计算机科学
弹道
系统生物学
聚类分析
计算生物学
约束(计算机辅助设计)
软件
基因调控网络
生物
分布式计算
人工智能
基因
基因表达
遗传学
工程类
机械工程
物理
程序设计语言
天文
作者
Alexander G. B. Grønning,Mhaned Oubounyt,Kristiyan Kanev,Jesper Lund,Tim Kacprowski,Dietmar Zehn,Richard Röttger,Jan Baumbach
标识
DOI:10.1038/s43588-021-00025-y
摘要
Single-cell sequencing (scRNA-seq) technologies allow the investigation of cellular differentiation processes with unprecedented resolution. Although powerful software packages for scRNA-seq data analysis exist, systems biology-based tools for trajectory analysis are rare and typically difficult to handle. This hampers biological exploration and prevents researchers from gaining deeper insights into the molecular control of developmental processes. Here, to address this, we have developed Scellnetor; a network-constraint time-series clustering algorithm. It allows extraction of temporal differential gene expression network patterns (modules) that explain the difference in regulation of two developmental trajectories. Using well-characterized experimental model systems, we demonstrate the capacity of Scellnetor as a hypothesis generator to identify putative mechanisms driving haematopoiesis or mechanistically interpretable subnetworks driving dysfunctional CD8 T-cell development in chronic infections. Altogether, Scellnetor allows for single-cell trajectory network enrichment, which effectively lifts scRNA-seq data analysis to a systems biology level. Scellnetor is a single-cell network enrichment method that can unravel connected molecular interaction networks to explain the progression and differentiation of developmental trajectories on a systems biology level.
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