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Optimization of multi-environment trials for genomic selection based on crop models

KEY MESSAGE: We propose a statistical criterion to optimize multi-environment trials to predict genotype × environment interactions more efficiently, by combining crop growth models and genomic selection models. ABSTRACT: Genotype × environment interactions (GEI) are common in plant multi-environmen...

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Autores principales: Rincent, R., Kuhn, E., Monod, H., Oury, F.-X., Rousset, M., Allard, V., Le Gouis, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511605/
https://www.ncbi.nlm.nih.gov/pubmed/28540573
http://dx.doi.org/10.1007/s00122-017-2922-4
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author Rincent, R.
Kuhn, E.
Monod, H.
Oury, F.-X.
Rousset, M.
Allard, V.
Le Gouis, J.
author_facet Rincent, R.
Kuhn, E.
Monod, H.
Oury, F.-X.
Rousset, M.
Allard, V.
Le Gouis, J.
author_sort Rincent, R.
collection PubMed
description KEY MESSAGE: We propose a statistical criterion to optimize multi-environment trials to predict genotype × environment interactions more efficiently, by combining crop growth models and genomic selection models. ABSTRACT: Genotype × environment interactions (GEI) are common in plant multi-environment trials (METs). In this context, models developed for genomic selection (GS) that refers to the use of genome-wide information for predicting breeding values of selection candidates need to be adapted. One promising way to increase prediction accuracy in various environments is to combine ecophysiological and genetic modelling thanks to crop growth models (CGM) incorporating genetic parameters. The efficiency of this approach relies on the quality of the parameter estimates, which depends on the environments composing this MET used for calibration. The objective of this study was to determine a method to optimize the set of environments composing the MET for estimating genetic parameters in this context. A criterion called OptiMET was defined to this aim, and was evaluated on simulated and real data, with the example of wheat phenology. The MET defined with OptiMET allowed estimating the genetic parameters with lower error, leading to higher QTL detection power and higher prediction accuracies. MET defined with OptiMET was on average more efficient than random MET composed of twice as many environments, in terms of quality of the parameter estimates. OptiMET is thus a valuable tool to determine optimal experimental conditions to best exploit MET and the phenotyping tools that are currently developed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-017-2922-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-55116052017-07-31 Optimization of multi-environment trials for genomic selection based on crop models Rincent, R. Kuhn, E. Monod, H. Oury, F.-X. Rousset, M. Allard, V. Le Gouis, J. Theor Appl Genet Original Article KEY MESSAGE: We propose a statistical criterion to optimize multi-environment trials to predict genotype × environment interactions more efficiently, by combining crop growth models and genomic selection models. ABSTRACT: Genotype × environment interactions (GEI) are common in plant multi-environment trials (METs). In this context, models developed for genomic selection (GS) that refers to the use of genome-wide information for predicting breeding values of selection candidates need to be adapted. One promising way to increase prediction accuracy in various environments is to combine ecophysiological and genetic modelling thanks to crop growth models (CGM) incorporating genetic parameters. The efficiency of this approach relies on the quality of the parameter estimates, which depends on the environments composing this MET used for calibration. The objective of this study was to determine a method to optimize the set of environments composing the MET for estimating genetic parameters in this context. A criterion called OptiMET was defined to this aim, and was evaluated on simulated and real data, with the example of wheat phenology. The MET defined with OptiMET allowed estimating the genetic parameters with lower error, leading to higher QTL detection power and higher prediction accuracies. MET defined with OptiMET was on average more efficient than random MET composed of twice as many environments, in terms of quality of the parameter estimates. OptiMET is thus a valuable tool to determine optimal experimental conditions to best exploit MET and the phenotyping tools that are currently developed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-017-2922-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-05-24 2017 /pmc/articles/PMC5511605/ /pubmed/28540573 http://dx.doi.org/10.1007/s00122-017-2922-4 Text en © The Author(s) 2017 Open AccessThis article is 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 you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Rincent, R.
Kuhn, E.
Monod, H.
Oury, F.-X.
Rousset, M.
Allard, V.
Le Gouis, J.
Optimization of multi-environment trials for genomic selection based on crop models
title Optimization of multi-environment trials for genomic selection based on crop models
title_full Optimization of multi-environment trials for genomic selection based on crop models
title_fullStr Optimization of multi-environment trials for genomic selection based on crop models
title_full_unstemmed Optimization of multi-environment trials for genomic selection based on crop models
title_short Optimization of multi-environment trials for genomic selection based on crop models
title_sort optimization of multi-environment trials for genomic selection based on crop models
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511605/
https://www.ncbi.nlm.nih.gov/pubmed/28540573
http://dx.doi.org/10.1007/s00122-017-2922-4
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