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Genomic prediction from observed and imputed high-density ovine genotypes

BACKGROUND: Genomic prediction using high-density (HD) marker genotypes is expected to lead to higher prediction accuracy, particularly for more heterogeneous multi-breed and crossbred populations such as those in sheep and beef cattle, due to providing stronger linkage disequilibrium between single...

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Autores principales: Moghaddar, Nasir, Swan, Andrew A., van der Werf, Julius H. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399335/
https://www.ncbi.nlm.nih.gov/pubmed/28427324
http://dx.doi.org/10.1186/s12711-017-0315-4
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author Moghaddar, Nasir
Swan, Andrew A.
van der Werf, Julius H. J.
author_facet Moghaddar, Nasir
Swan, Andrew A.
van der Werf, Julius H. J.
author_sort Moghaddar, Nasir
collection PubMed
description BACKGROUND: Genomic prediction using high-density (HD) marker genotypes is expected to lead to higher prediction accuracy, particularly for more heterogeneous multi-breed and crossbred populations such as those in sheep and beef cattle, due to providing stronger linkage disequilibrium between single nucleotide polymorphisms and quantitative trait loci controlling a trait. The objective of this study was to evaluate a possible improvement in genomic prediction accuracy of production traits in Australian sheep breeds based on HD genotypes (600k, both observed and imputed) compared to prediction based on 50k marker genotypes. In particular, we compared improvement in prediction accuracy of animals that are more distantly related to the reference population and across sheep breeds. METHODS: Genomic best linear unbiased prediction (GBLUP) and a Bayesian approach (BayesR) were used as prediction methods using whole or subsets of a large multi-breed/crossbred sheep reference set. Empirical prediction accuracy was evaluated for purebred Merino, Border Leicester, Poll Dorset and White Suffolk sire breeds according to the Pearson correlation coefficient between genomic estimated breeding values and breeding values estimated based on a progeny test in a separate dataset. RESULTS: Results showed a small absolute improvement (0.0 to 8.0% and on average 2.2% across all traits) in prediction accuracy of purebred animals from HD genotypes when prediction was based on the whole dataset. Greater improvement in prediction accuracy (1.0 to 12.0% and on average 5.2%) was observed for animals that were genetically lowly related to the reference set while it ranged from 0.0 to 5.0% for across-breed prediction. On average, no significant advantage was observed with BayesR compared to GBLUP.
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spelling pubmed-53993352017-04-24 Genomic prediction from observed and imputed high-density ovine genotypes Moghaddar, Nasir Swan, Andrew A. van der Werf, Julius H. J. Genet Sel Evol Short Communication BACKGROUND: Genomic prediction using high-density (HD) marker genotypes is expected to lead to higher prediction accuracy, particularly for more heterogeneous multi-breed and crossbred populations such as those in sheep and beef cattle, due to providing stronger linkage disequilibrium between single nucleotide polymorphisms and quantitative trait loci controlling a trait. The objective of this study was to evaluate a possible improvement in genomic prediction accuracy of production traits in Australian sheep breeds based on HD genotypes (600k, both observed and imputed) compared to prediction based on 50k marker genotypes. In particular, we compared improvement in prediction accuracy of animals that are more distantly related to the reference population and across sheep breeds. METHODS: Genomic best linear unbiased prediction (GBLUP) and a Bayesian approach (BayesR) were used as prediction methods using whole or subsets of a large multi-breed/crossbred sheep reference set. Empirical prediction accuracy was evaluated for purebred Merino, Border Leicester, Poll Dorset and White Suffolk sire breeds according to the Pearson correlation coefficient between genomic estimated breeding values and breeding values estimated based on a progeny test in a separate dataset. RESULTS: Results showed a small absolute improvement (0.0 to 8.0% and on average 2.2% across all traits) in prediction accuracy of purebred animals from HD genotypes when prediction was based on the whole dataset. Greater improvement in prediction accuracy (1.0 to 12.0% and on average 5.2%) was observed for animals that were genetically lowly related to the reference set while it ranged from 0.0 to 5.0% for across-breed prediction. On average, no significant advantage was observed with BayesR compared to GBLUP. BioMed Central 2017-04-20 /pmc/articles/PMC5399335/ /pubmed/28427324 http://dx.doi.org/10.1186/s12711-017-0315-4 Text en © The Author(s) 2017 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 Short Communication
Moghaddar, Nasir
Swan, Andrew A.
van der Werf, Julius H. J.
Genomic prediction from observed and imputed high-density ovine genotypes
title Genomic prediction from observed and imputed high-density ovine genotypes
title_full Genomic prediction from observed and imputed high-density ovine genotypes
title_fullStr Genomic prediction from observed and imputed high-density ovine genotypes
title_full_unstemmed Genomic prediction from observed and imputed high-density ovine genotypes
title_short Genomic prediction from observed and imputed high-density ovine genotypes
title_sort genomic prediction from observed and imputed high-density ovine genotypes
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399335/
https://www.ncbi.nlm.nih.gov/pubmed/28427324
http://dx.doi.org/10.1186/s12711-017-0315-4
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