Evidence map›Paper›PMID 41839876›Full record

ArticleNature communications2026

Illuminating cell states by a comprehensive and interpretable single cell foundation model.

Jue Wang, Cheng Tan, Zhangyang Gao, Sida Shao, Shiping Liu, Stan Z Li

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 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

6 authors.

Jue Wang *Zhejiang University, Hangzhou, China.ORCID http://orcid.org/0009-0006-4270-2387
Cheng Tan *Zhejiang University, Hangzhou, China.
Zhangyang GaoZhejiang University, Hangzhou, China.
Sida ShaoWestlake University, Hangzhou, China.
Shiping LiuBGI Research, Hangzhou, China. liushiping@genomics.cn.ORCID http://orcid.org/0000-0003-0019-619X
Stan Z LiWestlake University, Hangzhou, China. Stan.ZQ.Li@westlake.edu.cn.ORCID http://orcid.org/0000-0002-2961-8096

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in single-cell sequencing have enabled AI-driven foundation models with powerful data representation. However, their practical use is limited by real-world data sparsity, heterogeneity, and poor interpretability. To overcome these, we introduce CellVQ. To enhance generalizability, we incorporate a large-scale single-cell dataset comprising 68 million cells, model parameters totaling 500 million, and challenging pretraining tasks. Notably, we introduce a Single-Cell Discretization (SCD) module that effectively represents cell embeddings, addressing data heterogeneity. For improved interpretability, the SCD module transforms high-dimensional and sparse single-cell data into a "cell code," facilitating recognition and analysis. Additionally, we also present CellVQ-Graph, a plug-and-play tool that integrates CellVQ's features with multimodal data (genes, cell communication, annotations) to build a knowledge graph for biological discovery. Extensively evaluated, CellVQ outperforms strong baselines in all downstream tasks, and also uncovered intriguing biological phenomena with compelling explanations. CellVQ aspires to serve as a truly applicable and generalizable AI tool for the cell biology community.

Indexed as

Computational BiologySingle-Cell AnalysisAnimalsHumansModels, BiologicalSoftware

Identifiers

PMID41839876
PMCPMC13139411

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.