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Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships

BACKGROUND: GBLUP (genomic best linear unbiased prediction) uses high-density single nucleotide polymorphism (SNP) markers to construct genomic identity-by-state (IBS) relationship matrices. However, identity-by-descent (IBD) relationships can be accurately calculated for extremely sparse markers. H...

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Autores principales: Vela-Avitúa, Sergio, Meuwissen, Theo HE, Luan, Tu, Ødegård, Jørgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339014/
https://www.ncbi.nlm.nih.gov/pubmed/25888184
http://dx.doi.org/10.1186/s12711-014-0084-2
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author Vela-Avitúa, Sergio
Meuwissen, Theo HE
Luan, Tu
Ødegård, Jørgen
author_facet Vela-Avitúa, Sergio
Meuwissen, Theo HE
Luan, Tu
Ødegård, Jørgen
author_sort Vela-Avitúa, Sergio
collection PubMed
description BACKGROUND: GBLUP (genomic best linear unbiased prediction) uses high-density single nucleotide polymorphism (SNP) markers to construct genomic identity-by-state (IBS) relationship matrices. However, identity-by-descent (IBD) relationships can be accurately calculated for extremely sparse markers. Here, we compare the accuracy of prediction of genome-wide breeding values (GW-BV) for a sib-evaluated trait in a typical aquaculture population, assuming either IBS or IBD genomic relationship matrices, and by varying marker density and size of the training dataset. METHODS: A simulation study was performed, assuming a population with strong family structure over three subsequent generations. Traditional and genomic BLUP were used to estimate breeding values, the latter using either IBS or IBD genomic relationship matrices, with marker densities ranging from 10 to ~1200 SNPs/Morgan (M). Heritability ranged from 0.1 to 0.8, and phenotypes were recorded on 25 to 45 sibs per full-sib family (50 full-sib families). Models were compared based on their predictive ability (accuracy) with respect to true breeding values of unphenotyped (albeit genotyped) sibs in the last generation. RESULTS: As expected, genomic prediction had greater accuracy compared to pedigree-based prediction. At the highest marker density, genomic prediction based on IBS information (IBS-GS) was slightly superior to that based on IBD information (IBD-GS), while at lower densities (≤100 SNPs/M), IBD-GS was more accurate. At the lowest densities (10 to 20 SNPs/M), IBS-GS was even outperformed by the pedigree-based model. Accuracy of IBD-GS was stable across marker densities performing well even down to 10 SNPs/M (2.5 to 6.1% reduction in accuracy compared to ~1200 SNPs/M). Loss of accuracy due to reduction in the size of training datasets was moderate and similar for both genomic prediction models. The relative superiority of (high-density) IBS-GS over IBD-GS was more pronounced for traits with a low heritability. CONCLUSIONS: Using dense markers, GBLUP based on either IBD or IBS relationship matrices proved to perform better than a pedigree-based model. However, accuracy of IBS-GS declined rapidly with decreasing marker densities, and was even outperformed by a traditional pedigree-based model at the lowest densities. In contrast, the accuracy of IBD-GS was very stable across marker densities.
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spelling pubmed-43390142015-02-25 Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships Vela-Avitúa, Sergio Meuwissen, Theo HE Luan, Tu Ødegård, Jørgen Genet Sel Evol Research BACKGROUND: GBLUP (genomic best linear unbiased prediction) uses high-density single nucleotide polymorphism (SNP) markers to construct genomic identity-by-state (IBS) relationship matrices. However, identity-by-descent (IBD) relationships can be accurately calculated for extremely sparse markers. Here, we compare the accuracy of prediction of genome-wide breeding values (GW-BV) for a sib-evaluated trait in a typical aquaculture population, assuming either IBS or IBD genomic relationship matrices, and by varying marker density and size of the training dataset. METHODS: A simulation study was performed, assuming a population with strong family structure over three subsequent generations. Traditional and genomic BLUP were used to estimate breeding values, the latter using either IBS or IBD genomic relationship matrices, with marker densities ranging from 10 to ~1200 SNPs/Morgan (M). Heritability ranged from 0.1 to 0.8, and phenotypes were recorded on 25 to 45 sibs per full-sib family (50 full-sib families). Models were compared based on their predictive ability (accuracy) with respect to true breeding values of unphenotyped (albeit genotyped) sibs in the last generation. RESULTS: As expected, genomic prediction had greater accuracy compared to pedigree-based prediction. At the highest marker density, genomic prediction based on IBS information (IBS-GS) was slightly superior to that based on IBD information (IBD-GS), while at lower densities (≤100 SNPs/M), IBD-GS was more accurate. At the lowest densities (10 to 20 SNPs/M), IBS-GS was even outperformed by the pedigree-based model. Accuracy of IBD-GS was stable across marker densities performing well even down to 10 SNPs/M (2.5 to 6.1% reduction in accuracy compared to ~1200 SNPs/M). Loss of accuracy due to reduction in the size of training datasets was moderate and similar for both genomic prediction models. The relative superiority of (high-density) IBS-GS over IBD-GS was more pronounced for traits with a low heritability. CONCLUSIONS: Using dense markers, GBLUP based on either IBD or IBS relationship matrices proved to perform better than a pedigree-based model. However, accuracy of IBS-GS declined rapidly with decreasing marker densities, and was even outperformed by a traditional pedigree-based model at the lowest densities. In contrast, the accuracy of IBD-GS was very stable across marker densities. BioMed Central 2015-02-25 /pmc/articles/PMC4339014/ /pubmed/25888184 http://dx.doi.org/10.1186/s12711-014-0084-2 Text en © Vela-Avitúa et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Vela-Avitúa, Sergio
Meuwissen, Theo HE
Luan, Tu
Ødegård, Jørgen
Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships
title Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships
title_full Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships
title_fullStr Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships
title_full_unstemmed Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships
title_short Accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships
title_sort accuracy of genomic selection for a sib-evaluated trait using identity-by-state and identity-by-descent relationships
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339014/
https://www.ncbi.nlm.nih.gov/pubmed/25888184
http://dx.doi.org/10.1186/s12711-014-0084-2
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