PanCan-scEditome

Welcome to PanCan-scEditome, an interactive analysis platform and database dedicated to the single-cell and long-read RNA editing landscape across human cancers.

PanCan-scEditome integrates long-read sequencing and single-cell RNA sequencing to provide a high-resolution, pan-cancer atlas of RNA editing events. By leveraging the unique structural properties of long-read data, we perform de novo identification of editing sites without requiring matched genomic DNA, and project these profiles across large cell populations. Through a standardized analytical framework, users can easily browse, search, and perform customized analyses.