Evidence map›Paper›PMID 34498586›Full record

ArticleeLife2021

Misic, a general deep learning-based method for the high-throughput cell segmentation of complex bacterial communities.

Swapnesh Panigrahi, Dorothée Murat, Antoine Le Gall, Eugénie Martineau, Kelly Goldlust, Jean-Bernard Fiche, Sara Rombouts, Marcelo Nöllmann, Leon Espinosa, Tâm Mignot

Abstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  5. Biofilms: from the cradle of life to life support.NPJ biofilms and microbiomes · 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

10 authors.

Swapnesh PanigrahiCNRS-Aix-Marseille University, Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée and Turing Center for Living Systems, Marseille, France.
Dorothée MuratCNRS-Aix-Marseille University, Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée and Turing Center for Living Systems, Marseille, France.ORCID 0000-0001-5809-9267
Antoine Le GallCentre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, Université de Montpellie, Marseille, France.
Eugénie MartineauCNRS-Aix-Marseille University, Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée and Turing Center for Living Systems, Marseille, France.
Kelly GoldlustCNRS-Aix-Marseille University, Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée and Turing Center for Living Systems, Marseille, France.
Jean-Bernard FicheCentre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, Université de Montpellie, Marseille, France.
Sara RomboutsCentre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, Université de Montpellie, Marseille, France.
Marcelo NöllmannCentre de Biochimie Structurale, CNRS UMR 5048, INSERM U1054, Université de Montpellie, Marseille, France.
Leon EspinosaCNRS-Aix-Marseille University, Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée and Turing Center for Living Systems, Marseille, France.ORCID 0000-0002-1923-2069
Tâm MignotCNRS-Aix-Marseille University, Laboratoire de Chimie Bactérienne, Institut de Microbiologie de la Méditerranée and Turing Center for Living Systems, Marseille, France.ORCID 0000-0003-4338-9063

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Studies of bacterial communities, biofilms and microbiomes, are multiplying due to their impact on health and ecology. Live imaging of microbial communities requires new tools for the robust identification of bacterial cells in dense and often inter-species populations, sometimes over very large scales. Here, we developed MiSiC, a general deep-learning-based 2D segmentation method that automatically segments single bacteria in complex images of interacting bacterial communities with very little parameter adjustment, independent of the microscopy settings and imaging modality. Using a bacterial predator-prey interaction model, we demonstrate that MiSiC enables the analysis of interspecies interactions, resolving processes at subcellular scales and discriminating between species in millimeter size datasets. The simple implementation of MiSiC and the relatively low need in computing power make its use broadly accessible to fields interested in bacterial interactions and cell biology.

Indexed as

Bacterial Physiological PhenomenaDeep LearningMicrobiotaModels, BiologicalBiofilmsHigh-Throughput Screening AssaysMicroscopySpecies SpecificitybiofilmsB. subtiliscomputational biologyDeep learningE. coliimage analysisinfectious diseasemicrobiologymicroscopymyxococcus xanthussystems biology

Identifiers

PMID34498586
PMCPMC8478410

What OpenQuestion holds

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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.