ArticleNature methods2025
CELLECT: contrastive embedding learning for large-scale efficient cell tracking.
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.
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.
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.
Who cites it
2 citing papers in PubMed.
- LFCT: A Benchmark Dataset for Low-Frame-Rate Cell Tracking in Long-Term Live-Cell Microscopy.bioRxiv : the preprint server for biology · 2026Article
- High-Fidelity Long-term Whole-embryo Lineage and Fate Reconstruction by Iterative Tracking with Error Correction.bioRxiv : the preprint server for biology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
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
Identifiers
What OpenQuestion holds
Registered trials
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.