Cited by 5,732Genomics and Phylogenetic StudiesGenetic diversity and population structureEvolution and Paleontology Studies

PartitionFinder: Combined Selection of Partitioning Schemes and Substitution Models for Phylogenetic Analyses

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Lanfear, R., Calcott, B., Ho, S. Y. W., Guindon, S.·2012·Molecular Biology and Evolution

Abstract

In phylogenetic analyses of molecular sequence data, partitioning involves estimating independent models of molecular evolution for different sets of sites in a sequence alignment. Choosing an appropriate partitioning scheme is an important step in most analyses because it can affect the accuracy of phylogenetic reconstruction. Despite this, partitioning schemes are often chosen without explicit statistical justification. Here, we describe two new objective methods for the combined selection of best-fit partitioning schemes and nucleotide substitution models. These methods allow millions of partitioning schemes to be compared in realistic time frames and so permit the objective selection of partitioning schemes even for large multilocus DNA data sets. We demonstrate that these methods significantly outperform previous approaches, including both the ad hoc selection of partitioning schemes (e.g., partitioning by gene or codon position) and a recently proposed hierarchical clustering method. We have implemented these methods in an open-source program, PartitionFinder. This program allows users to select partitioning schemes and substitution models using a range of information-theoretic metrics (e.g., the Bayesian information criterion, akaike information criterion [AIC], and corrected AIC). We hope that PartitionFinder will encourage the objective selection of partitioning schemes and thus lead to improvements in phylogenetic analyses. PartitionFinder is written in Python and runs under Mac OSX 10.4 and above. The program, source code, and a detailed manual are freely available from www.robertlanfear.com/partitionfinder.

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  1. Jayaswal V, Ababneh F, Jermiin LS, Robinson J. Reducing model complexity of the general Markov model of evolution. Mol Biol Evol. Advance Access published May 18, 2011, doi:10.1093/molbev/ msr128 · DOI

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Authors
Lanfear, R., Calcott, B., Ho, S. Y. W., & Guindon, S.
Affiliations
  • Australian National University (AU)
  • The University of Sydney (AU)
  • University of Auckland (NZ)
Corresponding author
Lanfear, R.
Venue
Molecular Biology and Evolution
Published
2012-01-20
Volume
29
Issue
6
Pages
1695-1701
ISSN
  • 0737-4038 (ISSN-L)
  • 1537-1719
OpenAlex
W2133870991
Cited by
5,732
References
1
Citations by year
2026: 128 · 2025: 221 · 2024: 276 · 2023: 293 · 2022: 376 · 2021: 514 · 2020: 530 · 2019: 548 · 2018: 662 · 2017: 705 · 2016: 608 · 2015: 429 · 2014: 307 · 2013: 120 · 2012: 10
FWCI
111.25
Type
journal article
Language
en
Open access
Locations
  • Molecular Biology and Evolution (publishedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, cc-by)
  • ANU Open Research (Australian National University) (submittedVersion)
Funders
Marsden Fund (08-UOA-068)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic diversity and population structure
  • Physical Sciences › Earth and Planetary Sciences › Paleontology › Evolution and Paleontology Studies
Keywords
PartitionFinder, partitioning schemes, nucleotide substitution models, model selection, molecular evolution, phylogenetic inference, information-theoretic metrics, Bayesian information criterion, Akaike information criterion
MeSH terms
Algorithms, Bayes Theorem, Models, Genetic, Phylogeny, Selection, Genetic, Software, Cluster Analysis, Likelihood Functions, Sequence Analysis, DNA, Evolution, Molecular

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