ArticleNature communications2026
A versatile multi-components mixed model for bacterial-Genome Wide association studies.
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.