Evidence map›Paper›PMID 39715360›Full record

ArticleMolecular biology and evolution2025

MixtureFinder: Estimating DNA Mixture Models for Phylogenetic Analyses.

Huaiyan Ren, Thomas K F Wong, Bui Quang Minh, Robert Lanfear

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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  6. Characterization ofViruses · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Huaiyan RenSchool of Computing, College of Engineering, Computing and Cybernetics, Australian National University, Canberra, ACT 2600, Australia.ORCID 0009-0009-2870-3481
Thomas K F WongSchool of Computing, College of Engineering, Computing and Cybernetics, Australian National University, Canberra, ACT 2600, Australia.ORCID 0000-0002-0580-6324
Bui Quang MinhSchool of Computing, College of Engineering, Computing and Cybernetics, Australian National University, Canberra, ACT 2600, Australia.ORCID 0000-0002-5535-6560
Robert LanfearEcology and Evolution, Research School of Biology, College of Science, Australian National University, Canberra, ACT 2600, Australia.ORCID 0000-0002-1140-2596

Funding

Australian Research Council DP200103151
6 · The paper itself

Abstract

In phylogenetic studies, both partitioned models and mixture models are used to account for heterogeneity in molecular evolution among the sites of DNA sequence alignments. Partitioned models require the user to specify the grouping of sites into subsets, and then assume that each subset of sites can be modeled by a single common process. Mixture models do not require users to prespecify subsets of sites, and instead calculate the likelihood of every site under every model, while co-estimating the model weights and parameters. While much research has gone into the optimization of partitioned models by merging user-specified subsets, there has been less attention paid to the optimization of mixture models for DNA sequence alignments. In this study, we first ask whether a key assumption of partitioned models-that each user-specified subset can be modeled by a single common process-is supported by the data. Having shown that this is not the case, we then design, implement, test, and apply an algorithm, MixtureFinder, to select the optimum number of classes for a mixture model of Q-matrices for the standard models of DNA sequence evolution. We show this algorithm performs well on simulated and empirical datasets and suggest that it may be useful for future empirical studies. MixtureFinder is available in IQ-TREE2, and a tutorial for using MixtureFinder can be found here: http://www.iqtree.org/doc/Complex-Models#mixture-models.

Indexed as

AlgorithmsModels, GeneticPhylogenyEvolution, MolecularSequence AlignmentSequence Analysis, DNASoftwaremixture modelmolecular evolutionphylogenetics

Identifiers

PMID39715360
PMCPMC11704958

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.