ArticleNature communications2026
CellLoop: Identifying single-cell 3D genome chromatin loops.
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.
What it found
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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
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Who cites it
1 citing paper in PubMed.
- CellLoop: Identifying single-cell 3D genome chromatin loops.Nature communications · 2026Article
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Authors and funding
9 authors.
Funding
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.
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Registered trials
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