MultiV_Nm:一种基于多视图特征的2'- o -甲基化位点预测方法。

IF 2.8 3区 生物学 Q2 GENETICS & HEREDITY
Frontiers in Genetics Pub Date : 2025-05-27 eCollection Date: 2025-01-01 DOI:10.3389/fgene.2025.1608490
Lei Bai, Fei Liu, Yile Wang, Junle Su, Lian Liu
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引用次数: 0

摘要

2'- o -甲基化修饰(2'-O-methylation modification,简称Nm)是一类重要的化学修饰,广泛存在于各种生物体中,在细胞正常生理活动和疾病的发生发展中起着非常重要的作用。准确预测纳米修饰位点可以为疾病的诊断和治疗以及潜在药物靶点的鉴定提供重要参考。针对目前使用单一特征导致性能不稳定的问题,以及提高纳米修饰位点预测精度的需要,本文提出了基于多视图特征的纳米位点预测方法MultiV_Nm。MultiV_Nm从多个维度提取Nm位点的特征,包括序列特征、化学特征和二级结构特征。通过融合卷积神经网络强大的局部特征提取能力、图注意网络捕获全局结构信息的能力以及不同特征的交叉注意机制的高效交互优势,对多视图特征进行深度挖掘和融合,最终实现Nm修饰位点的预测。交叉验证和独立测试结果表明,该方法在精密度、召回率和准确度等关键评价指标上具有显著优势,能够有效提高纳米位点的预测性能。MultiV_Nm的提出不仅为纳米修饰的研究提供了有力的工具,也为预测其他RNA修饰位点提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MultiV_Nm: a prediction method for 2'-O-methylation sites based on multi-view features.

As a crucial class of chemical modifications, 2'-O-methylation modification (abbreviated as Nm) is widely distributed in various organisms and plays a very important role in normal cellular physiological activities and the occurrence and development of diseases. Accurate prediction of Nm modification sites can provide important references for the diagnosis and treatment of diseases, as well as identifying for potential drug targets. Aiming at the current problems of unstable performance caused by the use of single features and the need to improve the prediction accuracy of Nm modification sites, this paper proposes MultiV_Nm, a prediction method for Nm sites based on multi-view features. MultiV_Nm extracts the features of Nm sites from multiple dimensions, including sequence features, chemical characteristics, and secondary structure features. By integrating the powerful local feature extraction ability of convolutional neural networks, the ability of graph attention networks to capture global structural information, and the efficient interaction advantage of cross-attention mechanisms for different features, it deeply explores and integrates multi-view features, and finally realizes the prediction of Nm modification sites. The results of cross-validation and independent tests show that this method exhibits significant advantages in key evaluation indicators such as precision, recall, and accuracy, and can effectively improve Nm sites prediction performance. The proposal of MultiV_Nm not only provides a powerful tool for the study of Nm modification but also offers new ideas for predicting other RNA modification sites.

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来源期刊
Frontiers in Genetics
Frontiers in Genetics Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
5.50
自引率
8.10%
发文量
3491
审稿时长
14 weeks
期刊介绍: Frontiers in Genetics publishes rigorously peer-reviewed research on genes and genomes relating to all the domains of life, from humans to plants to livestock and other model organisms. Led by an outstanding Editorial Board of the world’s leading experts, this multidisciplinary, open-access journal is at the forefront of communicating cutting-edge research to researchers, academics, clinicians, policy makers and the public. The study of inheritance and the impact of the genome on various biological processes is well documented. However, the majority of discoveries are still to come. A new era is seeing major developments in the function and variability of the genome, the use of genetic and genomic tools and the analysis of the genetic basis of various biological phenomena.
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