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BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis
Bayesian methods, such as BayesR, for predicting the genetic value or risk of individuals from their genotypes, such as Single Nucleotide Polymorphisms (SNP), are often implemented using a Markov Chain Monte Carlo (MCMC) process. However, the generation of Markov chains is computationally slow. We i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256732/ https://www.ncbi.nlm.nih.gov/pubmed/35790806 http://dx.doi.org/10.1038/s42003-022-03624-1 |
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author | Breen, Edmond J. MacLeod, Iona M. Ho, Phuong N. Haile-Mariam, Mekonnen Pryce, Jennie E. Thomas, Carl D. Daetwyler, Hans D. Goddard, Michael E. |
author_facet | Breen, Edmond J. MacLeod, Iona M. Ho, Phuong N. Haile-Mariam, Mekonnen Pryce, Jennie E. Thomas, Carl D. Daetwyler, Hans D. Goddard, Michael E. |
author_sort | Breen, Edmond J. |
collection | PubMed |
description | Bayesian methods, such as BayesR, for predicting the genetic value or risk of individuals from their genotypes, such as Single Nucleotide Polymorphisms (SNP), are often implemented using a Markov Chain Monte Carlo (MCMC) process. However, the generation of Markov chains is computationally slow. We introduce a form of blocked Gibbs sampling for estimating SNP effects from Markov chains that greatly reduces computational time by sampling each SNP effect iteratively n-times from conditional block posteriors. Subsequent iteration over all blocks m-times produces chains of length m × n. We use this strategy to solve large-scale genomic prediction and fine-mapping problems using the Bayesian MCMC mixed-effects genetic model, BayesR3. We validate the method using simulated data, followed by analysis of empirical dairy cattle data using high dimension milk mid infra-red spectra data as an example of “omics” data and show its use to increase the precision of mapping variants affecting milk, fat, and protein yields relative to a univariate analysis of milk, fat, and protein. |
format | Online Article Text |
id | pubmed-9256732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-92567322022-07-07 BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis Breen, Edmond J. MacLeod, Iona M. Ho, Phuong N. Haile-Mariam, Mekonnen Pryce, Jennie E. Thomas, Carl D. Daetwyler, Hans D. Goddard, Michael E. Commun Biol Article Bayesian methods, such as BayesR, for predicting the genetic value or risk of individuals from their genotypes, such as Single Nucleotide Polymorphisms (SNP), are often implemented using a Markov Chain Monte Carlo (MCMC) process. However, the generation of Markov chains is computationally slow. We introduce a form of blocked Gibbs sampling for estimating SNP effects from Markov chains that greatly reduces computational time by sampling each SNP effect iteratively n-times from conditional block posteriors. Subsequent iteration over all blocks m-times produces chains of length m × n. We use this strategy to solve large-scale genomic prediction and fine-mapping problems using the Bayesian MCMC mixed-effects genetic model, BayesR3. We validate the method using simulated data, followed by analysis of empirical dairy cattle data using high dimension milk mid infra-red spectra data as an example of “omics” data and show its use to increase the precision of mapping variants affecting milk, fat, and protein yields relative to a univariate analysis of milk, fat, and protein. Nature Publishing Group UK 2022-07-05 /pmc/articles/PMC9256732/ /pubmed/35790806 http://dx.doi.org/10.1038/s42003-022-03624-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Breen, Edmond J. MacLeod, Iona M. Ho, Phuong N. Haile-Mariam, Mekonnen Pryce, Jennie E. Thomas, Carl D. Daetwyler, Hans D. Goddard, Michael E. BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis |
title | BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis |
title_full | BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis |
title_fullStr | BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis |
title_full_unstemmed | BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis |
title_short | BayesR3 enables fast MCMC blocked processing for largescale multi-trait genomic prediction and QTN mapping analysis |
title_sort | bayesr3 enables fast mcmc blocked processing for largescale multi-trait genomic prediction and qtn mapping analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9256732/ https://www.ncbi.nlm.nih.gov/pubmed/35790806 http://dx.doi.org/10.1038/s42003-022-03624-1 |
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