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DeepEdit:利用纳米孔直接 RNA 测序进行 A-to-I RNA 编辑事件的单分子检测和相位分析。

DeepEdit: single-molecule detection and phasing of A-to-I RNA editing events using nanopore direct RNA sequencing.

机构信息

Key Laboratory of Synthetic Biology, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, China.

Key Laboratory of Molecular Virology and Immunology, Institut Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, China.

出版信息

Genome Biol. 2023 Apr 17;24(1):75. doi: 10.1186/s13059-023-02921-0.

Abstract

Single-molecule detection and phasing of A-to-I RNA editing events remain an unresolved problem. Long-read and PCR-free nanopore native RNA sequencing offers a great opportunity for direct RNA editing detection. Here, we develop a neural network model, DeepEdit, that not only recognizes A-to-I editing events in single reads of Oxford Nanopore direct RNA sequencing, but also resolves the phasing of RNA editing events on transcripts. We illustrate the robustness of DeepEdit by applying it to Schizosaccharomyces pombe and Homo sapiens transcriptome data. We anticipate DeepEdit to be a powerful tool for the study of RNA editing from a new perspective.

摘要

单分子检测和 A-to-I RNA 编辑事件的相位仍然是一个未解决的问题。长读长和无 PCR 纳米孔天然 RNA 测序为直接 RNA 编辑检测提供了极好的机会。在这里,我们开发了一个神经网络模型 DeepEdit,它不仅可以识别牛津纳米孔直接 RNA 测序中单读的 A-to-I 编辑事件,还可以解析转录本上 RNA 编辑事件的相位。我们将 DeepEdit 应用于酿酒酵母和人类转录组数据,说明了其鲁棒性。我们预计 DeepEdit 将成为从新视角研究 RNA 编辑的有力工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a8f/10108526/35a4f540ce12/13059_2023_2921_Fig1_HTML.jpg

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