Evidence map›Paper›PMID 41116016›Full record

ArticleNature methods2025

CELLECT: contrastive embedding learning for large-scale efficient cell tracking.

Hongyu Zhou, Seonghoon Kim, Zhifeng Zhao, Jiaqi Fan, Wen Huang, Xinghua Sui, Lizhi Shao, Haoran An, Jing-Ren Zhang, Jiamin Wu and 1 more

Abstract read
In one paragraph

Article in Nature methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Hongyu Zhou *Department of Automation, Tsinghua University, Beijing, China.ORCID http://orcid.org/0000-0003-1939-5922
Seonghoon Kim *Department of Automation, Tsinghua University, Beijing, China.ORCID http://orcid.org/0000-0002-1145-0336
Zhifeng ZhaoDepartment of Automation, Tsinghua University, Beijing, China.
Jiaqi FanDepartment of Automation, Tsinghua University, Beijing, China.ORCID http://orcid.org/0009-0001-1860-3729
Wen HuangDepartment of Automation, Tsinghua University, Beijing, China.
Xinghua SuiSchool of Pharmaceutical Sciences (Shenzhen), Shenzhen Campus of Sun Yat-sen University, Shenzhen, China.
Lizhi ShaoSchool of Internet, Anhui University, Hefei, China.ORCID http://orcid.org/0000-0002-8974-6540
Haoran AnInstitute of Medical Technology, Peking University Health Science Center, Beijing, China.
Jing-Ren ZhangCenter for Infectious Biology, School of Basic Medical Sciences, Tsinghua University, Beijing, China.
Jiamin WuDepartment of Automation, Tsinghua University, Beijing, China. wujiamin@tsinghua.edu.cn.ORCID http://orcid.org/0000-0003-3479-1026
Qionghai DaiDepartment of Automation, Tsinghua University, Beijing, China. qhdai@tsinghua.edu.cn.ORCID http://orcid.org/0000-0001-7043-3061

Funding

China Postdoctoral Science Foundation 2023M731985National Natural Science Foundation of China (National Science Foundation of China) 62088102National Natural Science Foundation of China (National Science Foundation of China) 62231018Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation) Z240011
6 · The paper itself

Abstract

Quantitative analysis of large-scale cellular behaviors plays an increasingly crucial role in understanding mechanisms of diverse physiopathological processes, but achieving cell tracking with both high performance and efficiency in practical applications remains a challenge. Here we introduce CELLECT, a contrastive embedding learning method for large-scale efficient cell tracking, and demonstrate it on the Caenorhabditis elegans dataset in the Cell Tracking Challenge. By contrastive learning of latent embeddings of diverse cellular structures, a CELLECT model pretrained on a single public dataset can be effectively applied across different imaging modalities and species with broad generalization. Using advanced two-photon imaging, CELLECT enables real-time 3D tracking of large-scale B cells with frequent divisions during germinal center formation in a mouse lymph node, quantitative identification of cell-bacterium interactions in the mouse spleen and high-fidelity extraction of neural signals during strong nonrigid motions. We believe that these results demonstrate broad applications of CELLECT in immunology, pathology and neuroscience.

Indexed as

Cell TrackingImage Processing, Computer-AssistedMachine LearningAlgorithmsAnimalsB-LymphocytesCaenorhabditis elegansGerminal CenterImaging, Three-DimensionalLymph NodesMiceSpleen

Identifiers

PMID41116016
PMCPMC12615263

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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.