生物
计算生物学
表型
效力
细胞
等级制度
疾病
细胞分化
特征(语言学)
电池类型
遗传学
基因
体外
医学
病理
哲学
经济
语言学
市场经济
作者
Minji Kang,José Juan Almagro Armenteros,Gunsagar S. Gulati,Rachel Gleyzer,Susanna Avagyan,Erin L. Brown,Wubing Zhang,Abul Usmani,Noah Earland,Zhenqin Wu,James Zou,Ryan C. Fields,David Y. Chen,Aadel A. Chaudhuri,Aaron M. Newman
标识
DOI:10.1101/2024.03.19.585637
摘要
Single-cell RNA sequencing (scRNA-seq) has transformed our understanding of cell fate in developmental systems. However, identifying the molecular hallmarks of potency - the capacity of a cell to differentiate into other cell types - has remained challenging. Here, we introduce CytoTRACE 2, an interpretable deep learning framework for characterizing potency and differentiation states on an absolute scale from scRNA-seq data. Across 31 human and mouse scRNA-seq datasets encompassing 28 tissue types, CytoTRACE 2 outperformed existing methods for recovering experimentally determined potency levels and differentiation states covering the entire range of cellular ontogeny. Moreover, it reconstructed the temporal hierarchy of mouse embryogenesis across 62 timepoints; identified pan-tissue expression programs that discriminate major potency levels; and facilitated discovery of cellular phenotypes in cancer linked to survival and immunotherapy resistance. Our results illuminate a fundamental feature of cell biology and provide a broadly applicable platform for delineating single-cell differentiation landscapes in health and disease.
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