Evidence map›Paper›PMID 37821450›Full record

ArticleNature communications2023

Revealing invisible cell phenotypes with conditional generative modeling.

Alexis Lamiable, Tiphaine Champetier, Francesco Leonardi, Ethan Cohen, Peter Sommer, David Hardy, Nicolas Argy, Achille Massougbodji, Elaine Del Nery, Gilles Cottrell and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
11.1field-weighted citation impact, top 2% of its field
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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  8. bioRxiv : the preprint server for biology · 2025
    Article
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  11. Towards generative digital twins in biomedical research.Computational and structural biotechnology journal · 2024
    Review
  12. Article
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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

12 authors at 4 institutions in 2 countries.

Alexis Lamiable *Computational Bioimaging and Bioinformatics, Institut de Biologie de l'Ecole Normale Supérieure, PSL University, 46, rue d'Ulm, 75005, Paris, France.
Tiphaine Champetier *Computational Bioimaging and Bioinformatics, Institut de Biologie de l'Ecole Normale Supérieure, PSL University, 46, rue d'Ulm, 75005, Paris, France.
Francesco LeonardiComputational Bioimaging and Bioinformatics, Institut de Biologie de l'Ecole Normale Supérieure, PSL University, 46, rue d'Ulm, 75005, Paris, France.
Ethan CohenComputational Bioimaging and Bioinformatics, Institut de Biologie de l'Ecole Normale Supérieure, PSL University, 46, rue d'Ulm, 75005, Paris, France.ORCID http://orcid.org/0000-0002-5019-7759
Peter SommerKsilink, 16 rue d'Ankara, 67000, Strasbourg, France.ORCID http://orcid.org/0000-0001-9241-5710
David HardyHistopathology Platform, Institut Pasteur, F-75015, Paris, France.
Nicolas ArgyUniversité Paris-Cité, MERIT, IRD, F-75006, Paris, France.ORCID http://orcid.org/0000-0002-0458-2664
Achille MassougbodjiInstitut de Recherche Clinique du Bénin, Abomey-Calavi, Benin.
Elaine Del NeryBiophenics, Institut Curie, PSL Research University, Department of Translational Research, Cell and Tissue Imaging Facility (PICT-IBiSA), 26 rue d'Ulm, 75005, Paris, France.ORCID http://orcid.org/0000-0002-9654-5202
Gilles CottrellUniversité Paris-Cité, MERIT, IRD, F-75006, Paris, France.ORCID http://orcid.org/0000-0002-7964-8963
Yong-Jun KwonKsilink, 16 rue d'Ankara, 67000, Strasbourg, France. yong-jun.kwon@lih.lu.
Auguste GenovesioComputational Bioimaging and Bioinformatics, Institut de Biologie de l'Ecole Normale Supérieure, PSL University, 46, rue d'Ulm, 75005, Paris, France. auguste.genovesio@ens.psl.eu.ORCID http://orcid.org/0000-0003-1877-5595
Université Paris Sciences et Lettres · FRUniversité Paris Cité · FRInstitut Pasteur · FRLuxembourg Institute of Health · LU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biological sciences, drug discovery and medicine rely heavily on cell phenotype perturbation and microscope observation. However, most cellular phenotypic changes are subtle and thus hidden from us by natural cell variability: two cells in the same condition already look different. In this study, we show that conditional generative models can be used to transform an image of cells from any one condition to another, thus canceling cell variability. We visually and quantitatively validate that the principle of synthetic cell perturbation works on discernible cases. We then illustrate its effectiveness in displaying otherwise invisible cell phenotypes triggered by blood cells under parasite infection, or by the presence of a disease-causing pathological mutation in differentiated neurons derived from iPSCs, or by low concentration drug treatments. The proposed approach, easy to use and robust, opens the door to more accessible discovery of biological and disease biomarkers.

Indexed as

Induced Pluripotent Stem CellsCell DifferentiationDrug DiscoveryPhenotype

Identifiers

PMID37821450
PMCPMC10567685
OpenAlexW4387517389

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.