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Using a very low-density SNP panel for genomic selection in a breeding program for sheep

BACKGROUND: Building an efficient reference population for genomic selection is an issue when the recorded population is small and phenotypes are poorly informed, which is often the case in sheep breeding programs. Using stochastic simulation, we evaluated a genomic design based on a reference popul...

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Autores principales: Raoul, Jérôme, Swan, Andrew A., Elsen, Jean-Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655911/
https://www.ncbi.nlm.nih.gov/pubmed/29065868
http://dx.doi.org/10.1186/s12711-017-0351-0
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author Raoul, Jérôme
Swan, Andrew A.
Elsen, Jean-Michel
author_facet Raoul, Jérôme
Swan, Andrew A.
Elsen, Jean-Michel
author_sort Raoul, Jérôme
collection PubMed
description BACKGROUND: Building an efficient reference population for genomic selection is an issue when the recorded population is small and phenotypes are poorly informed, which is often the case in sheep breeding programs. Using stochastic simulation, we evaluated a genomic design based on a reference population with medium-density genotypes [around 45 K single nucleotide polymorphisms (SNPs)] of dams that were imputed from very low-density genotypes (≤ 1000 SNPs). METHODS: A population under selection for a maternal trait was simulated using real genotypes. Genetic gains realized from classical selection and genomic selection designs were compared. Genomic selection scenarios that differed in reference population structure (whether or not dams were included in the reference) and genotype quality (medium-density or imputed to medium-density from very low-density) were evaluated. RESULTS: The genomic design increased genetic gain by 26% when the reference population was based on sire medium-density genotypes and by 54% when the reference population included both sire and dam medium-density genotypes. When medium-density genotypes of male candidates and dams were replaced by imputed genotypes from very low-density SNP genotypes (1000 SNPs), the increase in gain was 22% for the sire reference population and 42% for the sire and dam reference population. The rate of increase in inbreeding was lower (from − 20 to − 34%) for the genomic design than for the classical design regardless of the genomic scenario. CONCLUSIONS: We show that very low-density genotypes of male candidates and dams combined with an imputation process result in a substantial increase in genetic gain for small sheep breeding programs.
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spelling pubmed-56559112017-10-31 Using a very low-density SNP panel for genomic selection in a breeding program for sheep Raoul, Jérôme Swan, Andrew A. Elsen, Jean-Michel Genet Sel Evol Research Article BACKGROUND: Building an efficient reference population for genomic selection is an issue when the recorded population is small and phenotypes are poorly informed, which is often the case in sheep breeding programs. Using stochastic simulation, we evaluated a genomic design based on a reference population with medium-density genotypes [around 45 K single nucleotide polymorphisms (SNPs)] of dams that were imputed from very low-density genotypes (≤ 1000 SNPs). METHODS: A population under selection for a maternal trait was simulated using real genotypes. Genetic gains realized from classical selection and genomic selection designs were compared. Genomic selection scenarios that differed in reference population structure (whether or not dams were included in the reference) and genotype quality (medium-density or imputed to medium-density from very low-density) were evaluated. RESULTS: The genomic design increased genetic gain by 26% when the reference population was based on sire medium-density genotypes and by 54% when the reference population included both sire and dam medium-density genotypes. When medium-density genotypes of male candidates and dams were replaced by imputed genotypes from very low-density SNP genotypes (1000 SNPs), the increase in gain was 22% for the sire reference population and 42% for the sire and dam reference population. The rate of increase in inbreeding was lower (from − 20 to − 34%) for the genomic design than for the classical design regardless of the genomic scenario. CONCLUSIONS: We show that very low-density genotypes of male candidates and dams combined with an imputation process result in a substantial increase in genetic gain for small sheep breeding programs. BioMed Central 2017-10-24 /pmc/articles/PMC5655911/ /pubmed/29065868 http://dx.doi.org/10.1186/s12711-017-0351-0 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 Research Article
Raoul, Jérôme
Swan, Andrew A.
Elsen, Jean-Michel
Using a very low-density SNP panel for genomic selection in a breeding program for sheep
title Using a very low-density SNP panel for genomic selection in a breeding program for sheep
title_full Using a very low-density SNP panel for genomic selection in a breeding program for sheep
title_fullStr Using a very low-density SNP panel for genomic selection in a breeding program for sheep
title_full_unstemmed Using a very low-density SNP panel for genomic selection in a breeding program for sheep
title_short Using a very low-density SNP panel for genomic selection in a breeding program for sheep
title_sort using a very low-density snp panel for genomic selection in a breeding program for sheep
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655911/
https://www.ncbi.nlm.nih.gov/pubmed/29065868
http://dx.doi.org/10.1186/s12711-017-0351-0
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