LncAS2Cancer

LncAS2Cancer aims to present comprehensive view of lncRNA splicing across human cancers. Totally, 50,859/151,216 splicing events of 4,155/9,316 lncRNAs in GENCODE/FANTOM among over 30 cancer types are deposited, incorporating 5,335 samples for bulk RNA sequencing and 1,826 samples for smart-based single-cell RNA sequencing.LncAS2Cancer 旨在全面呈现人类癌症中长链非编码RNA（long non-coding RNA, lncRNA）的可变剪接全貌。本数据集共收录了覆盖30余种癌症类型的相关数据：包含GENCODE与FANTOM数据库中4155/9316条长链非编码RNA对应的50859/151216个剪接事件，其中批量RNA测序样本共5335例，基于Smart技术的单细胞RNA测序样本共1826例。