Evidence map›Paper›PMID 42098097›Full record

ArticleNature communications2026

A versatile multi-components mixed model for bacterial-Genome Wide association studies.

Arthur Frouin, Fabien Laporte, Lukas Hafner, Mylène Maury, Zachary R McCaw, Hanna Julienne, Léo Henches, Alexandre Leclercq, Rayan Chikhi, Marc Lecuit and 1 more

Abstract read
In one paragraph

Article in Nature communications, 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

11 authors.

Arthur Frouin *Department of Computational Biology, USR 3756 CNRS, Institut Pasteur, Paris, France. arthurs.frouin@gmail.com.ORCID http://orcid.org/0000-0001-5237-0706
Fabien Laporte *Department of Computational Biology, USR 3756 CNRS, Institut Pasteur, Paris, France.
Lukas HafnerInstitut Pasteur, Université Paris Cité, Inserm U1117, Biology of Infection Unit, Paris, France.
Mylène MauryInstitut Pasteur, Université Paris Cité, Inserm U1117, Biology of Infection Unit, Paris, France.
Zachary R McCawInsitro, South San Francisco, California, USA.ORCID http://orcid.org/0000-0002-2006-9828
Hanna JulienneDepartment of Computational Biology, USR 3756 CNRS, Institut Pasteur, Paris, France.ORCID http://orcid.org/0000-0001-8214-9412
Léo HenchesDepartment of Computational Biology, USR 3756 CNRS, Institut Pasteur, Paris, France.
Alexandre LeclercqInstitut Pasteur, Université Paris Cité, Inserm U1117, Biology of Infection Unit, Paris, France.ORCID http://orcid.org/0000-0003-3778-7313
Rayan ChikhiDepartment of Computational Biology, USR 3756 CNRS, Institut Pasteur, Paris, France.ORCID http://orcid.org/0000-0003-1099-8735
Marc LecuitInstitut Pasteur, Université Paris Cité, Inserm U1117, Biology of Infection Unit, Paris, France.ORCID http://orcid.org/0000-0002-4491-1063
Hugues AschardDepartment of Computational Biology, USR 3756 CNRS, Institut Pasteur, Paris, France. hugues.aschard@pasteur.fr.ORCID http://orcid.org/0000-0002-7554-6783

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide Association Studies (GWAS) have played a crucial role in uncovering the genetics underlying complex human traits. Recently, there has been considerable interest in adapting GWAS-like methodologies to investigate pathogenic bacteria. Despite the variety of methods proposed, there remains a lack of clarity on how to effectively model the intricate population structures found in bacterial cohorts. In this study, we analyze the genetic architecture of whole-genome sequencing data from three distinct bacterial species, showing that the standard models used in human genetics, typically employed by existing bacterial GWAS methods, fall short when applied to organisms with highly structured genomes. Building on these findings, we introduce ChoruMM, a robust and powerful multi-component linear mixed model. This model infers components through hierarchical clustering of the bacterial genetic relatedness matrix. Extensive simulations show that our approach reduces false positives while maintaining, or even improving, detection rates compared to current pipelines. The ChoruMM package includes post-processing and visualization tools designed to address the prevalent issue of long-range correlations in bacterial genomes, enabling accurate assessment and calibration of type I error rates.

Indexed as

BacteriaGenome, BacterialGenome-Wide Association StudyModels, GeneticComputer SimulationHumansWhole Genome Sequencing

Identifiers

PMID42098097
PMCPMC13365456

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Registered trials

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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.