弹道
核糖核酸
推论
计算生物学
人口
生物
基因表达
RNA剪接
计算机科学
表达式(计算机科学)
基因
遗传学
人工智能
物理
社会学
人口学
程序设计语言
天文
作者
Philipp Weiler,Koen Van Den Berge,Kelly Street,Simone Tiberi
出处
期刊:Methods in molecular biology
日期:2022-12-11
卷期号:: 269-292
被引量:10
标识
DOI:10.1007/978-1-0716-2756-3_14
摘要
Technological developments have led to an explosion of high-throughput single-cell data, which are revealing unprecedented perspectives on cell identity. Recently, significant attention has focused on investigating, from single-cell RNA-sequencing (scRNA-seq) data, cellular dynamic processes, such as cell differentiation, cell cycle and cell (de)activation. In particular, trajectory inference methods, by ordering cells along a trajectory, allow estimating a differentiation tree of cells. While trajectory inference tools typically work with gene expression levels, common scRNA-seq protocols allow the identification and quantification of unspliced pre-mRNAs and mature spliced mRNAs for each gene. By exploiting the abundance of unspliced and spliced mRNA, one can infer the RNA velocity of individual cells, i.e., the time derivative of the gene expression state of cells. Whereas traditional trajectory inference methods reconstruct cellular dynamics given a population of cells of varying maturity, RNA velocity relies on a dynamical model describing splicing dynamics. Here, we initially discuss conceptual and theoretical aspects of both approaches, then illustrate how they can be combined together, and finally present an example use case on real data.
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