LPI-ETSLP: lncRNA–protein interaction prediction using eigenvalue transformation-based semi-supervised link prediction

IF 3.743 Q2 Biochemistry, Genetics and Molecular Biology
Huan Hu, Chunyu Zhu, Haixin Ai, Li Zhang, Jian Zhao, Qi Zhao and Hongsheng Liu
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引用次数: 54

Abstract

RNA–protein interactions are essential for understanding many important cellular processes. In particular, lncRNA–protein interactions play important roles in post-transcriptional gene regulation, such as splicing, translation, signaling and even the progression of complex diseases. However, the experimental validation of lncRNA–protein interactions remains time-consuming and expensive, and only a few theoretical approaches are available for predicting potential lncRNA–protein associations. Here, we presented eigenvalue transformation-based semi-supervised link prediction (LPI-ETSLP) to uncover the relationship between lncRNAs and proteins. Moreover, it is semi-supervised and does not need negative samples. Based on 5-fold cross validation, an AUC of 0.8876 and an AUPR of 0.6438 have demonstrated its reliable performance compared with three other computational models. Furthermore, the case study demonstrated that many lncRNA–protein interactions predicted by our method can be successfully confirmed by experiments. It is indicated that LPI-ETSLP would be a useful bioinformatics resource for biomedical research studies.

Abstract Image

LPI-ETSLP:基于特征值变换的lncrna -蛋白相互作用半监督链接预测
rna -蛋白相互作用对于理解许多重要的细胞过程是必不可少的。特别是lncrna -蛋白相互作用在转录后基因调控中发挥重要作用,如剪接、翻译、信号传导甚至复杂疾病的进展。然而,lncrna -蛋白相互作用的实验验证仍然耗时且昂贵,并且只有少数理论方法可用于预测潜在的lncrna -蛋白关联。在这里,我们提出了基于特征值变换的半监督链接预测(LPI-ETSLP)来揭示lncrna和蛋白质之间的关系。此外,它是半监督的,不需要负样本。基于5重交叉验证,AUC为0.8876,AUPR为0.6438,与其他3种计算模型相比,该模型具有可靠的性能。此外,案例研究表明,我们的方法预测的许多lncrna -蛋白相互作用可以通过实验成功证实。指出LPI-ETSLP将成为生物医学研究的一个有用的生物信息学资源。
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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来源期刊
Molecular BioSystems
Molecular BioSystems 生物-生化与分子生物学
CiteScore
2.94
自引率
0.00%
发文量
0
审稿时长
2.6 months
期刊介绍: Molecular Omics publishes molecular level experimental and bioinformatics research in the -omics sciences, including genomics, proteomics, transcriptomics and metabolomics. We will also welcome multidisciplinary papers presenting studies combining different types of omics, or the interface of omics and other fields such as systems biology or chemical biology.
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