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LPI-IBNRA: Long Non-coding RNA-Protein Interaction Prediction Based on Improved Bipartite Network Recommender Algorithm

机译:LPI-IBNRA:基于改进的双向网络推荐算法的长时间非编码RNA-蛋白质相互作用预测

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摘要

According to the latest research, lncRNAs (long non-coding RNAs) play a broad and important role in various biological processes by interacting with proteins. However, identifying whether proteins interact with a specific lncRNA through biological experimental methods is difficult, costly, and time-consuming. Thus, many bioinformatics computational methods have been proposed to predict lncRNA-protein interactions. In this paper, we proposed a novel approach called Long non-coding RNA-Protein Interaction Prediction based on Improved Bipartite Network Recommender Algorithm (LPI-IBNRA). In the proposed method, we implemented a two-round resource allocation and eliminated the second-order correlations appropriately on the bipartite network. Experimental results illustrate that LPI-IBNRA outperforms five previous methods, with the AUC values of 0.8932 in leave-one-out cross validation (LOOCV) and 0.8819 ± 0.0052 in 10-fold cross validation, respectively. In addition, case studies on four lncRNAs were carried out to show the predictive power of LPI-IBNRA.
机译:根据最新研究,lncRNA(长非编码RNA)通过与蛋白质相互作用,在各种生物过程中发挥着广泛而重要的作用。但是,通过生物学实验方法鉴定蛋白质是否与特定的lncRNA相互作用是困难,昂贵和费时的。因此,已经提出了许多生物信息学计算方法来预测lncRNA-蛋白质相互作用。在本文中,我们提出了一种基于改进的双向网络推荐算法(LPI-IBNRA)的新方法,称为长非编码RNA-蛋白质相互作用预测。在提出的方法中,我们实现了两轮资源分配,并在二分网络上适当地消除了二阶相关性。实验结果表明,LPI-IBNRA优于之前的五种方法,留一法交叉验证(LOOCV)的AUC值为0.8932,而十倍交叉验证的AUC值为0.8819±0.0052。此外,对四个lncRNA进行了案例研究,以显示LPI-IBNRA的预测能力。

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