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Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon

Genomic selection has a great potential in aquaculture breeding since many important traits are not directly measured on the candidates themselves. However, its implementation has been hindered by staggering genotyping costs because of many individual genotypes. In this study, we explored the potent...

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Autores principales: Dagnachew, Binyam, Aslam, Muhammad Luqman, Hillestad, Borghild, Meuwissen, Theo, Sonesson, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459107/
https://www.ncbi.nlm.nih.gov/pubmed/36092907
http://dx.doi.org/10.3389/fgene.2022.896774
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author Dagnachew, Binyam
Aslam, Muhammad Luqman
Hillestad, Borghild
Meuwissen, Theo
Sonesson, Anna
author_facet Dagnachew, Binyam
Aslam, Muhammad Luqman
Hillestad, Borghild
Meuwissen, Theo
Sonesson, Anna
author_sort Dagnachew, Binyam
collection PubMed
description Genomic selection has a great potential in aquaculture breeding since many important traits are not directly measured on the candidates themselves. However, its implementation has been hindered by staggering genotyping costs because of many individual genotypes. In this study, we explored the potential of DNA pooling for creating a reference population as a tool for genomic selection of a binary trait. Two datasets from the SalmoBreed population challenged with salmonid alphavirus, which causes pancreas disease, were used. Dataset-1, that includes 855 individuals (478 survivors and 377 dead), was used to develop four DNA pool samples (i.e., 2 pools each for dead and survival). Dataset-2 includes 914 individuals (435 survivors and 479 dead) belonging to 65 full-sibling families and was used to develop in-silico DNA pools. SNP effects from the pool data were calculated based on allele frequencies estimated from the pools and used to calculate genomic breeding values (GEBVs). The correlation between SNP effects estimated based on individual genotypes and pooled data increased from 0.3 to 0.912 when the number of pools increased from 1 to 200. A similar trend was also observed for the correlation between GEBVs, which increased from 0.84 to 0.976, as the number of pools per phenotype increased from 1 to 200. For dataset-1, the accuracy of prediction was 0.71 and 0.70 when the DNA pools were sequenced in 40× and 20×, respectively, compared to an accuracy of 0.73 for the SNP chip genotypes. For dataset-2, the accuracy of prediction increased from 0.574 to 0.691 when the number of in-silico DNA pools increased from 1 to 200. For this dataset, the accuracy of prediction using individual genotypes was 0.712. A limited effect of sequencing depth on the correlation of GEBVs and prediction accuracy was observed. Results showed that a large number of pools are required to achieve as good prediction as individual genotypes; however, alternative effective pooling strategies should be studied to reduce the number of pools without reducing the prediction power. Nevertheless, it is demonstrated that pooling of a reference population can be used as a tool to optimize between cost and accuracy of selection.
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spelling pubmed-94591072022-09-10 Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon Dagnachew, Binyam Aslam, Muhammad Luqman Hillestad, Borghild Meuwissen, Theo Sonesson, Anna Front Genet Genetics Genomic selection has a great potential in aquaculture breeding since many important traits are not directly measured on the candidates themselves. However, its implementation has been hindered by staggering genotyping costs because of many individual genotypes. In this study, we explored the potential of DNA pooling for creating a reference population as a tool for genomic selection of a binary trait. Two datasets from the SalmoBreed population challenged with salmonid alphavirus, which causes pancreas disease, were used. Dataset-1, that includes 855 individuals (478 survivors and 377 dead), was used to develop four DNA pool samples (i.e., 2 pools each for dead and survival). Dataset-2 includes 914 individuals (435 survivors and 479 dead) belonging to 65 full-sibling families and was used to develop in-silico DNA pools. SNP effects from the pool data were calculated based on allele frequencies estimated from the pools and used to calculate genomic breeding values (GEBVs). The correlation between SNP effects estimated based on individual genotypes and pooled data increased from 0.3 to 0.912 when the number of pools increased from 1 to 200. A similar trend was also observed for the correlation between GEBVs, which increased from 0.84 to 0.976, as the number of pools per phenotype increased from 1 to 200. For dataset-1, the accuracy of prediction was 0.71 and 0.70 when the DNA pools were sequenced in 40× and 20×, respectively, compared to an accuracy of 0.73 for the SNP chip genotypes. For dataset-2, the accuracy of prediction increased from 0.574 to 0.691 when the number of in-silico DNA pools increased from 1 to 200. For this dataset, the accuracy of prediction using individual genotypes was 0.712. A limited effect of sequencing depth on the correlation of GEBVs and prediction accuracy was observed. Results showed that a large number of pools are required to achieve as good prediction as individual genotypes; however, alternative effective pooling strategies should be studied to reduce the number of pools without reducing the prediction power. Nevertheless, it is demonstrated that pooling of a reference population can be used as a tool to optimize between cost and accuracy of selection. Frontiers Media S.A. 2022-08-26 /pmc/articles/PMC9459107/ /pubmed/36092907 http://dx.doi.org/10.3389/fgene.2022.896774 Text en Copyright © 2022 Dagnachew, Aslam, Hillestad, Meuwissen and Sonesson. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Dagnachew, Binyam
Aslam, Muhammad Luqman
Hillestad, Borghild
Meuwissen, Theo
Sonesson, Anna
Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon
title Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon
title_full Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon
title_fullStr Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon
title_full_unstemmed Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon
title_short Use of DNA pools of a reference population for genomic selection of a binary trait in Atlantic salmon
title_sort use of dna pools of a reference population for genomic selection of a binary trait in atlantic salmon
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9459107/
https://www.ncbi.nlm.nih.gov/pubmed/36092907
http://dx.doi.org/10.3389/fgene.2022.896774
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