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Improving protein–protein interactions prediction accuracy using protein evolutionary information and relevance vector machine model

机译:使用蛋白质进化信息和相关向量机模型提高蛋白质间相互作用的预测准确性

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摘要

Predicting protein–protein interactions (PPIs) is a challenging task and essential to construct the protein interaction networks, which is important for facilitating our understanding of the mechanisms of biological systems. Although a number of high‐throughput technologies have been proposed to predict PPIs, there are unavoidable shortcomings, including high cost, time intensity, and inherently high false positive rates. For these reasons, many computational methods have been proposed for predicting PPIs. However, the problem is still far from being solved. In this article, we propose a novel computational method called RVM‐BiGP that combines the relevance vector machine (RVM) model and Bi‐gram Probabilities (BiGP) for PPIs detection from protein sequences. The major improvement includes (1) Protein sequences are represented using the Bi‐gram probabilities (BiGP) feature representation on a Position Specific Scoring Matrix (PSSM), in which the protein evolutionary information is contained; (2) For reducing the influence of noise, the Principal Component Analysis (PCA) method is used to reduce the dimension of BiGP vector; (3) The powerful and robust Relevance Vector Machine (RVM) algorithm is used for classification. Five‐fold cross‐validation experiments executed on yeast and Helicobacter pylori datasets, which achieved very high accuracies of 94.57 and 90.57%, respectively. Experimental results are significantly better than previous methods. To further evaluate the proposed method, we compare it with the state‐of‐the‐art support vector machine (SVM) classifier on the yeast dataset. The experimental results demonstrate that our RVM‐BiGP method is significantly better than the SVM‐based method. In addition, we achieved 97.15% accuracy on imbalance yeast dataset, which is higher than that of balance yeast dataset. The promising experimental results show the efficiency and robust of the proposed method, which can be an automatic decision support tool for future proteomics research. For facilitating extensive studies for future proteomics research, we developed a freely available web server called RVM‐BiGP‐PPIs in Hypertext Preprocessor (PHP) for predicting PPIs. The web server including source code and the datasets are available at .
机译:预测蛋白质间相互作用(PPI)是一项艰巨的任务,对于构建蛋白质相互作用网络至关重要,这对于促进我们对生物系统机理的理解至关重要。尽管已提出了许多高通量技术来预测PPI,但仍存在不可避免的缺点,包括成本高,时间强度大和固有的假阳性率高。由于这些原因,已经提出了许多用于预测PPI的计算方法。但是,这个问题仍然远远没有解决。在本文中,我们提出了一种称为RVM-BiGP的新颖计算方法,该方法结合了相关向量机(RVM)模型和Bi-gram概率(BiGP)从蛋白质序列中检测PPI。主要的改进包括:(1)使用Bigram概率(BiGP)特征表示法在特定位置评分矩阵(PSSM)上表示蛋白质序列,其中包含蛋白质进化信息; (2)为了减少噪声的影响,使用主成分分析(PCA)方法来减小BiGP向量的维数; (3)强大而健壮的关联向量机(RVM)算法用于分类。在酵母和幽门螺杆菌数据集上进行了五次交叉验证实验,分别达到了94.57和90.57%的极高准确度。实验结果明显优于以前的方法。为了进一步评估提出的方法,我们将其与酵母数据集上的最新支持向量机(SVM)分类器进行了比较。实验结果表明,我们的RVM-BiGP方法明显优于基于SVM的方法。此外,我们在不平衡酵母数据集上达到了97.15%的准确度,高于平衡酵母数据集的准确度。有希望的实验结果证明了该方法的有效性和鲁棒性,可以作为未来蛋白质组学研究的自动决策支持工具。为了便于对将来的蛋白质组学研究进行广泛的研究,我们开发了可免费使用的Web服务器,称为超文本预处理器(PHP)中的RVM-BiGP-PPI,用于预测PPI。包含源代码和数据集的Web服务器位于。

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