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Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments
KEY MESSAGE: The accuracy of genomic prediction of phenotypes can be increased by including the top-ranked pairwise SNP interactions into the prediction model. ABSTRACT: We compared the predictive ability of various prediction models for a maize dataset derived from 910 doubled haploid lines from tw...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354961/ https://www.ncbi.nlm.nih.gov/pubmed/34115154 http://dx.doi.org/10.1007/s00122-021-03868-1 |
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author | Vojgani, Elaheh Pook, Torsten Martini, Johannes W. R. Hölker, Armin C. Mayer, Manfred Schön, Chris-Carolin Simianer, Henner |
author_facet | Vojgani, Elaheh Pook, Torsten Martini, Johannes W. R. Hölker, Armin C. Mayer, Manfred Schön, Chris-Carolin Simianer, Henner |
author_sort | Vojgani, Elaheh |
collection | PubMed |
description | KEY MESSAGE: The accuracy of genomic prediction of phenotypes can be increased by including the top-ranked pairwise SNP interactions into the prediction model. ABSTRACT: We compared the predictive ability of various prediction models for a maize dataset derived from 910 doubled haploid lines from two European landraces (Kemater Landmais Gelb and Petkuser Ferdinand Rot), which were tested at six locations in Germany and Spain. The compared models were Genomic Best Linear Unbiased Prediction (GBLUP) as an additive model, Epistatic Random Regression BLUP (ERRBLUP) accounting for all pairwise SNP interactions, and selective Epistatic Random Regression BLUP (sERRBLUP) accounting for a selected subset of pairwise SNP interactions. These models have been compared in both univariate and bivariate statistical settings for predictions within and across environments. Our results indicate that modeling all pairwise SNP interactions into the univariate/bivariate model (ERRBLUP) is not superior in predictive ability to the respective additive model (GBLUP). However, incorporating only a selected subset of interactions with the highest effect variances in univariate/bivariate sERRBLUP can increase predictive ability significantly compared to the univariate/bivariate GBLUP. Overall, bivariate models consistently outperform univariate models in predictive ability. Across all studied traits, locations and landraces, the increase in prediction accuracy from univariate GBLUP to univariate sERRBLUP ranged from 5.9 to 112.4 percent, with an average increase of 47 percent. For bivariate models, the change ranged from −0.3 to + 27.9 percent comparing the bivariate sERRBLUP to the bivariate GBLUP, with an average increase of 11 percent. This considerable increase in predictive ability achieved by sERRBLUP may be of interest for “sparse testing” approaches in which only a subset of the lines/hybrids of interest is observed at each location. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-021-03868-1. |
format | Online Article Text |
id | pubmed-8354961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-83549612021-08-25 Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments Vojgani, Elaheh Pook, Torsten Martini, Johannes W. R. Hölker, Armin C. Mayer, Manfred Schön, Chris-Carolin Simianer, Henner Theor Appl Genet Original Article KEY MESSAGE: The accuracy of genomic prediction of phenotypes can be increased by including the top-ranked pairwise SNP interactions into the prediction model. ABSTRACT: We compared the predictive ability of various prediction models for a maize dataset derived from 910 doubled haploid lines from two European landraces (Kemater Landmais Gelb and Petkuser Ferdinand Rot), which were tested at six locations in Germany and Spain. The compared models were Genomic Best Linear Unbiased Prediction (GBLUP) as an additive model, Epistatic Random Regression BLUP (ERRBLUP) accounting for all pairwise SNP interactions, and selective Epistatic Random Regression BLUP (sERRBLUP) accounting for a selected subset of pairwise SNP interactions. These models have been compared in both univariate and bivariate statistical settings for predictions within and across environments. Our results indicate that modeling all pairwise SNP interactions into the univariate/bivariate model (ERRBLUP) is not superior in predictive ability to the respective additive model (GBLUP). However, incorporating only a selected subset of interactions with the highest effect variances in univariate/bivariate sERRBLUP can increase predictive ability significantly compared to the univariate/bivariate GBLUP. Overall, bivariate models consistently outperform univariate models in predictive ability. Across all studied traits, locations and landraces, the increase in prediction accuracy from univariate GBLUP to univariate sERRBLUP ranged from 5.9 to 112.4 percent, with an average increase of 47 percent. For bivariate models, the change ranged from −0.3 to + 27.9 percent comparing the bivariate sERRBLUP to the bivariate GBLUP, with an average increase of 11 percent. This considerable increase in predictive ability achieved by sERRBLUP may be of interest for “sparse testing” approaches in which only a subset of the lines/hybrids of interest is observed at each location. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00122-021-03868-1. Springer Berlin Heidelberg 2021-06-11 2021 /pmc/articles/PMC8354961/ /pubmed/34115154 http://dx.doi.org/10.1007/s00122-021-03868-1 Text en © The Author(s) 2021 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 Vojgani, Elaheh Pook, Torsten Martini, Johannes W. R. Hölker, Armin C. Mayer, Manfred Schön, Chris-Carolin Simianer, Henner Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments |
title | Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments |
title_full | Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments |
title_fullStr | Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments |
title_full_unstemmed | Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments |
title_short | Accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments |
title_sort | accounting for epistasis improves genomic prediction of phenotypes with univariate and bivariate models across environments |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354961/ https://www.ncbi.nlm.nih.gov/pubmed/34115154 http://dx.doi.org/10.1007/s00122-021-03868-1 |
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