Email updates

Keep up to date with the latest news and content from BMC Bioinformatics and BioMed Central.

Open Access Highly Accessed Methodology article

Bayesian coestimation of phylogeny and sequence alignment

Gerton Lunter1*, István Miklós2, Alexei Drummond3, Jens Ledet Jensen4 and Jotun Hein1

Author affiliations

1 Department of Statistics, University of Oxford, 1 South Parks Road, Oxford OX1 3TG, UK

2 MTA-ELTE Theoretical Biology and Ecology Group, Pázmány Péter sétány 1/c 1117 Budapest, Hungary

3 Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK

4 Department of Mathematical Sciences, University of Aarhus, Ny Munkegade, Building 530, DK-8000 Aarhus C, Denmark

For all author emails, please log on.

Citation and License

BMC Bioinformatics 2005, 6:83  doi:10.1186/1471-2105-6-83

Published: 1 April 2005

Abstract

Background

Two central problems in computational biology are the determination of the alignment and phylogeny of a set of biological sequences. The traditional approach to this problem is to first build a multiple alignment of these sequences, followed by a phylogenetic reconstruction step based on this multiple alignment. However, alignment and phylogenetic inference are fundamentally interdependent, and ignoring this fact leads to biased and overconfident estimations. Whether the main interest be in sequence alignment or phylogeny, a major goal of computational biology is the co-estimation of both.

Results

We developed a fully Bayesian Markov chain Monte Carlo method for coestimating phylogeny and sequence alignment, under the Thorne-Kishino-Felsenstein model of substitution and single nucleotide insertion-deletion (indel) events. In our earlier work, we introduced a novel and efficient algorithm, termed the "indel peeling algorithm", which includes indels as phylogenetically informative evolutionary events, and resembles Felsenstein's peeling algorithm for substitutions on a phylogenetic tree. For a fixed alignment, our extension analytically integrates out both substitution and indel events within a proper statistical model, without the need for data augmentation at internal tree nodes, allowing for efficient sampling of tree topologies and edge lengths. To additionally sample multiple alignments, we here introduce an efficient partial Metropolized independence sampler for alignments, and combine these two algorithms into a fully Bayesian co-estimation procedure for the alignment and phylogeny problem.

Our approach results in estimates for the posterior distribution of evolutionary rate parameters, for the maximum a-posteriori (MAP) phylogenetic tree, and for the posterior decoding alignment. Estimates for the evolutionary tree and multiple alignment are augmented with confidence estimates for each node height and alignment column. Our results indicate that the patterns in reliability broadly correspond to structural features of the proteins, and thus provides biologically meaningful information which is not existent in the usual point-estimate of the alignment. Our methods can handle input data of moderate size (10–20 protein sequences, each 100–200 bp), which we analyzed overnight on a standard 2 GHz personal computer.

Conclusion

Joint analysis of multiple sequence alignment, evolutionary trees and additional evolutionary parameters can be now done within a single coherent statistical framework.