Evidence map›Paper›PMID 41967133›Full record

ArticleMolecular biology and evolution2026

Phylogenomic mixture models outperform homogeneous and partitioned models.

Davide Pisani, Mattia Giacomelli, Gergely J Szöllősi, Maria Eleonora Rossi, Marc Domènech, Jesus Lozano-Fernandez

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Davide PisaniBristol Palaeobiology Group, School of Biological Sciences, University of Bristol, Bristol BS8 1TH, UK.ORCID 0000-0003-0949-6682
Mattia GiacomelliDepartment de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona, Barcelona 08028, Spain.ORCID 0000-0002-0554-3704
Gergely J SzöllősiModel-Based Evolutionary Genomics Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan.ORCID 0000-0002-8556-845X
Maria Eleonora RossiCentre for Chromosome Biology, School of Biological and Chemical Sciences, University of Galway, Galway H91 W2TY, Ireland.ORCID 0000-0002-4076-5601
Marc DomènechDepartment de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona, Barcelona 08028, Spain.ORCID 0000-0003-4352-5301
Jesus Lozano-FernandezDepartment de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona, Barcelona 08028, Spain.ORCID 0000-0003-3597-1221

Funding

Comissió Interdepartamental de Recerca i Innovació Tecnològica 2021SGR00279European Union NextGenerationEU/PRTRJohn Templeton Foundation CNS2022-135805John Templeton Foundation Grant 63451John Templeton Foundation MICIU/AEI/10.13039/501100011033John Templeton Foundation PID2022-137753NA-I00Leverhulme Trust Research Project RPG-2024-030Margarita SalasMarie Skłodowska-Curie 101202964Marie Skłodowska-Curie HORIZON-MSCA-2024-PF-01Natural Environment Research Council NE/P013678/1Natural Science Foundation of ChinaNERC NE/L002434/1University of Bristol University Research Fellowship
6 · The paper itself

Abstract

Significant advances have been made in resolving the tree of life, but many nodes remain debated. The last two decades saw the emergence of mixture models, which proved particularly useful to account for across-site compositional heterogeneity, and played a central role to improve our understanding of difficult phylogenetic problems. However, some scholars have remained skeptical of their use. Here, we perform a large simulation study comparing mixture models accounting for across-site compositional heterogeneity, across-site compositionally homogeneous models and partitioned models. We show that the tested mixture models fit across-site compositionally heterogeneous datasets best and achieve greater accuracy. Of the tested models, CAT-GTR, an infinite mixture model combining a general time reversible-GTR-matrix with a mixture of site-frequency profiles (i.e. categories-CAT-or components) characterized by different amino acid frequency vectors, maximizes accuracy and fit. Mixture models, and particularly CAT-GTR, perform well also with across-site compositionally homogeneous datasets, where the use of a mixture of site-frequency profiles is not necessary. We show that this is because with homogeneous data these models converge to appropriate compositionally homogeneous models, avoiding overparametrization. Our results dissipate doubts about the utility of models accounting for compositional heterogeneity across sites and identify CAT-GTR as one of the most flexible models in the phylogenomic arsenal.

Indexed as

Models, GeneticPhylogenyComputer Simulationcompositional heterogeneitylong branch attractionmixture modelsmodel fitphylogenetic accuracysimulations

Identifiers

PMID41967133
PMCPMC13197666

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.