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Fast parallelized sampling of Bayesian regression models for whole-genome prediction
BACKGROUND: Bayesian regression models are widely used in genomic prediction, where the effects of all markers are estimated simultaneously by combining the information from the phenotypic data with priors for the marker effects and other parameters such as variance components or membership probabil...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087391/ https://www.ncbi.nlm.nih.gov/pubmed/32293243 http://dx.doi.org/10.1186/s12711-020-00533-x |
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author | Zhao, Tianjing Fernando, Rohan Garrick, Dorian Cheng, Hao |
author_facet | Zhao, Tianjing Fernando, Rohan Garrick, Dorian Cheng, Hao |
author_sort | Zhao, Tianjing |
collection | PubMed |
description | BACKGROUND: Bayesian regression models are widely used in genomic prediction, where the effects of all markers are estimated simultaneously by combining the information from the phenotypic data with priors for the marker effects and other parameters such as variance components or membership probabilities. Inferences from most Bayesian regression models are based on Markov chain Monte Carlo methods, where statistics are computed from a Markov chain constructed to have a stationary distribution that is equal to the posterior distribution of the unknown parameters. In practice, chains of tens of thousands steps are typically used in whole-genome Bayesian analyses, which is computationally intensive. METHODS: In this paper, we propose a fast parallelized algorithm for Bayesian regression models called independent intensive Bayesian regression models (BayesXII, “X” stands for Bayesian alphabet methods and “II” stands for “parallel”) and show how the sampling of each marker effect can be made independent of samples for other marker effects within each step of the chain. This is done by augmenting the marker covariate matrix by adding p (the number of markers) new rows such that columns of the augmented marker covariate matrix are orthogonal. Ideally, the computations at each step of the MCMC chain can be accelerated by k times, where k is the number of computer processors, up to p times, where p is the number of markers. RESULTS: We demonstrate the BayesXII algorithm using the prior for BayesC[Formula: see text] , a Bayesian variable selection regression method, which is applied to simulated data with 50,000 individuals and a medium-density marker panel ([Formula: see text] 50,000 markers). To reach about the same accuracy as the conventional samplers for BayesC[Formula: see text] required less than 30 min using the BayesXII algorithm on 24 nodes (computer used as a server) with 24 cores on each node. In this case, the BayesXII algorithm required one tenth of the computation time of conventional samplers for BayesC[Formula: see text] . Addressing the heavy computational burden associated with Bayesian methods by parallel computing will lead to greater use of these methods. |
format | Online Article Text |
id | pubmed-7087391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70873912020-03-24 Fast parallelized sampling of Bayesian regression models for whole-genome prediction Zhao, Tianjing Fernando, Rohan Garrick, Dorian Cheng, Hao Genet Sel Evol Research Article BACKGROUND: Bayesian regression models are widely used in genomic prediction, where the effects of all markers are estimated simultaneously by combining the information from the phenotypic data with priors for the marker effects and other parameters such as variance components or membership probabilities. Inferences from most Bayesian regression models are based on Markov chain Monte Carlo methods, where statistics are computed from a Markov chain constructed to have a stationary distribution that is equal to the posterior distribution of the unknown parameters. In practice, chains of tens of thousands steps are typically used in whole-genome Bayesian analyses, which is computationally intensive. METHODS: In this paper, we propose a fast parallelized algorithm for Bayesian regression models called independent intensive Bayesian regression models (BayesXII, “X” stands for Bayesian alphabet methods and “II” stands for “parallel”) and show how the sampling of each marker effect can be made independent of samples for other marker effects within each step of the chain. This is done by augmenting the marker covariate matrix by adding p (the number of markers) new rows such that columns of the augmented marker covariate matrix are orthogonal. Ideally, the computations at each step of the MCMC chain can be accelerated by k times, where k is the number of computer processors, up to p times, where p is the number of markers. RESULTS: We demonstrate the BayesXII algorithm using the prior for BayesC[Formula: see text] , a Bayesian variable selection regression method, which is applied to simulated data with 50,000 individuals and a medium-density marker panel ([Formula: see text] 50,000 markers). To reach about the same accuracy as the conventional samplers for BayesC[Formula: see text] required less than 30 min using the BayesXII algorithm on 24 nodes (computer used as a server) with 24 cores on each node. In this case, the BayesXII algorithm required one tenth of the computation time of conventional samplers for BayesC[Formula: see text] . Addressing the heavy computational burden associated with Bayesian methods by parallel computing will lead to greater use of these methods. BioMed Central 2020-03-23 /pmc/articles/PMC7087391/ /pubmed/32293243 http://dx.doi.org/10.1186/s12711-020-00533-x Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Zhao, Tianjing Fernando, Rohan Garrick, Dorian Cheng, Hao Fast parallelized sampling of Bayesian regression models for whole-genome prediction |
title | Fast parallelized sampling of Bayesian regression models for whole-genome prediction |
title_full | Fast parallelized sampling of Bayesian regression models for whole-genome prediction |
title_fullStr | Fast parallelized sampling of Bayesian regression models for whole-genome prediction |
title_full_unstemmed | Fast parallelized sampling of Bayesian regression models for whole-genome prediction |
title_short | Fast parallelized sampling of Bayesian regression models for whole-genome prediction |
title_sort | fast parallelized sampling of bayesian regression models for whole-genome prediction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087391/ https://www.ncbi.nlm.nih.gov/pubmed/32293243 http://dx.doi.org/10.1186/s12711-020-00533-x |
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