Literature DB >> 22403239

Improving the accuracy of demographic and molecular clock model comparison while accommodating phylogenetic uncertainty.

Guy Baele1, Philippe Lemey, Trevor Bedford, Andrew Rambaut, Marc A Suchard, Alexander V Alekseyenko.   

Abstract

Recent developments in marginal likelihood estimation for model selection in the field of Bayesian phylogenetics and molecular evolution have emphasized the poor performance of the harmonic mean estimator (HME). Although these studies have shown the merits of new approaches applied to standard normally distributed examples and small real-world data sets, not much is currently known concerning the performance and computational issues of these methods when fitting complex evolutionary and population genetic models to empirical real-world data sets. Further, these approaches have not yet seen widespread application in the field due to the lack of implementations of these computationally demanding techniques in commonly used phylogenetic packages. We here investigate the performance of some of these new marginal likelihood estimators, specifically, path sampling (PS) and stepping-stone (SS) sampling for comparing models of demographic change and relaxed molecular clocks, using synthetic data and real-world examples for which unexpected inferences were made using the HME. Given the drastically increased computational demands of PS and SS sampling, we also investigate a posterior simulation-based analogue of Akaike's information criterion (AIC) through Markov chain Monte Carlo (MCMC), a model comparison approach that shares with the HME the appealing feature of having a low computational overhead over the original MCMC analysis. We confirm that the HME systematically overestimates the marginal likelihood and fails to yield reliable model classification and show that the AICM performs better and may be a useful initial evaluation of model choice but that it is also, to a lesser degree, unreliable. We show that PS and SS sampling substantially outperform these estimators and adjust the conclusions made concerning previous analyses for the three real-world data sets that we reanalyzed. The methods used in this article are now available in BEAST, a powerful user-friendly software package to perform Bayesian evolutionary analyses.

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Year:  2012        PMID: 22403239      PMCID: PMC3424409          DOI: 10.1093/molbev/mss084

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  27 in total

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4.  A general comparison of relaxed molecular clock models.

Authors:  Thomas Lepage; David Bryant; Hervé Philippe; Nicolas Lartillot
Journal:  Mol Biol Evol       Date:  2007-09-21       Impact factor: 16.240

Review 5.  Rates of evolutionary change in viruses: patterns and determinants.

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6.  Bayesian hypothesis testing of four-taxon topologies using molecular sequence data.

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7.  Phylogeography takes a relaxed random walk in continuous space and time.

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Journal:  Mol Biol Evol       Date:  2010-03-04       Impact factor: 16.240

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Journal:  Mol Biol Evol       Date:  2010-04-02       Impact factor: 16.240

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  395 in total

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7.  Characterization of Colombian serotype 1 avian paramyxoviruses, 2008-2010.

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8.  Global phylogeography and evolutionary history of Shigella dysenteriae type 1.

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10.  Evolutionary dynamics of group A and B respiratory syncytial virus in China, 2009-2018.

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