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Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey

Low-coverage whole genome sequencing is a low-cost genotyping technology. Combined with genotype imputation approaches, it is likely to become a critical component of cost-effective genomic selection programs in agricultural livestock. Here, we used the low-coverage sequence data of 617 Dezhou donke...

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Autores principales: Zhao, Changheng, Teng, Jun, Zhang, Xinhao, Wang, Dan, Zhang, Xinyi, Li, Shiyin, Jiang, Xin, Li, Haijing, Ning, Chao, Zhang, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595392/
https://www.ncbi.nlm.nih.gov/pubmed/34804115
http://dx.doi.org/10.3389/fgene.2021.728764
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author Zhao, Changheng
Teng, Jun
Zhang, Xinhao
Wang, Dan
Zhang, Xinyi
Li, Shiyin
Jiang, Xin
Li, Haijing
Ning, Chao
Zhang, Qin
author_facet Zhao, Changheng
Teng, Jun
Zhang, Xinhao
Wang, Dan
Zhang, Xinyi
Li, Shiyin
Jiang, Xin
Li, Haijing
Ning, Chao
Zhang, Qin
author_sort Zhao, Changheng
collection PubMed
description Low-coverage whole genome sequencing is a low-cost genotyping technology. Combined with genotype imputation approaches, it is likely to become a critical component of cost-effective genomic selection programs in agricultural livestock. Here, we used the low-coverage sequence data of 617 Dezhou donkeys to investigate the performance of genotype imputation for low-coverage whole genome sequence data and genomic prediction based on the imputed genotype data. The specific aims were as follows: 1) to measure the accuracy of genotype imputation under different sequencing depths, sample sizes, minor allele frequency (MAF), and imputation pipelines and 2) to assess the accuracy of genomic prediction under different marker densities derived from the imputed sequence data, different strategies for constructing the genomic relationship matrixes, and single-vs. multi-trait models. We found that a high imputation accuracy (>0.95) can be achieved for sequence data with a sequencing depth as low as 1x and the number of sequenced individuals ≥400. For genomic prediction, the best performance was obtained by using a marker density of 410K and a G matrix constructed using expected marker dosages. Multi-trait genomic best linear unbiased prediction (GBLUP) performed better than single-trait GBLUP. Our study demonstrates that low-coverage whole genome sequencing would be a cost-effective approach for genomic prediction in Dezhou donkey.
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spelling pubmed-85953922021-11-18 Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey Zhao, Changheng Teng, Jun Zhang, Xinhao Wang, Dan Zhang, Xinyi Li, Shiyin Jiang, Xin Li, Haijing Ning, Chao Zhang, Qin Front Genet Genetics Low-coverage whole genome sequencing is a low-cost genotyping technology. Combined with genotype imputation approaches, it is likely to become a critical component of cost-effective genomic selection programs in agricultural livestock. Here, we used the low-coverage sequence data of 617 Dezhou donkeys to investigate the performance of genotype imputation for low-coverage whole genome sequence data and genomic prediction based on the imputed genotype data. The specific aims were as follows: 1) to measure the accuracy of genotype imputation under different sequencing depths, sample sizes, minor allele frequency (MAF), and imputation pipelines and 2) to assess the accuracy of genomic prediction under different marker densities derived from the imputed sequence data, different strategies for constructing the genomic relationship matrixes, and single-vs. multi-trait models. We found that a high imputation accuracy (>0.95) can be achieved for sequence data with a sequencing depth as low as 1x and the number of sequenced individuals ≥400. For genomic prediction, the best performance was obtained by using a marker density of 410K and a G matrix constructed using expected marker dosages. Multi-trait genomic best linear unbiased prediction (GBLUP) performed better than single-trait GBLUP. Our study demonstrates that low-coverage whole genome sequencing would be a cost-effective approach for genomic prediction in Dezhou donkey. Frontiers Media S.A. 2021-11-03 /pmc/articles/PMC8595392/ /pubmed/34804115 http://dx.doi.org/10.3389/fgene.2021.728764 Text en Copyright © 2021 Zhao, Teng, Zhang, Wang, Zhang, Li, Jiang, Li, Ning and Zhang. 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
Zhao, Changheng
Teng, Jun
Zhang, Xinhao
Wang, Dan
Zhang, Xinyi
Li, Shiyin
Jiang, Xin
Li, Haijing
Ning, Chao
Zhang, Qin
Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey
title Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey
title_full Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey
title_fullStr Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey
title_full_unstemmed Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey
title_short Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey
title_sort towards a cost-effective implementation of genomic prediction based on low coverage whole genome sequencing in dezhou donkey
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8595392/
https://www.ncbi.nlm.nih.gov/pubmed/34804115
http://dx.doi.org/10.3389/fgene.2021.728764
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