Home LiteratureArticle Details
PMID: 17095535 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Bayesian estimation of concordance among gene trees.

Molecular biology and evolution ·Vol. 24 ·No. 2 ·2007-02-00 ·Pages 412-26

Ané C, Larget B, Baum DA, Smith SD, Rokas A

Abstract

Multigene sequence data have great potential for elucidating important and interesting evolutionary processes, but statistical methods for extracting information from such data remain limited. Although various biological processes may cause different genes to have different genealogical histories (and hence different tree topologies), we also may expect that the number of distinct topologies among a set of genes is relatively small compared with the number of possible topologies. Therefore evidence about the tree topology for one gene should influence our inferences of the tree topology on a different gene, but to what extent? In this paper, we present a new approach for modeling and estimating concordance among a set of gene trees given aligned molecular sequence data. Our approach introduces a one-parameter probability distribution to describe the prior distribution of concordance among gene trees. We describe a novel 2-stage Markov chain Monte Carlo (MCMC) method that first obtains independent Bayesian posterior probability distributions for individual genes using standard methods. These posterior distributions are then used as input for a second MCMC procedure that estimates a posterior distribution of gene-to-tree maps (GTMs). The posterior distribution of GTMs can then be summarized to provide revised posterior probability distributions for each gene (taking account of concordance) and to allow estimation of the proportion of the sampled genes for which any given clade is true (the sample-wide concordance factor). Further, under the assumption that the sampled genes are drawn randomly from a genome of known size, we show how one can obtain an estimate, with credibility intervals, on the proportion of the entire genome for which a clade is true (the genome-wide concordance factor). We demonstrate the method on a set of 106 genes from 8 yeast species.

MeSH Terms
Algorithms Base Sequence Bayes Theorem Evolution, Molecular Genes Markov Chains Models, Genetic Monte Carlo Method Phylogeny Saccharomyces/genetics Sequence Alignment
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ané Cécile
Department of Statistics, University of Wisconsin, USA. [email protected]
Larget Bret
Baum David A
Smith Stacey D
Rokas Antonis
Article Info
Journal
Molecular biology and evolution
Abbr.
Mol Biol Evol
ISSN
0737-4038
Published
2007-02-00
Epub
2006-00-09
Pages
412-26
Language
English
Region
United States
NLM ID
8501455
Subset
IM
Grants
NIGMS NIH HHS · R01 GM068950 · United States
NIGMS NIH HHS · R01 GM069801 · United States
Corrections
ErratumIn
-
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]