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Combining High Speed ELM Learning with a Deep Convolutional Neural Network Feature Encoding for Predicting Protein-RNA Interactions

机译:将高速榆树学习与深度卷积神经网络特征合并,用于预测蛋白质RNA相互作用的编码

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摘要

Emerging evidence has shown that RNA plays a crucial role in many cellular processes, and their biological functions are primarily achieved by binding with a variety of proteins. High-throughput biological experiments provide a lot of valuable information for the initial identification of RNA-protein interactions (RPIs), but with the increasing complexity of RPIs networks, this method gradually falls into expensive and time-consuming situations. Therefore, there is an urgent need for high speed and reliable methods to predict RNA-protein interactions. In this study, we propose a computational method for predicting the RNA-protein interactions using sequence information. The deep learning convolution neural network (CNN) algorithm is utilized to mine the hidden high-level discriminative features from the RNA and protein sequences and feed it into the extreme learning machine (ELM) classifier. The experimental results with 5-fold cross-validation indicate that the proposed method achieves superior performance on benchmark datasets (RPI1807, RPI2241, and RPI369) with the accuracy of 98.83, 90.83, and 85.63 percent, respectively. We further evaluate the performance of the proposed model by comparing it with the state-of-the-art SVM classifier and other existing methods on the same benchmark data set. In addition, we predicted the independent NPInter v2.0 data set using the model trained on RPI369. The experimental results show that our model can serve as a useful tool for predicting RNA-protein interactions.
机译:出现的证据表明,RNA在许多细胞过程中发挥至关重要的作用,并且它们的生物学功能主要通过与各种蛋白质结合来实现。高通量生物实验为初始鉴定RNA蛋白质相互作用(RPI)提供了许多有价值的信息,但随着RPI网络的复杂性的增加,该方法逐渐落入昂贵且耗时的情况下。因此,迫切需要高速和可靠的方法来预测RNA蛋白质相互作用。在本研究中,我们提出了一种用于使用序列信息预测RNA蛋白质相互作用的计算方法。深度学习卷积神经网络(CNN)算法用于从RNA和蛋白质序列中挖掘隐藏的高级鉴别特征,并将其送入极限学习机(ELM)分类器。具有5倍交叉验证的实验结果表明,该方法在基准数据集(RPI1807,RPI2241和RPI369)上实现了卓越的性能,分别为98.83,90.83和85.63%的准确度。我们通过将其与最先进的SVM分类器和其他现有方法进行比较,进一步评估所提出的模型的性能。此外,我们预测了使用在RPI369上培训的模型进行的独立NPINTER V2.0数据集。实验结果表明,我们的模型可以作为预测RNA蛋白质相互作用的有用工具。

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