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Prediction of Cancer Proteins by Integrating Protein Interaction, Domain Frequency, and Domain Interaction Data Using Machine Learning Algorithms

机译:通过使用机器学习算法整合蛋白质相互作用,域频率和域相互作用数据来预测癌症蛋白

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Many proteins are known to be associated with cancer diseases. It is quite often that their precise functional role in disease pathogenesis remains unclear. A strategy to gain a better understanding of the function of these proteins is to make use of a combination of different aspects of proteomics data types. In this study, we extended Aragues’s method by employing the protein-protein interaction (PPI) data, domain-domain interaction (DDI) data, weighted domain frequency score (DFS), and cancer linker degree (CLD) data to predict cancer proteins. Performances were benchmarked based on three kinds of experiments as follows: (I) using individual algorithm, (II) combining algorithms, and (III) combining the same classification types of algorithms. When compared with Aragues’s method, our proposed methods, that is, machine learning algorithm and voting with the majority, are significantly superior in all seven performance measures. We demonstrated the accuracy of the proposed method on two independent datasets. The best algorithm can achieve a hit ratio of 89.4% and 72.8% for lung cancer dataset and lung cancer microarray study, respectively. It is anticipated that the current research could help understand disease mechanisms and diagnosis.
机译:已知许多蛋白质与癌症疾病有关。尚不清楚它们在疾病发病机理中的确切功能作用。更好地了解这些蛋白质功能的策略是利用蛋白质组学数据类型不同方面的组合。在这项研究中,我们通过使用蛋白质-蛋白质相互作用(PPI)数据,域-域相互作用(DDI)数据,加权域频率得分(DFS)和癌症接头程度(CLD)数据来扩展Aragues方法来预测癌症蛋白。基于以下三种实验对性能进行基准测试:(I)使用单个算法,(II)组合算法,(III)组合相同分类类型的算法。与Aragues的方法相比,我们提出的方法(即机器学习算法和多数表决)在所有七个性能指标上均明显优于其他方法。我们在两个独立的数据集上证明了该方法的准确性。对于肺癌数据集和肺癌微阵列研究,最佳算法可以分别达到89.4%和72.8%的命中率。可以预期,当前的研究将有助于理解疾病的机制和诊断。

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