Partitionfinder: combined selection of partitioning schemes and substitution models for phylogenetic analyses

Robert Lanfear, Brett Calcott, Simon Y. W. Ho, Stephane Guindon

Research output: Contribution to journalArticlepeer-review

3781 Citations (Scopus)


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
Original languageEnglish
Pages (from-to)1695-1701
Number of pages7
JournalMolecular Biology and Evolution
Issue number6
Publication statusPublished - 2012
Externally publishedYes


  • Partitioning
  • AIC
  • BIC
  • AICc
  • Model selection
  • Molecular evolution

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