Evidence map›Paper›PMID 40393991›Full record

ArticleNature communications2025

CellFM: a large-scale foundation model pre-trained on transcriptomics of 100 million human cells.

Yuansong Zeng, Jiancong Xie, Ningyuan Shangguan, Zhuoyi Wei, Wenbing Li, Yun Su, Shuangyu Yang, Chengyang Zhang, Jinbo Zhang, Nan Fang and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
–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

50 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  6. Unified representation learning for spatial multi-omics.Bioinformatics (Oxford, England) · 2026
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  20. Computational modelling of cell identity.The Biochemical journal · 2026
    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

16 authors.

Yuansong Zeng *School of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China. zengys@cqu.edu.cn.ORCID http://orcid.org/0009-0003-6470-0671
Jiancong Xie *School of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Ningyuan ShangguanSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Zhuoyi Wei *School of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Wenbing LiSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Yun SuHuawei Technologies Co., Ltd, Shenzhen, China.
Shuangyu YangDepartment of Medical Research Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China.
Chengyang ZhangSchool of Big Data and Software Engineering, Chongqing University, Chongqing, China.
Jinbo ZhangSingleron Biotechnologies, Nanjing, Jiangsu, China.
Nan FangSingleron Biotechnologies, Nanjing, Jiangsu, China.ORCID http://orcid.org/0000-0001-6234-8932
Hongyu ZhangSchool of Big Data and Software Engineering, Chongqing University, Chongqing, China.ORCID http://orcid.org/0000-0002-3063-9425
Yutong LuSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China.ORCID http://orcid.org/0000-0001-5315-3375
Huiying ZhaoDepartment of Medical Research Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China. zhaohy8@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0001-9134-536X
Jue FanSingleron Biotechnologies, Nanjing, Jiangsu, China. fanjue@singleronbio.com.ORCID http://orcid.org/0000-0002-6755-8258
Weijiang YuSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China. weijiangyu8@gmail.com.ORCID http://orcid.org/0000-0002-7449-3093
Yuedong YangSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China. yangyd25@mail.sysu.edu.cn.ORCID http://orcid.org/0000-0002-6782-2813

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell sequencing provides transcriptomic profiling at single-cell resolution, uncovering cellular heterogeneity with unprecedented precision. Yet, current single cell data analysis suffers from the inherent data noises, batch effects, and sparsity, highlighting the requirement of a unified model to represent cellular states. To circumvent this problem, many recent efforts focus on training single-cell foundation models based on large datasets. However, current human foundation models are still limited by the sizes of training data and model parameters. Here, we have collected a diverse dataset of 100 million human cells, on which we train a single-cell foundation model (CellFM) containing 800 million parameters. To balance efficiency and performance, the model is trained through a modified RetNet framework on the MindSpore. Extensive experiments have shown that CellFM outperforms existing models in cell annotation, perturbation prediction, gene function prediction, and gene-gene relationship capturing.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisTranscriptomeComputational BiologyHumans

Identifiers

PMID40393991
PMCPMC12092794

What OpenQuestion holds

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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.