SVM-LncRNAPro: An SVM-Based Method for Predicting Long Noncoding RNA Promoters

IF 1.9 4区 生物学 Q4 CELL BIOLOGY IET Systems Biology Pub Date : 2025-04-05 DOI:10.1049/syb2.70013
Guohua Huang, Taigan Xue, Weihong Chen, Liangliang Huang, Qi Dai, JinYun Jiang
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Abstract

Long non-coding RNAs (lncRNAs) are closely associated with the regulation of gene expression, whose promoters play a crucial role in comprehensively understanding lncRNA regulatory mechanisms, functions and their roles in diseases. Due to limitations of the current techniques, accurately identifying lncRNA promoters remains a challenge. To address this challenge, we propose a support vector machine (SVM)–based method for predicting lncRNA promoters, called SVM-LncRNAPro. This method uses position-specific trinucleotide propensity based on single-strand (PSTNPss) to encode the DNA sequences and employs an SVM as the learning algorithm. The SVM-LncRNAPro achieves state-of-the-art performance with reduced complexity. Additionally, experiments demonstrate that this method exhibits a strong generalisation ability. For the convenience of academic research, we have made the source code of SVM-LncRNAPro publicly available. Researchers can download the code and perform the prediction of the lncRNA promoter via the following link: https://github.com/TG0F7/Prom/tree/master.

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基于支持向量机的长链非编码RNA启动子预测方法
长链非编码rna (Long non-coding RNAs, lncRNAs)与基因表达调控密切相关,其启动子对于全面了解lncRNA调控机制、功能及其在疾病中的作用起着至关重要的作用。由于当前技术的局限性,准确识别lncRNA启动子仍然是一个挑战。为了解决这一挑战,我们提出了一种基于支持向量机(SVM)的预测lncRNA启动子的方法,称为SVM- lncrnapro。该方法采用基于单链的位置特异性三核苷酸倾向(PSTNPss)对DNA序列进行编码,并采用支持向量机作为学习算法。SVM-LncRNAPro在降低复杂性的同时实现了最先进的性能。实验表明,该方法具有较强的泛化能力。为了方便学术研究,我们公开了SVM-LncRNAPro的源代码。研究人员可以通过以下链接下载代码并对lncRNA启动子进行预测:https://github.com/TG0F7/Prom/tree/master。
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来源期刊
IET Systems Biology
IET Systems Biology 生物-数学与计算生物学
CiteScore
4.20
自引率
4.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: IET Systems Biology covers intra- and inter-cellular dynamics, using systems- and signal-oriented approaches. Papers that analyse genomic data in order to identify variables and basic relationships between them are considered if the results provide a basis for mathematical modelling and simulation of cellular dynamics. Manuscripts on molecular and cell biological studies are encouraged if the aim is a systems approach to dynamic interactions within and between cells. The scope includes the following topics: Genomics, transcriptomics, proteomics, metabolomics, cells, tissue and the physiome; molecular and cellular interaction, gene, cell and protein function; networks and pathways; metabolism and cell signalling; dynamics, regulation and control; systems, signals, and information; experimental data analysis; mathematical modelling, simulation and theoretical analysis; biological modelling, simulation, prediction and control; methodologies, databases, tools and algorithms for modelling and simulation; modelling, analysis and control of biological networks; synthetic biology and bioengineering based on systems biology.
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