4.8 Article

Bayesian phylogenetic model selection using reversible jump Markov chain Monte Carlo

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 21, Issue 6, Pages 1123-1133

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msh123

Keywords

Bayesian phylogenetic inference; Markov chain Monte Carlo; maximum likelihood; reversible jump Markov chain Monte Carlo; substitution models

Funding

  1. NIGMS NIH HHS [R01 GM68950-01, R01 GM069801] Funding Source: Medline

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A common problem in molecular phylogenetics is choosing a model of DNA substitution that does a good job of explaining the DNA sequence alignment without introducing superfluous parameters. A number of methods have been used to choose among a small set of candidate substitution models, such as the likelihood ratio test, the Akaike Information Criterion (AIC), tire Bayesian Information Criterion (BIC), and Bayes factors. Current implementations of any of these criteria suffer from the limitation that only a small set of models are examined, or that the test does not allow easy comparison of non-nested models. In this article, we expand the pool of candidate substitution models to include all possible time-reversible models. This set includes seven models that have already been described. We show how Bayes factors can be calculated for these models using reversible jump Markov chain Monte Carlo, and apply the method to 16 DNA sequence alignments. For each data set, we compare the model with the best Bayes factor to the best models chosen using AIC and BIC. We find that the best model under any of these criteria is not necessarily the most complicated one; models with an intermediate number of substitution types typically do best. Moreover, almost all of the models that are chosen as best do not constrain a transition rate to be the same as a transversion rate, suggesting that it is the transition/transversion rate bias that plays the largest role in determining which models are selected. Importantly, the reversible jump Markov chain Monte Carlo algorithm described here allows estimation of phylogeny (and other phylogenetic model parameters) to be performed while accounting for uncertainty in the model of DNA substitution.

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