RMDisease V2.0: an updated database of genetic variants that affect RNA modifications with disease and trait implication

Recent advances in epitranscriptomics have unveiled functional associations between RNA modifications (RMs) and multiple human diseases, but distinguishing the functional or disease-related single nucleotide variants (SNVs) from the majority of 'silent' variants remains a major challenge....

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Veröffentlicht in:Nucleic acids research 2023-01, Vol.51 (D1), p.D1388-D1396
Hauptverfasser: Song, Bowen, Wang, Xuan, Liang, Zhanmin, Ma, Jiongming, Huang, Daiyun, Wang, Yue, de Magalhães, João Pedro, Rigden, Daniel J, Meng, Jia, Liu, Gang, Chen, Kunqi, Wei, Zhen
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Sprache:eng
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