Evidence map›Paper›PMID 41942438›Full record

ArticleNature communications2026

CellLoop: Identifying single-cell 3D genome chromatin loops.

Yusen Ye, Yiheng Wang, Shiji Liu, Yuxuan Hu, Liang Yu, Weibing Wang, Shihua Zhang, Hebing Chen, Lin Gao

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

9 authors.

Yusen YeSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China. ysye@xidian.edu.cn.ORCID http://orcid.org/0000-0001-8687-1058
Yiheng WangSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Shiji LiuSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Yuxuan HuSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Liang YuSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Weibing WangSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China.
Shihua ZhangNCMIS, CEMS, RCSDS, Academy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, China.ORCID http://orcid.org/0000-0003-0192-7118
Hebing ChenAcademy of Military Medical Sciences, Beijing, China. chenhb@bmi.ac.cn.ORCID http://orcid.org/0000-0003-4102-356X
Lin GaoSchool of Computer Science and Technology, Xidian University, Xi'an, Shaanxi, China. lgao@mail.xidian.edu.cn.ORCID http://orcid.org/0000-0001-6396-0787

Funding

National Natural Science Foundation of China (National Science Foundation of China) 62002277National Natural Science Foundation of China (National Science Foundation of China) 62132015National Natural Science Foundation of China (National Science Foundation of China) 62350087National Natural Science Foundation of China (National Science Foundation of China) 62422318National Natural Science Foundation of China (National Science Foundation of China) 62550005National Natural Science Foundation of China (National Science Foundation of China) 62573335
6 · The paper itself

Abstract

Single-cell 3D genome technologies provide unprecedented views of chromatin architecture, but the extreme sparsity and noise of contact maps limit robust detection of chromatin loops at the individual cell level. Here we present CellLoop, a computational framework for identifying chromatin loops from single-cell contact data by integrating intra-cellular and neighboring inter-cellular contacts through a density-based voting strategy. Applied to Dip-C data from the mouse brain, CellLoop achieves improved loop detection consistent with spatial distances and compartmentalization signals, revealing single cell-specific chromatin loops associated with transcriptional regulation and cell identity. In HiRES embryogenesis data, CellLoop enables finer cell subtype delineation by reducing confounding cell cycle effects. Integration with GAGE-seq and MERFISH data redefines spatial domain functions through chromatin loop dynamics. Together, CellLoop provides a scalable and accurate approach for characterizing chromatin loop variability at single-cell resolution and highlights the utility of 3D genome features in interpreting transcriptional and spatial heterogeneity.

Indexed as

ChromatinGenomeSingle-Cell AnalysisAnimalsBrainMiceChromatin

Identifiers

PMID41942438
PMCPMC13230548

What OpenQuestion holds

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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.