iMRM: a platform for simultaneously identifying multiple kinds of RNA modifications

被引:131
作者
Liu, Kewei [1 ]
Chen, Wei [1 ,2 ]
机构
[1] North China Univ Sci & Technol, Sch Life Sci, Ctr Genom & Computat Biol, Tangshan 063009, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, Innovat Inst Chinese Med & Pharm, Chengdu 611137, Peoples R China
关键词
WEB SERVER; MAPPING REVEALS; METHYLATION; ADENOSINE; NSUN2; 5-METHYLCYTOSINE; MUTATION; N6-METHYLADENOSINE; METHYLTRANSFERASE; PSEUDOURIDYLATION;
D O I
10.1093/bioinformatics/btaa155
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: RNA modifications play critical roles in a series of cellular and developmental processes. Knowledge about the distributions of RNA modifications in the transcriptomes will provide clues to revealing their functions. Since experimental methods are time consuming and laborious for detecting RNA modifications, computational methods have been proposed for this aim in the past five years. However, there are some drawbacks for both experimental and computational methods in simultaneously identifying modifications occurred on different nucleotides. Results: To address such a challenge, in this article, we developed a new predictor called iMRM, which is able to simultaneously identify m(6)A, m(5)C, m(1)A, psi and A-to-I modifications in Homo sapiens, Mus musculus and Saccharomyces cerevisiae. In iMRM, the feature selection technique was used to pick out the optimal features. The results from both 10-fold cross-validation and jackknife test demonstrated that the performance of iMRM is superior to existing methods for identifying RNA modifications.
引用
收藏
页码:3336 / 3342
页数:7
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