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Multivariate Information Fusion With Fast Kernel Learning to Kernel Ridge Regression in Predicting LncRNA-Protein Interactions

机译:多元信息融合与快速核学习对预测LncRNA-蛋白质相互作用的核岭回归。

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摘要

Long non-coding RNAs (lncRNAs) constitute a large class of transcribed RNA molecules. They have a characteristic length of more than 200 nucleotides which do not encode proteins. They play an important role in regulating gene expression by interacting with the homologous RNA-binding proteins. Due to the laborious and time-consuming nature of wet experimental methods, more researchers should pay great attention to computational approaches for the prediction of lncRNA-protein interaction (LPI). An in-depth literature review in the state-of-the-art in silico investigations, leads to the conclusion that there is still room for improving the accuracy and velocity. This paper propose a novel method for identifying LPI by employing Kernel Ridge Regression, based on Fast Kernel Learning (LPI-FKLKRR). This approach, uses four distinct similarity measures for lncRNA and protein space, respectively. It is remarkable, that we extract Gene Ontology (GO) with proteins, in order to improve the quality of information in protein space. The process of heterogeneous kernels integration, applies Fast Kernel Learning (FastKL) to deal with weight optimization. The extrapolation model is obtained by gaining the ultimate prediction associations, after using Kernel Ridge Regression (KRR). Experimental outcomes show that the ability of modeling with LPI-FKLKRR has extraordinary performance compared with LPI prediction schemes. On benchmark dataset, it has been observed that the best Area Under Precision Recall Curve (AUPR) of 0.6950 is obtained by our proposed model LPI-FKLKRR, which outperforms the integrated LPLNP (AUPR: 0.4584), RWR (AUPR: 0.2827), CF (AUPR: 0.2357), LPIHN (AUPR: 0.2299), and LPBNI (AUPR: 0.3302). Also, combined with the experimental results of a case study on a novel dataset, it is anticipated that LPI-FKLKRR will be a useful tool for LPI prediction.
机译:长的非编码RNA(lncRNA)构成了一类转录的RNA分子。它们的特征长度超过200个不编码蛋白质的核苷酸。它们通过与同源RNA结合蛋白相互作用,在调节基因表达中起重要作用。由于湿法实验方法耗时费力,因此更多的研究人员应高度重视预测lncRNA-蛋白质相互作用(LPI)的计算方法。在最新的计算机模拟研究中,深入的文献综述得出结论,仍然存在提高准确性和速度的空间。本文提出了一种基于快速核学习(LPI-FKLKRR)的利用核岭回归来识别LPI的新方法。该方法分别对lncRNA和蛋白质空间使用四个不同的相似性度量。值得注意的是,我们从蛋白质中提取基因本体论(GO),以提高蛋白质空间中的信息质量。异构内核集成的过程应用快速内核学习(FastKL)来处理权重优化。在使用内核岭回归(KRR)之后,通过获得最终预测关联来获得外推模型。实验结果表明,与LPI预测方案相比,使用LPI-FKLKRR建模的能力具有非凡的性能。在基准数据集上,已经观察到,我们提出的模型LPI-FKLKRR获得了0.6950的最佳精确召回曲线面积(AUPR),该模型优于集成的LPLNP(AUPR:0.4584),RWR(AUPR:0.2827),CF (AUPR:0.2357),LPIHN(AUPR:0.2299)和LPBNI(AUPR:0.3302)。此外,结合对新型数据集进行案例研究的实验结果,可以预期LPI-FKLKRR将成为LPI预测的有用工具。

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