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Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions
BACKGROUND: Accurate evaluation of SNP effects is important for genome wide association studies and for genomic prediction. The genetic architecture of quantitative traits differs widely, with some traits exhibiting few if any quantitative trait loci (QTL) with large effects, while other traits have...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750167/ https://www.ncbi.nlm.nih.gov/pubmed/26870325 http://dx.doi.org/10.1186/s40104-016-0066-z |
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author | Wolc, Anna Arango, Jesus Settar, Petek Fulton, Janet E. O’Sullivan, Neil P. Dekkers, Jack C. M. Fernando, Rohan Garrick, Dorian J. |
author_facet | Wolc, Anna Arango, Jesus Settar, Petek Fulton, Janet E. O’Sullivan, Neil P. Dekkers, Jack C. M. Fernando, Rohan Garrick, Dorian J. |
author_sort | Wolc, Anna |
collection | PubMed |
description | BACKGROUND: Accurate evaluation of SNP effects is important for genome wide association studies and for genomic prediction. The genetic architecture of quantitative traits differs widely, with some traits exhibiting few if any quantitative trait loci (QTL) with large effects, while other traits have one or several easily detectable QTL with large effects. METHODS: Body weight in broilers and egg weight in layers are two examples of traits that have QTL of large effect. A commonly used method for genome wide association studies is to fit a mixture model such as BayesB that assumes some known proportion of SNP effects are zero. In contrast, the most commonly used method for genomic prediction is known as GBLUP, which involves fitting an animal model to phenotypic data with the variance-covariance or genomic relationship matrix among the animals being determined by genome wide SNP genotypes. Genotypes at each SNP are typically weighted equally in determining the genomic relationship matrix for GBLUP. We used the equivalent marker effects model formulation of GBLUP for this study. We compare these two classes of models using egg weight data collected over 8 generations from 2,324 animals genotyped with a 42 K SNP panel. RESULTS: Using data from the first 7 generations, both BayesB and GBLUP found the largest QTL in a similar well-recognized QTL region, but this QTL was estimated to account for 24 % of genetic variation with BayesB and less than 1 % with GBLUP. When predicting phenotypes in generation 8 BayesB accounted for 36 % of the phenotypic variation and GBLUP for 25 %. When using only data from any one generation, the same QTL was identified with BayesB in all but one generation but never with GBLUP. Predictions of phenotypes in generations 2 to 7 based on only 295 animals from generation 1 accounted for 10 % phenotypic variation with BayesB but only 6 % with GBLUP. Predicting phenotype using only the marker effects in the 1 Mb region that accounted for the largest effect on egg weight from generation 1 data alone accounted for almost 8 % variation using BayesB but had no predictive power with GBLUP. CONCLUSIONS: In conclusion, In the presence of large effect QTL, BayesB did a better job of QTL detection and its genomic predictions were more accurate and persistent than those from GBLUP. |
format | Online Article Text |
id | pubmed-4750167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47501672016-02-12 Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions Wolc, Anna Arango, Jesus Settar, Petek Fulton, Janet E. O’Sullivan, Neil P. Dekkers, Jack C. M. Fernando, Rohan Garrick, Dorian J. J Anim Sci Biotechnol Research BACKGROUND: Accurate evaluation of SNP effects is important for genome wide association studies and for genomic prediction. The genetic architecture of quantitative traits differs widely, with some traits exhibiting few if any quantitative trait loci (QTL) with large effects, while other traits have one or several easily detectable QTL with large effects. METHODS: Body weight in broilers and egg weight in layers are two examples of traits that have QTL of large effect. A commonly used method for genome wide association studies is to fit a mixture model such as BayesB that assumes some known proportion of SNP effects are zero. In contrast, the most commonly used method for genomic prediction is known as GBLUP, which involves fitting an animal model to phenotypic data with the variance-covariance or genomic relationship matrix among the animals being determined by genome wide SNP genotypes. Genotypes at each SNP are typically weighted equally in determining the genomic relationship matrix for GBLUP. We used the equivalent marker effects model formulation of GBLUP for this study. We compare these two classes of models using egg weight data collected over 8 generations from 2,324 animals genotyped with a 42 K SNP panel. RESULTS: Using data from the first 7 generations, both BayesB and GBLUP found the largest QTL in a similar well-recognized QTL region, but this QTL was estimated to account for 24 % of genetic variation with BayesB and less than 1 % with GBLUP. When predicting phenotypes in generation 8 BayesB accounted for 36 % of the phenotypic variation and GBLUP for 25 %. When using only data from any one generation, the same QTL was identified with BayesB in all but one generation but never with GBLUP. Predictions of phenotypes in generations 2 to 7 based on only 295 animals from generation 1 accounted for 10 % phenotypic variation with BayesB but only 6 % with GBLUP. Predicting phenotype using only the marker effects in the 1 Mb region that accounted for the largest effect on egg weight from generation 1 data alone accounted for almost 8 % variation using BayesB but had no predictive power with GBLUP. CONCLUSIONS: In conclusion, In the presence of large effect QTL, BayesB did a better job of QTL detection and its genomic predictions were more accurate and persistent than those from GBLUP. BioMed Central 2016-02-11 /pmc/articles/PMC4750167/ /pubmed/26870325 http://dx.doi.org/10.1186/s40104-016-0066-z Text en © Wolc et al. 2016 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Wolc, Anna Arango, Jesus Settar, Petek Fulton, Janet E. O’Sullivan, Neil P. Dekkers, Jack C. M. Fernando, Rohan Garrick, Dorian J. Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions |
title | Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions |
title_full | Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions |
title_fullStr | Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions |
title_full_unstemmed | Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions |
title_short | Mixture models detect large effect QTL better than GBLUP and result in more accurate and persistent predictions |
title_sort | mixture models detect large effect qtl better than gblup and result in more accurate and persistent predictions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4750167/ https://www.ncbi.nlm.nih.gov/pubmed/26870325 http://dx.doi.org/10.1186/s40104-016-0066-z |
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