MJnet: A lightweight RNN-based model for microRNA target site prediction

IF 3.1 4区 生物学 Q2 BIOLOGY
Junhao Yu, Cong Hui, Jianhua Jia
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引用次数: 0

Abstract

Accurate prediction of microRNA (miRNA) target sites is critical for understanding post-transcriptional gene regulation. While recent deep learning models have achieved high predictive accuracy, many suffer from excessive computational complexity and limited interpretability. In this study, we propose MJnet, a lightweight and efficient deep learning model based on a Bidirectional Gated Recurrent Unit (BiGRU) architecture, integrated with simple C2 encoding, a multi-scale one-dimensional convolutional network (TextCNN), and a self-attention mechanism. This framework captures both local sequence features and global contextual dependencies while maintaining low computational cost. Extensive experiments on experimentally validated datasets demonstrate that our model outperforms several traditional and deep learning-based baselines, including Mimosa, in terms of accuracy, F1-score, and robustness across balanced gene-level test sets. Ablation studies confirm the effectiveness of each module, and attention heatmaps reveal interpretable patterns aligned with known seed regions. Our approach offers a practical, reproducible, and interpretable solution for miRNA target site prediction in biologically relevant contexts.
MJnet:一个轻量级的基于rnn的microRNA靶位预测模型
准确预测microRNA (miRNA)靶位对于理解转录后基因调控至关重要。虽然最近的深度学习模型已经取得了很高的预测准确性,但许多模型都存在计算复杂性过高和可解释性有限的问题。在这项研究中,我们提出了MJnet,一个基于双向门控循环单元(BiGRU)架构的轻量级高效深度学习模型,集成了简单的C2编码、多尺度一维卷积网络(TextCNN)和自注意机制。该框架捕获了局部序列特征和全局上下文依赖关系,同时保持了较低的计算成本。在经过实验验证的数据集上进行的大量实验表明,我们的模型在准确性、f1分数和平衡基因水平测试集的稳健性方面优于几种传统的和基于深度学习的基线,包括含羞草。消融研究证实了每个模块的有效性,注意力热图揭示了与已知种子区域一致的可解释模式。我们的方法为生物学相关背景下的miRNA靶点预测提供了一种实用、可重复和可解释的解决方案。
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来源期刊
Computational Biology and Chemistry
Computational Biology and Chemistry 生物-计算机:跨学科应用
CiteScore
6.10
自引率
3.20%
发文量
142
审稿时长
24 days
期刊介绍: Computational Biology and Chemistry publishes original research papers and review articles in all areas of computational life sciences. High quality research contributions with a major computational component in the areas of nucleic acid and protein sequence research, molecular evolution, molecular genetics (functional genomics and proteomics), theory and practice of either biology-specific or chemical-biology-specific modeling, and structural biology of nucleic acids and proteins are particularly welcome. Exceptionally high quality research work in bioinformatics, systems biology, ecology, computational pharmacology, metabolism, biomedical engineering, epidemiology, and statistical genetics will also be considered. Given their inherent uncertainty, protein modeling and molecular docking studies should be thoroughly validated. In the absence of experimental results for validation, the use of molecular dynamics simulations along with detailed free energy calculations, for example, should be used as complementary techniques to support the major conclusions. Submissions of premature modeling exercises without additional biological insights will not be considered. Review articles will generally be commissioned by the editors and should not be submitted to the journal without explicit invitation. However prospective authors are welcome to send a brief (one to three pages) synopsis, which will be evaluated by the editors.
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