An ensemble deep learning framework for multi-class LncRNA subcellular localization with innovative encoding strategy.

IF 4.5 1区 生物学 Q1 BIOLOGY BMC Biology Pub Date : 2025-02-21 DOI:10.1186/s12915-025-02148-4
Wenxing Hu, Yan Yue, Ruomei Yan, Lixin Guan, Mengshan Li
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Abstract

Background: Long non-coding RNA (LncRNA) play pivotal roles in various cellular processes, and elucidating their subcellular localization can offer crucial insights into their functional significance. Accurate prediction of lncRNA subcellular localization is of paramount importance. Despite numerous computational methods developed for this purpose, existing approaches still encounter challenges stemming from the complexity of data representation and the difficulty in capturing nucleotide distribution information within sequences.

Results: In this study, we propose a novel deep learning-based model, termed MGBLncLoc, which incorporates a unique multi-class encoding technique known as generalized encoding based on the Distribution Density of Multi-Class Nucleotide Groups (MCD-ND). This encoding approach enables more precise reflection of nucleotide distributions, distinguishing between constant and discriminative regions within sequences, thereby enhancing prediction performance. Additionally, our deep learning model integrates advanced neural network modules, including Multi-Dconv Head Transposed Attention, Gated-Dconv Feed-forward Network, Convolutional Neural Network, and Bidirectional Gated Recurrent Unit, to comprehensively exploit sequence features of lncRNA.

Conclusions: Comparative analysis against commonly used sequence feature encoding methods and existing prediction models validates the effectiveness of MGBLncLoc, demonstrating superior performance. This research offers novel insights and effective solutions for predicting lncRNA subcellular localization, thereby providing valuable support for related biological investigations.

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基于创新编码策略的多类LncRNA亚细胞定位集成深度学习框架。
背景:长链非编码RNA (LncRNA)在各种细胞过程中发挥着关键作用,阐明其亚细胞定位可以为了解其功能意义提供重要见解。准确预测lncRNA亚细胞定位至关重要。尽管为此目的开发了许多计算方法,但现有方法仍然遇到来自数据表示复杂性和难以捕获序列内核苷酸分布信息的挑战。结果:在这项研究中,我们提出了一种新的基于深度学习的模型,称为MGBLncLoc,它结合了一种独特的多类编码技术,即基于多类核苷酸群分布密度的广义编码(MCD-ND)。这种编码方法能够更精确地反映核苷酸分布,区分序列内的恒定区和判别区,从而提高预测性能。此外,我们的深度学习模型集成了先进的神经网络模块,包括Multi-Dconv头部转置注意、门控- dconv前馈网络、卷积神经网络和双向门控循环单元,以全面利用lncRNA的序列特征。结论:通过与常用序列特征编码方法和现有预测模型的对比分析,验证了MGBLncLoc算法的有效性,显示出优越的性能。本研究为预测lncRNA亚细胞定位提供了新颖的见解和有效的解决方案,从而为相关的生物学研究提供了有价值的支持。
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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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