Evidence map›Paper›PMID 41278937›Full record

ArticlebioRxiv : the preprint server for biology2025

SubCell: Proteome-aware vision foundation models for microscopy capture single-cell biology.

Ankit Gupta, Zoe Wefers, Konstantin Kahnert, Jan N Hansen, Mohini K Misra, Will Leineweber, Anthony Cesnik, Dan Lu, Ulrika Axelsson, Frederic Ballllosera and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Ankit GuptaScience for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0002-9961-1041
Zoe WefersBioengineering Department, Stanford University, Stanford, CA, USA.
Konstantin KahnertBioengineering Department, Stanford University, Stanford, CA, USA.ORCID 0000-0002-8454-4894
Jan N HansenScience for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0002-0489-7535
Mohini K MisraBioengineering Department, Stanford University, Stanford, CA, USA.
Will LeineweberBioengineering Department, Stanford University, Stanford, CA, USA.ORCID 0000-0003-3069-398X
Anthony CesnikBioengineering Department, Stanford University, Stanford, CA, USA.ORCID 0000-0002-5326-7134
Dan LuChan Zuckerberg Initiative, Redwood City, CA, USA.
Ulrika AxelssonScience for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0002-0273-9306
Frederic BalllloseraBioengineering Department, Stanford University, Stanford, CA, USA.
Russ B AltmanBioengineering Department, Stanford University, Stanford, CA, USA.ORCID 0000-0003-3859-2905
Theofanis KaraletsosChan Zuckerberg Initiative, Redwood City, CA, USA.
Emma LundbergScience for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0001-7034-0850

Funding

Bridge2AI: Cell Maps for AI (CM4AI) Data Generation ProjectOT2OD032742 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jean-Christophe Bélisle-Pipon, TIMOTHY W CLARK · 2022 to 2026
$21.5M
The Cancer Cell Map Initiative v2.0U54CA274502 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Nevan J Krogan · 2022 to 2026
$14.2M
Computational methods for characterizing sources of variability in drug responseR35GM153195 · NIGMS · STANFORD UNIVERSITY · PI RUSS BIAGIO ALTMAN · 2024 to 2026
$1.0M
NCI NIH HHS U54 CA274502NIGMS NIH HHS R35 GM153195NIH HHS OT2 OD032742
6 · The paper itself

Abstract

Cell morphology and subcellular protein organization provide important insights into cellular function and behavior. These features of cells can be studied using large-scale protein fluorescence microscopy, and machine learning has become a powerful tool to interpret the resulting images for biological insights. Here, we introduce SubCell, a suite of self-supervised deep learning models for fluorescence microscopy designed to accurately capture cellular morphology, protein localization, cellular organization, and biological function beyond what humans can readily perceive. These models were trained on the proteome-wide image collection from the Human Protein Atlas with a novel proteome-aware learning objective. SubCell outperforms state-of-the-art methods across a variety of tasks relevant to single-cell biology and generalizes to other fluorescence microscopy datasets without any fine-tuning. Additionally, we construct the first proteome-wide hierarchical map of proteome organization that is directly learned from image data. This vision-based multiscale cell map defines cellular subsystems with high resolution of protein complexes, reveals proteins with similar functions, and distinguishes dynamic and stable behaviors within cellular compartments. Finally, Subcell enables a rich multimodal protein representation when integrated with a protein sequence model, allowing for a more comprehensive capture of gene function than either vision-only or sequence-only models alone. In conclusion, SubCell creates deep, image-driven representations of cellular architecture that are applicable across diverse biological contexts and datasets.

Identifiers

PMID41278937
PMCPMC12636579

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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.