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Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction

Training set size is an important determinant of genomic prediction accuracy. Plant breeding programs are characterized by a high degree of structuring, particularly into populations. This hampers the establishment of large training sets for each population. Pooling populations increases training se...

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Autores principales: Technow, Frank, Totir, L. Radu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528317/
https://www.ncbi.nlm.nih.gov/pubmed/26024866
http://dx.doi.org/10.1534/g3.115.019299
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author Technow, Frank
Totir, L. Radu
author_facet Technow, Frank
Totir, L. Radu
author_sort Technow, Frank
collection PubMed
description Training set size is an important determinant of genomic prediction accuracy. Plant breeding programs are characterized by a high degree of structuring, particularly into populations. This hampers the establishment of large training sets for each population. Pooling populations increases training set size but ignores unique genetic characteristics of each. A possible solution is partial pooling with multilevel models, which allows estimating population-specific marker effects while still leveraging information across populations. We developed a Bayesian multilevel whole-genome regression model and compared its performance with that of the popular BayesA model applied to each population separately (no pooling) and to the joined data set (complete pooling). As an example, we analyzed a wide array of traits from the nested association mapping maize population. There we show that for small population sizes (e.g., <50), partial pooling increased prediction accuracy over no or complete pooling for populations represented in the training set. No pooling was superior; however, when populations were large. In another example data set of interconnected biparental maize populations either partial or complete pooling was superior, depending on the trait. A simulation showed that no pooling is superior when differences in genetic effects among populations are large and partial pooling when they are intermediate. With small differences, partial and complete pooling achieved equally high accuracy. For prediction of new populations, partial and complete pooling had very similar accuracy in all cases. We conclude that partial pooling with multilevel models can maximize the potential of pooling by making optimal use of information in pooled training sets.
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spelling pubmed-45283172015-08-10 Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction Technow, Frank Totir, L. Radu G3 (Bethesda) Genomic Selection Training set size is an important determinant of genomic prediction accuracy. Plant breeding programs are characterized by a high degree of structuring, particularly into populations. This hampers the establishment of large training sets for each population. Pooling populations increases training set size but ignores unique genetic characteristics of each. A possible solution is partial pooling with multilevel models, which allows estimating population-specific marker effects while still leveraging information across populations. We developed a Bayesian multilevel whole-genome regression model and compared its performance with that of the popular BayesA model applied to each population separately (no pooling) and to the joined data set (complete pooling). As an example, we analyzed a wide array of traits from the nested association mapping maize population. There we show that for small population sizes (e.g., <50), partial pooling increased prediction accuracy over no or complete pooling for populations represented in the training set. No pooling was superior; however, when populations were large. In another example data set of interconnected biparental maize populations either partial or complete pooling was superior, depending on the trait. A simulation showed that no pooling is superior when differences in genetic effects among populations are large and partial pooling when they are intermediate. With small differences, partial and complete pooling achieved equally high accuracy. For prediction of new populations, partial and complete pooling had very similar accuracy in all cases. We conclude that partial pooling with multilevel models can maximize the potential of pooling by making optimal use of information in pooled training sets. Genetics Society of America 2015-05-29 /pmc/articles/PMC4528317/ /pubmed/26024866 http://dx.doi.org/10.1534/g3.115.019299 Text en Copyright © 2015 Technow and Totir 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
Technow, Frank
Totir, L. Radu
Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction
title Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction
title_full Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction
title_fullStr Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction
title_full_unstemmed Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction
title_short Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction
title_sort using bayesian multilevel whole genome regression models for partial pooling of training sets in genomic prediction
topic Genomic Selection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528317/
https://www.ncbi.nlm.nih.gov/pubmed/26024866
http://dx.doi.org/10.1534/g3.115.019299
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