Abstract
Understanding the temporal dynamics of gene expression within spatial contexts is essential for deciphering cellular differentiation. RNA velocity, which estimates the future state of gene expression by distinguishing spliced from unspliced mRNA, offers a powerful tool for studying these dynamics. However, current spatial transcriptomics technologies face limitations in simultaneously capturing both spliced and unspliced transcripts at high resolution. To address this challenge, a novel computational framework called KSRV (Kernel PCA-based Spatial RNA Velocity) that integrates single-cell RNA-seq with spatial transcriptomics using Kernel Principal Component Analysis. It enables accurately inference of RNA velocity in spatially resolved tissue at single-cell resolution. KSRV was validated by using 10x Visium data and MERFISH datasets. The results demonstrate its both accuracy and robustness comparing with the existed method such as SIRV and spVelo. Furthermore, KSRV successfully revealed spatial differentiation trajectories in the mouse brain and during mouse organogenesis, highlighting its potential for advancing our understanding of spatially dynamic biological processes.