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

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 editi...

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Detalles Bibliográficos
Autores principales: Chen, Longxian, Ou, Liang, Jing, Xinyun, Kong, Yimeng, Xie, Bingran, Zhang, Niubing, Shi, Han, Qin, Hang, Li, Xuan, Hao, Pei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108526/
https://www.ncbi.nlm.nih.gov/pubmed/37069604
http://dx.doi.org/10.1186/s13059-023-02921-0
Descripción
Sumario: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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13059-023-02921-0.