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Sample size determination for training set optimization in genomic prediction
KEY MESSAGE: A practical approach is developed to determine a cost-effective optimal training set for selective phenotyping in a genomic prediction study. An R function is provided to facilitate the application of the approach. ABSTRACT: Genomic prediction (GP) is a statistical method used to select...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011335/ https://www.ncbi.nlm.nih.gov/pubmed/36912999 http://dx.doi.org/10.1007/s00122-023-04254-9 |
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author | Wu, Po-Ya Ou, Jen-Hsiang Liao, Chen-Tuo |
author_facet | Wu, Po-Ya Ou, Jen-Hsiang Liao, Chen-Tuo |
author_sort | Wu, Po-Ya |
collection | PubMed |
description | KEY MESSAGE: A practical approach is developed to determine a cost-effective optimal training set for selective phenotyping in a genomic prediction study. An R function is provided to facilitate the application of the approach. ABSTRACT: Genomic prediction (GP) is a statistical method used to select quantitative traits in animal or plant breeding. For this purpose, a statistical prediction model is first built that uses phenotypic and genotypic data in a training set. The trained model is then used to predict genomic estimated breeding values (GEBVs) for individuals within a breeding population. Setting the sample size of the training set usually takes into account time and space constraints that are inevitable in an agricultural experiment. However, the determination of the sample size remains an unresolved issue for a GP study. By applying the logistic growth curve to identify prediction accuracy for the GEBVs and the training set size, a practical approach was developed to determine a cost-effective optimal training set for a given genome dataset with known genotypic data. Three real genome datasets were used to illustrate the proposed approach. An R function is provided to facilitate widespread application of this approach to sample size determination, which can help breeders to identify a set of genotypes with an economical sample size for selective phenotyping. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-023-04254-9. |
format | Online Article Text |
id | pubmed-10011335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100113352023-03-15 Sample size determination for training set optimization in genomic prediction Wu, Po-Ya Ou, Jen-Hsiang Liao, Chen-Tuo Theor Appl Genet Original Article KEY MESSAGE: A practical approach is developed to determine a cost-effective optimal training set for selective phenotyping in a genomic prediction study. An R function is provided to facilitate the application of the approach. ABSTRACT: Genomic prediction (GP) is a statistical method used to select quantitative traits in animal or plant breeding. For this purpose, a statistical prediction model is first built that uses phenotypic and genotypic data in a training set. The trained model is then used to predict genomic estimated breeding values (GEBVs) for individuals within a breeding population. Setting the sample size of the training set usually takes into account time and space constraints that are inevitable in an agricultural experiment. However, the determination of the sample size remains an unresolved issue for a GP study. By applying the logistic growth curve to identify prediction accuracy for the GEBVs and the training set size, a practical approach was developed to determine a cost-effective optimal training set for a given genome dataset with known genotypic data. Three real genome datasets were used to illustrate the proposed approach. An R function is provided to facilitate widespread application of this approach to sample size determination, which can help breeders to identify a set of genotypes with an economical sample size for selective phenotyping. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-023-04254-9. Springer Berlin Heidelberg 2023-03-13 2023 /pmc/articles/PMC10011335/ /pubmed/36912999 http://dx.doi.org/10.1007/s00122-023-04254-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Wu, Po-Ya Ou, Jen-Hsiang Liao, Chen-Tuo Sample size determination for training set optimization in genomic prediction |
title | Sample size determination for training set optimization in genomic prediction |
title_full | Sample size determination for training set optimization in genomic prediction |
title_fullStr | Sample size determination for training set optimization in genomic prediction |
title_full_unstemmed | Sample size determination for training set optimization in genomic prediction |
title_short | Sample size determination for training set optimization in genomic prediction |
title_sort | sample size determination for training set optimization in genomic prediction |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10011335/ https://www.ncbi.nlm.nih.gov/pubmed/36912999 http://dx.doi.org/10.1007/s00122-023-04254-9 |
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