比例(比率)
染色质
计算机科学
地图学
生物
地理
遗传学
DNA
作者
Xiaoqing Wu,Zian Wang,Rui Jiang,Xiaoyang Chen
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-08-28
卷期号:12 (35): eaeg0134-eaeg0134
标识
DOI:10.1126/sciadv.aeg0134
摘要
Abstract Single-cell Hi-C captures the three-dimensional organization of chromatin in individual cells and provides insights into fundamental genomic processes such as gene regulation and transcription. While analyses of bulk Hi-C data have revealed multi-scale chromatin structures like A/B compartments and topologically associating domains, single-cell Hi-C data remain challenging to analyze due to sparsity and uneven distribution of chromatin contacts across genomic distances. These characteristics lead to strong signals near the diagonal and complex multi-scale local patterns in single-cell contact maps. Here, we propose Hi-Cformer, a transformer-based method that simultaneously models multi-scale blocks of chromatin contact maps and incorporates a specially designed attention mechanism to capture the dependencies between chromatin interactions across genomic regions and scales, enabling the integration of both global and fine-grained chromatin interaction features. Building on this architecture, Hi-Cformer robustly derives low-dimensional representations of cells from single-cell Hi-C data, achieving clearer separation of cell types compared to existing methods. Hi-Cformer can also accurately impute chromatin interaction signals associated with cellular heterogeneity, including 3D genome features such as topologically associating domain-like boundaries and A/B compartments. Furthermore, by leveraging its learned embeddings, Hi-Cformer can be extended to cell type annotation, achieving high accuracy and robustness across both intra- and inter-dataset scenarios.
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