Evidence map›Paper›PMID 38517978›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Modeling the mosaic structure of bacterial genomes to infer their evolutionary history.

Michael Sheinman, Peter F Arndt, Florian Massip

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Michael SheinmanInstitute for Advanced Studies, Sevastopol State University, Sevastopol 299053, Crimea.ORCID 0000-0002-3717-1722
Peter F ArndtDepartment of Computational Molecular Biology, Max Planck Institute for Molecular Genetics, Berlin 12163, Germany.ORCID 0000-0003-1762-9836
Florian MassipDepartment U900, Centre for Computational Biology, Mines Paris, PSL University, Paris 75006, France.ORCID 0000-0001-5855-0935

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chronology and phylogeny of bacterial evolution are difficult to reconstruct due to a scarce fossil record. The analysis of bacterial genomes remains challenging because of large sequence divergence, the plasticity of bacterial genomes due to frequent gene loss, horizontal gene transfer, and differences in selective pressure from one locus to another. Therefore, taking advantage of the rich and rapidly accumulating genomic data requires accurate modeling of genome evolution. An important technical consideration is that loci with high effective mutation rates may diverge beyond the detection limit of the alignment algorithms used, biasing the genome-wide divergence estimates toward smaller divergences. In this article, we propose a novel method to gain insight into bacterial evolution based on statistical properties of genome comparisons. We find that the length distribution of sequence matches is shaped by the effective mutation rates of different loci, by the horizontal transfers, and by the aligner sensitivity. Based on these inputs, we build a model and show that it accounts for the empirically observed distributions, taking the

Indexed as

Genome, BacterialModels, GeneticBacteriaEvolution, MolecularGenomicsPhylogenybacterial evolutionhorizontal gene transfermaximal exact matchesmolecular clockmutation rate

Identifiers

PMID38517978
PMCPMC10990148

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.