iRNA(m6A)-PseDNC: Identifying N6-methyladenosine sites using pseudo dinucleotide composition
- PMID: 30201554
- DOI: 10.1016/j.ab.2018.09.002
iRNA(m6A)-PseDNC: Identifying N6-methyladenosine sites using pseudo dinucleotide composition
Abstract
As a prevalent post-transcriptional modification, N6-methyladenosine (m6A) plays key roles in a series of biological processes. Although experimental technologies have been developed and applied to identify m6A sites, they are still cost-ineffective for transcriptome-wide detections of m6A. As good complements to the experimental techniques, some computational methods have been proposed to identify m6A sites. However, their performance remains unsatisfactory. In this study, we firstly proposed an Euclidean distance based method to construct a high quality benchmark dataset. By encoding the RNA sequences using pseudo nucleotide composition, a new predictor called iRNA(m6A)-PseDNC was developed to identify m6A sites in the Saccharomyces cerevisiae genome. It has been demonstrated by the 10-fold cross validation test that the performance of iRNA(m6A)-PseDNC is superior to the existing methods. Meanwhile, for the convenience of most experimental scientists, established at the site http://lin-group.cn/server/iRNA(m6A)-PseDNC.php is its web-server, by which users can easily get their desired results without need to go through the detailed mathematics. It is anticipated that iRNA(m6A)-PseDNC will become a useful high throughput tool for identifying m6A sites in the S. cerevisiae genome.
Keywords: 5-step rules; N(6)-methyladenosine; Pseudo nucleotide composition; RNA modification; Support vector machine.
Copyright © 2018 Elsevier Inc. All rights reserved.
Similar articles
-
iRNA-Methyl: Identifying N(6)-methyladenosine sites using pseudo nucleotide composition.Anal Biochem. 2015 Dec 1;490:26-33. doi: 10.1016/j.ab.2015.08.021. Epub 2015 Aug 24. Anal Biochem. 2015. PMID: 26314792
-
pRNAm-PC: Predicting N(6)-methyladenosine sites in RNA sequences via physical-chemical properties.Anal Biochem. 2016 Mar 15;497:60-7. doi: 10.1016/j.ab.2015.12.017. Epub 2015 Dec 31. Anal Biochem. 2016. PMID: 26748145
-
Computational identification of N6-methyladenosine sites in multiple tissues of mammals.Comput Struct Biotechnol J. 2020 Apr 30;18:1084-1091. doi: 10.1016/j.csbj.2020.04.015. eCollection 2020. Comput Struct Biotechnol J. 2020. PMID: 32435427 Free PMC article.
-
Comparison and Analysis of Computational Methods for Identifying N6-Methyladenosine Sites in Saccharomyces cerevisiae.Curr Pharm Des. 2021;27(9):1219-1229. doi: 10.2174/1381612826666201109110703. Curr Pharm Des. 2021. PMID: 33167827 Review.
-
Comprehensive review and assessment of computational methods for predicting RNA post-transcriptional modification sites from RNA sequences.Brief Bioinform. 2020 Sep 25;21(5):1676-1696. doi: 10.1093/bib/bbz112. Brief Bioinform. 2020. PMID: 31714956 Review.
Cited by
-
Structural Variability in the RLR-MAVS Pathway and Sensitive Detection of Viral RNAs.Med Chem. 2019;15(5):443-458. doi: 10.2174/1573406415666181219101613. Med Chem. 2019. PMID: 30569868 Free PMC article. Review.
-
Attention-based multi-label neural networks for integrated prediction and interpretation of twelve widely occurring RNA modifications.Nat Commun. 2021 Jun 29;12(1):4011. doi: 10.1038/s41467-021-24313-3. Nat Commun. 2021. PMID: 34188054 Free PMC article.
-
Crosstalk between m6A and coding/non-coding RNA in cancer and detection methods of m6A modification residues.Aging (Albany NY). 2023 Jul 11;15(13):6577-6619. doi: 10.18632/aging.204836. Epub 2023 Jul 11. Aging (Albany NY). 2023. PMID: 37437245 Free PMC article. Review.
-
Interpretable deep cross networks unveiled common signatures of dysregulated epitranscriptomes across 12 cancer types.Mol Ther Nucleic Acids. 2024 Oct 29;35(4):102376. doi: 10.1016/j.omtn.2024.102376. eCollection 2024 Dec 10. Mol Ther Nucleic Acids. 2024. PMID: 39618823 Free PMC article.
-
Neuronal Reg3β/macrophage TNF-α-mediated positive feedback signaling contributes to pain chronicity in a rat model of CRPS-I.Sci Adv. 2025 Aug;11(31):eadu4270. doi: 10.1126/sciadv.adu4270. Epub 2025 Aug 1. Sci Adv. 2025. PMID: 40749060 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials