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Protein complex detection with semi-supervised learning in protein interaction networks

机译:蛋白质相互作用网络中半监督学习的蛋白质复合物检测

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Background Protein-protein interactions (PPIs) play fundamental roles in nearly all biological processes. The systematic analysis of PPI networks can enable a great understanding of cellular organization, processes and function. In this paper, we investigate the problem of protein complex detection from noisy protein interaction data, i.e., finding the subsets of proteins that are closely coupled via protein interactions. However, protein complexes are likely to overlap and the interaction data are very noisy. It is a great challenge to effectively analyze the massive data for biologically meaningful protein complex detection. Results Many people try to solve the problem by using the traditional unsupervised graph clustering methods. Here, we stand from a different point of view, redefining the properties and features for protein complexes and designing a “semi-supervised” method to analyze the problem. In this paper, we utilize the neural network with the “semi-supervised” mechanism to detect the protein complexes. By retraining the neural network model recursively, we could find the optimized parameters for the model, in such a way we can successfully detect the protein complexes. The comparison results show that our algorithm could identify protein complexes that are missed by other methods. We also have shown that our method achieve better precision and recall rates for the identified protein complexes than other existing methods. In addition, the framework we proposed is easy to be extended in the future. Conclusions Using a weighted network to represent the protein interaction network is more appropriate than using a traditional unweighted network. In addition, integrating biological features and topological features to represent protein complexes is more meaningful than using dense subgraphs. Last, the “semi-supervised” learning model is a promising model to detect protein complexes with more biological and topological features available.
机译:背景技术蛋白质-蛋白质相互作用(PPI)在几乎所有生物过程中都起着基本作用。对PPI网络的系统分析可以使人们对蜂窝组织,过程和功能有很好的了解。在本文中,我们研究了从嘈杂的蛋白质相互作用数据中检测蛋白质复合物的问题,即找到通过蛋白质相互作用紧密耦合的蛋白质子集。但是,蛋白质复合物可能会重叠,并且相互作用数据非常嘈杂。有效地分析大量数据以进行生物学上有意义的蛋白质复合物检测是一个巨大的挑战。结果许多人试图通过使用传统的无监督图聚类方法来解决该问题。在这里,我们从不同的角度出发,重新定义了蛋白质复合物的特性和特征,并设计了一种“半监督”方法来分析问题。在本文中,我们利用具有“半监督”机制的神经网络来检测蛋白质复合物。通过递归地训练神经网络模型,我们可以找到模型的优化参数,从而可以成功地检测蛋白质复合物。比较结果表明,我们的算法可以识别其他方法遗漏的蛋白质复合物。我们还表明,与其他现有方法相比,我们的方法对已鉴定的蛋白质复合物具有更高的精度和召回率。此外,我们提出的框架将来很容易扩展。结论使用加权网络表示蛋白质相互作用网络比使用传统的非加权网络更合适。此外,整合生物学特征和拓扑特征以表示蛋白质复合物比使用密集子图更有意义。最后,“半监督”学习模型是一种有前途的模型,可以检测具有更多生物学和拓扑学特征的蛋白质复合物。

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