Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approach

Abstract Background Samples of molecular sequence data of a locus obtained from random individuals in a population are often related by an unknown genealogy. More importantly, population genetics parameters, for instance, the scaled population mutation rate Θ=4N e μ for diploids or Θ=2N e μ for hapl...

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Main Authors: Oyetunji E. Ogundijo, Xiaodong Wang
Format: Article
Language:English
Published: BMC 2017-12-01
Series:BMC Bioinformatics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12859-017-1948-6
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spelling doaj-774f1888996a48ba87e795ab15d5ca252020-11-24T21:17:09ZengBMCBMC Bioinformatics1471-21052017-12-0118111510.1186/s12859-017-1948-6Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approachOyetunji E. Ogundijo0Xiaodong Wang1Department of Electrical Engineering, Columbia UniversityDepartment of Electrical Engineering, Columbia UniversityAbstract Background Samples of molecular sequence data of a locus obtained from random individuals in a population are often related by an unknown genealogy. More importantly, population genetics parameters, for instance, the scaled population mutation rate Θ=4N e μ for diploids or Θ=2N e μ for haploids (where N e is the effective population size and μ is the mutation rate per site per generation), which explains some of the evolutionary history and past qualities of the population that the samples are obtained from, is of significant interest. Results In this paper, we present the evolution of sequence data in a Bayesian framework and the approximation of the posterior distributions of the unknown parameters of the model, which include Θ via the sequential Monte Carlo (SMC) samplers for static models. Specifically, we approximate the posterior distributions of the unknown parameters with a set of weighted samples i.e., the set of highly probable genealogies out of the infinite set of possible genealogies that describe the sampled sequences. The proposed SMC algorithm is evaluated on simulated DNA sequence datasets under different mutational models and real biological sequences. In terms of the accuracy of the estimates, the proposed SMC method shows a comparable and sometimes, better performance than the state-of-the-art MCMC algorithms. Conclusions We showed that the SMC algorithm for static model is a promising alternative to the state-of-the-art approach for simulating from the posterior distributions of population genetics parameters.http://link.springer.com/article/10.1186/s12859-017-1948-6CoalescentSequential Monte CarloGenealogyBayesian
collection DOAJ
language English
format Article
sources DOAJ
author Oyetunji E. Ogundijo
Xiaodong Wang
spellingShingle Oyetunji E. Ogundijo
Xiaodong Wang
Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approach
BMC Bioinformatics
Coalescent
Sequential Monte Carlo
Genealogy
Bayesian
author_facet Oyetunji E. Ogundijo
Xiaodong Wang
author_sort Oyetunji E. Ogundijo
title Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approach
title_short Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approach
title_full Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approach
title_fullStr Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approach
title_full_unstemmed Bayesian estimation of scaled mutation rate under the coalescent: a sequential Monte Carlo approach
title_sort bayesian estimation of scaled mutation rate under the coalescent: a sequential monte carlo approach
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2017-12-01
description Abstract Background Samples of molecular sequence data of a locus obtained from random individuals in a population are often related by an unknown genealogy. More importantly, population genetics parameters, for instance, the scaled population mutation rate Θ=4N e μ for diploids or Θ=2N e μ for haploids (where N e is the effective population size and μ is the mutation rate per site per generation), which explains some of the evolutionary history and past qualities of the population that the samples are obtained from, is of significant interest. Results In this paper, we present the evolution of sequence data in a Bayesian framework and the approximation of the posterior distributions of the unknown parameters of the model, which include Θ via the sequential Monte Carlo (SMC) samplers for static models. Specifically, we approximate the posterior distributions of the unknown parameters with a set of weighted samples i.e., the set of highly probable genealogies out of the infinite set of possible genealogies that describe the sampled sequences. The proposed SMC algorithm is evaluated on simulated DNA sequence datasets under different mutational models and real biological sequences. In terms of the accuracy of the estimates, the proposed SMC method shows a comparable and sometimes, better performance than the state-of-the-art MCMC algorithms. Conclusions We showed that the SMC algorithm for static model is a promising alternative to the state-of-the-art approach for simulating from the posterior distributions of population genetics parameters.
topic Coalescent
Sequential Monte Carlo
Genealogy
Bayesian
url http://link.springer.com/article/10.1186/s12859-017-1948-6
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