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Exploring local discriminative information from evolutionary profiles for cytokine receptor interaction prediction

机译:从进化谱中探索局部判别信息,以预测细胞因子受体的相互作用

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摘要

Cytokine-receptor interaction is one of the most important types of protein-protein interactions that are widely involved in cellular regulatory processes. Knowledge of cytokine-receptor interactions facilitates to deeply understand several physiological functions. In post-genomic era of sequence explosion, there is an increasing demand for developing machine learning based computational methods for the fast and accurate cytokine-receptor interaction prediction. However, the major problem lying on existing machine learning based methods is that the overall prediction accuracy is relatively low. To improve the accuracy, a crucial step is to establish a well-defined feature representation algorithm. Motivated on this perspective, we propose a novel feature representation method by integrating local information embedded in evolutionary profiles with the Pse-PSSM and AAC-PSSM-AC feature models. We further develop an improved prediction method, namely CRI-Pred, based on the proposed feature set using the Random Forest classifier. Experimental results evaluated with the jackknife test show that the CRI-Pred predictor outperforms the state-of-the-art methods, 5.1% higher in terms of the overall accuracy. This indicates the effectiveness and superiority of CRI-Pred. A webserver that implements CRI-Pred is now freely available at http://server.malab.cn/CRIPred/Index.html to the public to use in practical applications. (C) 2016 Elsevier B.V. All rights reserved.
机译:细胞因子-受体相互作用是广泛参与细胞调节过程的最重要的蛋白-蛋白相互作用类型之一。细胞因子-受体相互作用的知识有助于深入了解几种生理功能。在后序列爆炸的基因组时代,对基于机器学习的计算方法进行快速准确的细胞因子-受体相互作用预测的需求日益增长。但是,现有的基于机器学习的方法存在的主要问题是总体预测精度相对较低。为了提高准确性,关键的一步是建立定义良好的特征表示算法。基于这种观点,我们提出了一种新颖的特征表示方法,该方法通过将嵌入在进化轮廓中的局部信息与Pse-PSSM和AAC-PSSM-AC特征模型相集成来提出。我们基于使用随机森林分类器的特征集,进一步开发了一种改进的预测方法,即CRI-Pred。用折刀试验评估的实验结果表明,CRI-Pred预测器的性能优于最新方法,总体精度高5.1%。这表明了CRI-Pred的有效性和优越性。现在可以在http://server.malab.cn/CRIPred/Index.html上免费获得实现CRI-Pred的Web服务器,以供公众在实际应用中使用。 (C)2016 Elsevier B.V.保留所有权利。

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