Wang Yajunzi, Li Jing, Zha Haoruo, Liu Shuhe, Huang Daiyun, Fu Lei, Liu Xin
Wisdom Lake Academy of Pharmacy, Xi'an Jiaotong-Liverpool University, 111 Ren'ai Road, Suzhou Industrial Park, Suzhou, Jiangsu 215123, China.
Institute of Systems, Molecular and Integrative Biology, University of Liverpool, Biosciences Building, Crown Street, Liverpool L69 7ZX, United Kingdom.
Brief Bioinform. 2025 Jul 2;26(4). doi: 10.1093/bib/bbaf339.
Single-cell RNA sequencing enables unprecedented insights into cellular heterogeneity and lineage dynamics. RNA velocity, by modeling the temporal relationship between spliced and unspliced transcripts, extends this capability to predict future transcriptional states and uncover the directionality of cellular transitions. Since the introduction of foundational frameworks such as Velocyto and scVelo, an expanding array of computational tools has emerged, each based on distinct biophysical assumptions and modeling paradigms. To provide a structured overview of this rapidly evolving field, we categorize RNA velocity models into three classes: steady-state methods, trajectory methods, and state extrapolation methods, according to their underlying approaches to transcriptional kinetics inference. For each category, we systematically analyze both the overarching principles and the individual methods, comparing their assumptions, kinetic models, and computational strategies and assessing their respective strengths and limitations. To demonstrate the biological utility of these tools, we summarize representative applications of RNA velocity across developmental biology and diseased microenvironments. We further introduce emerging extensions of RNA velocity methods that go beyond classical splicing kinetics. Finally, we discuss existing limitations regarding model assumptions, preprocessing procedures, and velocity visualization and offer practical recommendations for model selection and application. This review offers a comprehensive guide to the RNA velocity landscape, supporting its effective implementation in dynamic transcriptomic research.
单细胞RNA测序能够以前所未有的方式洞察细胞异质性和谱系动态。通过对剪接和未剪接转录本之间的时间关系进行建模,RNA速度将这一能力扩展到预测未来转录状态并揭示细胞转变的方向性。自从引入诸如Velocyto和scVelo等基础框架以来,出现了越来越多的计算工具,每个工具都基于不同的生物物理假设和建模范式。为了对这个快速发展的领域进行结构化概述,我们根据其转录动力学推断的潜在方法,将RNA速度模型分为三类:稳态方法、轨迹方法和状态外推方法。对于每一类,我们系统地分析总体原理和各个方法,比较它们的假设、动力学模型和计算策略,并评估它们各自的优势和局限性。为了展示这些工具的生物学实用性,我们总结了RNA速度在发育生物学和患病微环境中的代表性应用。我们还介绍了超越经典剪接动力学的RNA速度方法的新兴扩展。最后,我们讨论了关于模型假设、预处理程序和速度可视化的现有局限性,并为模型选择和应用提供了实用建议。本综述为RNA速度领域提供了全面指南,支持其在动态转录组学研究中的有效实施。