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RNAMethPre: A Web Server for the Prediction and Query of mRNA m6A Sites
Shunian Xiang1, Ke Liu1,2, Zhangming Yan1
1MOE Key Laboratory of Bioinformatics, School of Life Sciences, Tsinghua University, Beijing, 100084, P. R. China.
Abstract:
N6-Methyladenosine (m6A) is the most common mRNA modification; it occurs in a wide range of taxon and is associated with many key biological processes. High-throughput experiments have identified m6A-peaks and sites across the transcriptome, but studies of m6A sites at the transcriptome-wide scale are limited to a few species and tissue types. Therefore, the computational prediction of mRNA m6A sites has become an important strategy. In this study, we integrated multiple features of mRNA (flanking sequences, local secondary structure information, and relative position information) and trained a SVM classifier to predict m6A sites in mammalian mRNA sequences. Our method achieves ideal performance in both cross-validation tests and rigorous independent dataset tests. The server also provides a comprehensive database of predicted transcriptome-wide m6A sites and curated m6A-seq peaks from the literature for both human and mouse, and these can be queried and visualized in a genome browser. The RNAMethPre web server provides a user-friendly tool for the prediction and query of mRNA m6A sites, which is freely accessible for public use at http://bioinfo.tsinghua.edu.cn/RNAMethPre/index.html.
Insights
N6-Methyladenosine (m6A) is a crucial mRNA modification. This study developed a computational tool to accurately predict m6A sites in mammalian mRNA, aiding further research.
Area of Science:
- Epigenetics and RNA Biology
- Bioinformatics and Computational Biology
Background:
- N6-Methyladenosine (m6A) is the most prevalent mRNA modification, influencing diverse biological processes across many species.
- Transcriptome-wide m6A site identification is limited in scope, necessitating robust computational prediction methods.
Purpose of the Study:
- To develop and validate a computational method for predicting mRNA m6A sites in mammalian sequences.
- To create a user-friendly web server for querying and visualizing predicted and curated m6A sites.
Main Methods:
- Integration of multiple mRNA features: flanking sequences, local secondary structure, and relative position.
- Training a Support Vector Machine (SVM) classifier for m6A site prediction.
- Validation using cross-validation and independent dataset tests.
Main Results:
- The SVM classifier achieved high performance in predicting m6A sites.
- The RNAMethPre web server was established, offering a database of predicted and literature-curated m6A sites for human and mouse.
- The server includes genome browser visualization for queried m6A data.
Conclusions:
- The developed computational method provides an accurate strategy for predicting mRNA m6A sites.
- The RNAMethPre web server serves as a valuable, publicly accessible resource for researchers studying m6A modifications.
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