Evidence map›Paper›PMID 41513659›Full record

ArticleNature communications2026

sCellST predicts single-cell gene expression from H& E images.

Loïc Chadoutaud, Marvin Lerousseau, Daniel Herrero-Saboya, Julian Ostermaier, Jacqueline Fontugne, Emmanuel Barillot, Thomas Walter

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. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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

7 authors.

Loïc ChadoutaudCentre for Computational Biology (CBIO), Mines Paris, PSL University, Paris, France.
Marvin LerousseauCentre for Computational Biology (CBIO), Mines Paris, PSL University, Paris, France.
Daniel Herrero-SaboyaCentre for Computational Biology (CBIO), Mines Paris, PSL University, Paris, France.ORCID http://orcid.org/0009-0001-9948-1531
Julian OstermaierCentre for Computational Biology (CBIO), Mines Paris, PSL University, Paris, France.
Jacqueline FontugneInstitut Curie, Department of Pathology, Saint-Cloud, France.
Emmanuel BarillotCentre for Computational Biology (CBIO), Mines Paris, PSL University, Paris, France. emmanuel.barillot@curie.fr.ORCID http://orcid.org/0000-0003-2724-2002
Thomas WalterCentre for Computational Biology (CBIO), Mines Paris, PSL University, Paris, France. thomas.walter@minesparis.psl.eu.ORCID http://orcid.org/0000-0001-7419-7879

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-19-P3IA-0001Agence Nationale de la Recherche (French National Research Agency) ANR-19-P3IA-0001 (PRAIRIE 3IA Institute)Agence Nationale de la Recherche (French National Research Agency) ANR-24-EXCI-0001, ANR-24-EXCI-0002, ANR-24-EXCI-0003, ANR-24-EXCI-0004, ANR-24-EXCI-0005Institut National Du Cancer (French National Cancer Institute) PRTK SELECT
6 · The paper itself

Abstract

Understanding the spatial organization of individual cell types within tissue and how this organization is disrupted in disease, is a central question in biology and medicine. Hematoxylin and eosin-stained slides are widely available and provide detailed morphological context, while spatial gene expression profiling offers complementary molecular insights, though it remains costly and limited in accessibility. Predicting gene expression directly from histological images is therefore an attractive goal. However, existing approaches typically rely on small image patches, limiting resolution and the ability to capture fine-grained morphological variation. Here, we introduce a deep learning approach that predicts single-cell gene expression from morphology, matching patch-based methods on spot level prediction tasks. The model recovers biologically meaningful expression patterns across two cancer datasets and distinguishes fine cell populations. This approach enables molecular-level interpretation of standard histological slides at scale, offering new opportunities to study tissue organization and cellular diversity in health and disease.

Indexed as

Gene Expression ProfilingImage Processing, Computer-AssistedSingle-Cell AnalysisDeep LearningHumansNeoplasmsSingle-Cell Gene Expression Analysis

Identifiers

PMID41513659
PMCPMC12858858

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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.