decision Theory Approach for Genomic Selection

Plant and animal breeders are interested in selecting the best individuals from a candidate set for the next breeding cycle. In this paper, we propose a formal method under the Bayesian decision theory framework to tackle the selection problem based on genomic selection (GS) in single- and multi-tra...

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Autores principales: Villar-Hernández, Bartolo de Jesús, Pérez-Elizalde, Sergio, Crossa, José, Pérez-Rodríguez, Paulino, Toledo, Fernando H., Burgueño, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118314/
https://www.ncbi.nlm.nih.gov/pubmed/30021830
http://dx.doi.org/10.1534/g3.118.200430
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author Villar-Hernández, Bartolo de Jesús
Pérez-Elizalde, Sergio
Crossa, José
Pérez-Rodríguez, Paulino
Toledo, Fernando H.
Burgueño, Juan
author_facet Villar-Hernández, Bartolo de Jesús
Pérez-Elizalde, Sergio
Crossa, José
Pérez-Rodríguez, Paulino
Toledo, Fernando H.
Burgueño, Juan
author_sort Villar-Hernández, Bartolo de Jesús
collection PubMed
description Plant and animal breeders are interested in selecting the best individuals from a candidate set for the next breeding cycle. In this paper, we propose a formal method under the Bayesian decision theory framework to tackle the selection problem based on genomic selection (GS) in single- and multi-trait settings. We proposed and tested three univariate loss functions (Kullback-Leibler, KL; Continuous Ranked Probability Score, CRPS; Linear-Linear loss, LinLin) and their corresponding multivariate generalizations (Kullback-Leibler, KL; Energy Score, EnergyS; and the Multivariate Asymmetric Loss Function, MALF). We derived and expressed all the loss functions in terms of heritability and tested them on a real wheat dataset for one cycle of selection and in a simulated selection program. The performance of each univariate loss function was compared with the standard method of selection (Std) that does not use loss functions. We compared the performance in terms of the selection response and the decrease in the population’s genetic variance during recurrent breeding cycles. Results suggest that it is possible to obtain better performance in a long-term breeding program using the single-trait scheme by selecting 30% of the best individuals in each cycle but not by selecting 10% of the best individuals. For the multi-trait approach, results show that the population mean for all traits under consideration had positive gains, even though two of the traits were negatively correlated. The corresponding population variances were not statistically different from the different loss function during the 10(th) selection cycle. Using the loss function should be a useful criterion when selecting the candidates for selection for the next breeding cycle.
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spelling pubmed-61183142018-09-04 A Bayesian Decision Theory Approach for Genomic Selection Villar-Hernández, Bartolo de Jesús Pérez-Elizalde, Sergio Crossa, José Pérez-Rodríguez, Paulino Toledo, Fernando H. Burgueño, Juan G3 (Bethesda) Genomic Selection Plant and animal breeders are interested in selecting the best individuals from a candidate set for the next breeding cycle. In this paper, we propose a formal method under the Bayesian decision theory framework to tackle the selection problem based on genomic selection (GS) in single- and multi-trait settings. We proposed and tested three univariate loss functions (Kullback-Leibler, KL; Continuous Ranked Probability Score, CRPS; Linear-Linear loss, LinLin) and their corresponding multivariate generalizations (Kullback-Leibler, KL; Energy Score, EnergyS; and the Multivariate Asymmetric Loss Function, MALF). We derived and expressed all the loss functions in terms of heritability and tested them on a real wheat dataset for one cycle of selection and in a simulated selection program. The performance of each univariate loss function was compared with the standard method of selection (Std) that does not use loss functions. We compared the performance in terms of the selection response and the decrease in the population’s genetic variance during recurrent breeding cycles. Results suggest that it is possible to obtain better performance in a long-term breeding program using the single-trait scheme by selecting 30% of the best individuals in each cycle but not by selecting 10% of the best individuals. For the multi-trait approach, results show that the population mean for all traits under consideration had positive gains, even though two of the traits were negatively correlated. The corresponding population variances were not statistically different from the different loss function during the 10(th) selection cycle. Using the loss function should be a useful criterion when selecting the candidates for selection for the next breeding cycle. Genetics Society of America 2018-07-18 /pmc/articles/PMC6118314/ /pubmed/30021830 http://dx.doi.org/10.1534/g3.118.200430 Text en Copyright © 2018 Villar-Hernández et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomic Selection
Villar-Hernández, Bartolo de Jesús
Pérez-Elizalde, Sergio
Crossa, José
Pérez-Rodríguez, Paulino
Toledo, Fernando H.
Burgueño, Juan
A Bayesian Decision Theory Approach for Genomic Selection
title A Bayesian Decision Theory Approach for Genomic Selection
title_full A Bayesian Decision Theory Approach for Genomic Selection
title_fullStr A Bayesian Decision Theory Approach for Genomic Selection
title_full_unstemmed A Bayesian Decision Theory Approach for Genomic Selection
title_short A Bayesian Decision Theory Approach for Genomic Selection
title_sort bayesian decision theory approach for genomic selection
topic Genomic Selection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6118314/
https://www.ncbi.nlm.nih.gov/pubmed/30021830
http://dx.doi.org/10.1534/g3.118.200430
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