Comparing Genomic Prediction Models by Means of Cross Validation

In the two decades of continuous development of genomic selection, a great variety of models have been proposed to make predictions from the information available in dense marker panels. Besides deciding which particular model to use, practitioners also need to make many minor choices for those para...

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Autores principales: Matías F. Schrauf, Gustavo de los Campos, Sebastián Munilla
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Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/d8bb4b08605549eeb8fc88dc3c3b7037
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spelling oai:doaj.org-article:d8bb4b08605549eeb8fc88dc3c3b70372021-11-19T04:52:45ZComparing Genomic Prediction Models by Means of Cross Validation1664-462X10.3389/fpls.2021.734512https://doaj.org/article/d8bb4b08605549eeb8fc88dc3c3b70372021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fpls.2021.734512/fullhttps://doaj.org/toc/1664-462XIn the two decades of continuous development of genomic selection, a great variety of models have been proposed to make predictions from the information available in dense marker panels. Besides deciding which particular model to use, practitioners also need to make many minor choices for those parameters in the model which are not typically estimated by the data (so called “hyper-parameters”). When the focus is placed on predictions, most of these decisions are made in a direction sought to optimize predictive accuracy. Here we discuss and illustrate using publicly available crop datasets the use of cross validation to make many such decisions. In particular, we emphasize the importance of paired comparisons to achieve high power in the comparison between candidate models, as well as the need to define notions of relevance in the difference between their performances. Regarding the latter, we borrow the idea of equivalence margins from clinical research and introduce new statistical tests. We conclude that most hyper-parameters can be learnt from the data by either minimizing REML or by using weakly-informative priors, with good predictive results. In particular, the default options in a popular software are generally competitive with the optimal values. With regard to the performance assessments themselves, we conclude that the paired k-fold cross validation is a generally applicable and statistically powerful methodology to assess differences in model accuracies. Coupled with the definition of equivalence margins based on expected genetic gain, it becomes a useful tool for breeders.Matías F. SchraufMatías F. SchraufGustavo de los CamposSebastián MunillaSebastián MunillaFrontiers Media S.A.articlegenomic selectioncross validationplant breedinggenomic modelsmodel selectionPlant cultureSB1-1110ENFrontiers in Plant Science, Vol 12 (2021)
institution DOAJ
collection DOAJ
language EN
topic genomic selection
cross validation
plant breeding
genomic models
model selection
Plant culture
SB1-1110
spellingShingle genomic selection
cross validation
plant breeding
genomic models
model selection
Plant culture
SB1-1110
Matías F. Schrauf
Matías F. Schrauf
Gustavo de los Campos
Sebastián Munilla
Sebastián Munilla
Comparing Genomic Prediction Models by Means of Cross Validation
description In the two decades of continuous development of genomic selection, a great variety of models have been proposed to make predictions from the information available in dense marker panels. Besides deciding which particular model to use, practitioners also need to make many minor choices for those parameters in the model which are not typically estimated by the data (so called “hyper-parameters”). When the focus is placed on predictions, most of these decisions are made in a direction sought to optimize predictive accuracy. Here we discuss and illustrate using publicly available crop datasets the use of cross validation to make many such decisions. In particular, we emphasize the importance of paired comparisons to achieve high power in the comparison between candidate models, as well as the need to define notions of relevance in the difference between their performances. Regarding the latter, we borrow the idea of equivalence margins from clinical research and introduce new statistical tests. We conclude that most hyper-parameters can be learnt from the data by either minimizing REML or by using weakly-informative priors, with good predictive results. In particular, the default options in a popular software are generally competitive with the optimal values. With regard to the performance assessments themselves, we conclude that the paired k-fold cross validation is a generally applicable and statistically powerful methodology to assess differences in model accuracies. Coupled with the definition of equivalence margins based on expected genetic gain, it becomes a useful tool for breeders.
format article
author Matías F. Schrauf
Matías F. Schrauf
Gustavo de los Campos
Sebastián Munilla
Sebastián Munilla
author_facet Matías F. Schrauf
Matías F. Schrauf
Gustavo de los Campos
Sebastián Munilla
Sebastián Munilla
author_sort Matías F. Schrauf
title Comparing Genomic Prediction Models by Means of Cross Validation
title_short Comparing Genomic Prediction Models by Means of Cross Validation
title_full Comparing Genomic Prediction Models by Means of Cross Validation
title_fullStr Comparing Genomic Prediction Models by Means of Cross Validation
title_full_unstemmed Comparing Genomic Prediction Models by Means of Cross Validation
title_sort comparing genomic prediction models by means of cross validation
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/d8bb4b08605549eeb8fc88dc3c3b7037
work_keys_str_mv AT matiasfschrauf comparinggenomicpredictionmodelsbymeansofcrossvalidation
AT matiasfschrauf comparinggenomicpredictionmodelsbymeansofcrossvalidation
AT gustavodeloscampos comparinggenomicpredictionmodelsbymeansofcrossvalidation
AT sebastianmunilla comparinggenomicpredictionmodelsbymeansofcrossvalidation
AT sebastianmunilla comparinggenomicpredictionmodelsbymeansofcrossvalidation
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