生物
核糖核酸
计算生物学
人类遗传学
DNA测序
遗传学
深度测序
RNA编辑
基因组生物学
DNA
基因组学
基因组
基因
作者
Zhi-Can Fu,Bao‐Qing Gao,Nan Fang,Xu-Kai Ma,Li Yang
标识
DOI:10.1186/s13059-024-03397-2
摘要
Precise calling of promiscuous adenosine-to-inosine RNA editing sites from transcriptomic datasets is hindered by DNA mutations and sequencing/mapping errors. Here, we present a stepwise computational framework, called DEMINING, to distinguish RNA editing and DNA mutations directly from RNA sequencing datasets, with an embedded deep learning model named DeepDDR. After transfer learning, DEMINING can also classify RNA editing sites and DNA mutations from non-primate sequencing samples. When applied in samples from acute myeloid leukemia patients, DEMINING uncovers previously underappreciated DNA mutation and RNA editing sites; some associated with the upregulated expression of host genes or the production of neoantigens. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-024-03397-2.
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