iR6mA-RNN: Identifying N6-Methyladenosine Sites in Eukaryotic Transcriptomes using Recurrent Neural Networks and Sequence-embedded Features

Binh P. Nguyen, T. Nguyen-Vo, Loc Nguyen, Quang H. Trinh, Chalinor Baliuag, T. Do, S. Rahardja
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Abstract

As a common biological event observed in all living creatures, RNA modification is an essential post-transcriptional factor that regulates the activity, localization, and stability of RNAs. Multiple diseases are associated with RNA modification. N6-methyladenosine (6mA) modification of RNA is one of the most frequent events that affect the translational processes and structural stability of modified transcripts and control transcriptional processes in cell state maintenance and transition. To detect 6mA sites in eukaryotic transcriptomes, a number of computational models were developed as online applications to assist experimental scientists in reducing human effort and budget. However, most of those online web servers are now either outdated or inaccessible. In this study, we propose iR6mA-RNN, an effective computational framework using recurrent neural networks and sequence-embedded features, to predict possible 6mA sites in eukaryotic transcriptomes. When tested on an independent test set, the proposed model achieved an area under the receiver operating characteristic curve of 0.7972 and an area under the precision-recall curve of 0.7785. Our model also outperformed the other two existing methods. Results from another sensitivity analysis confirmed the stability of the model as well.
iR6mA-RNN:利用递归神经网络和序列嵌入特征识别真核生物转录组中的n6 -甲基腺苷位点
RNA修饰是所有生物普遍存在的生物学事件,是调控RNA活性、定位和稳定性的重要转录后因子。多种疾病与RNA修饰有关。n6 -甲基腺苷(n6 - methylladenosine, 6mA)修饰RNA是影响修饰后转录物的翻译过程和结构稳定性,控制细胞状态维持和转变的转录过程的最常见事件之一。为了检测真核生物转录组中的6mA位点,许多计算模型被开发为在线应用程序,以帮助实验科学家减少人力和预算。然而,大多数在线网络服务器现在要么过时,要么无法访问。在这项研究中,我们提出了iR6mA-RNN,这是一个有效的计算框架,使用循环神经网络和序列嵌入特征来预测真核生物转录组中可能的6mA位点。在独立测试集上进行测试时,该模型在接收者工作特征曲线下的面积为0.7972,在精确召回率曲线下的面积为0.7785。我们的模型也优于其他两种现有的方法。另一项敏感性分析的结果也证实了模型的稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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