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Updated: Sep 16, 2026

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
Published on: March 7, 2018
Comprehensive RNA velocity by modeling the cascade of gene regulation, transcription, and splicing from single-cell
Jiachen Li1, Zhe Wang1, Hong-Bin Shen2
1State Key Laboratory of Biopharmaceutical Preparation and Delivery, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, China.
Abstract:
RNA velocity approaches fit gene dynamics and infer cell fate by modeling the splicing process using single-cell RNA sequencing (scRNA-seq) data. However, due to the short time scale of splicing, high noise, and large complexity of data, existing RNA velocity methods often fail to precisely capture the complex velocity dynamics for individual genes and single cells, which makes their downstream analysis less reliable and less robust. We propose TSvelo, a comprehensive RNA velocity mathematics framework that can model the cascade of gene regulation, Transcription and Splicing using highly interpretable neural ordinary differential equations. TSvelo can precisely capture the transcription-unspliced-spliced 3D dynamics of all genes simultaneously, infer unified latent time shared by genes within a single cell, and be applied to multi-lineage datasets. Experiments on six scRNA-seq datasets, including two multi-lineage datasets, demonstrate TSvelo's superiority.
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