计算机科学
聚类分析
工作流程
层次聚类
仿形(计算机编程)
代表(政治)
数据可视化
数据挖掘
过程(计算)
生物学数据
降维
选择(遗传算法)
功能(生物学)
双聚类
生物细胞
计算生物学
超参数
交互式可视化
非线性降维
人工智能
图形
维数之咒
特征选择
生物信息学
可视化
生物网络
噪音(视频)
作者
Bingjie Li,Runyu Lin,Tianhao Ni,Guanao Yan,Mannix J. Burns,Jingyi Jessica Li,Zhigang Yao
标识
DOI:10.1038/s41467-025-67890-3
摘要
Single-cell sequencing enables comprehensive profiling of individual cells, revealing cellular heterogeneity and function with unprecedented resolution. However, current analysis frameworks lack the ability to simultaneously explore and visualize cellular hierarchies at multiple biological levels. To address these limitations, we present CellScope, a promising framework for constructing high-resolution cell atlases at multiple clustering levels. CellScope employs a two-stage manifold fitting process for gene selection and noise reduction, followed by agglomerative clustering, and integrates UMAP visualization with hierarchical clustering to intuitively represent cellular relationships simultaneously at multiple levels—such as cell lineage, cell type, and cell subtype levels. Compared to established pipelines such as Seurat and Scanpy, CellScope comprehensively improves clustering performance, visualization clarity, computational efficiency, and algorithm interpretability, while reducing dependence on hyperparameters across a multitude of single-cell datasets. Most importantly, it can reveal biological insights that other contemporary methods are unable to detect, thereby deepening our understanding of cellular heterogeneity and function, and potentially informing disease research. Li and colleagues present CellScope, a tree-structured framework that reveals multi-level cellular hierarchies and gene functions in single-cell data. This approach provides clear clustering, intuitive visualization, and deep biological views into cell types and functions.
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