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A network-based pathway-expanding approach for pathway analysis

机译:基于网络的路径扩展方法进行路径分析

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Background Pathway analysis combining multiple types of high-throughput data, such as genomics and proteomics, has become the first choice to gain insights into the pathogenesis of complex diseases. Currently, several pathway analysis methods have been developed to study complex diseases. However, these methods did not take into account the interaction between internal and external genes of the pathway and between pathways. Hence, these approaches still face some challenges. Here, we propose a network-based pathway-expanding approach that takes the topological structures of biological networks into account. Results First, two weighted gene-gene interaction networks (tumor and normal) are constructed integrating protein-protein interaction(PPI) information, gene expression data and pathway databases. Then, they are used to identify significant pathways through testing the difference of topological structures of expanded pathways in the two weighted networks. The proposed method is employed to analyze two breast cancer data. As a result, the top 15 pathways identified using the proposed method are supported by biological knowledge from the published literatures and other methods. In addition, the proposed method is also compared with other methods, such as GSEA and SPIA, and estimated using the classification performance of the top 15 expanded pathways. Conclusions A novel network-based pathway-expanding approach is proposed to avoid the limitations of existing pathway analysis approaches. Experimental results indicate that the proposed method can accurately and reliably identify significant pathways which are related to the corresponding disease.
机译:背景途径分析结合了多种类型的高通量数据,例如基因组学和蛋白质组学,已成为了解复杂疾病发病机理的首选方法。当前,已经开发了几种途径分析方法来研究复杂疾病。但是,这些方法没有考虑途径的内部和外部基因之间以及途径之间的相互作用。因此,这些方法仍然面临一些挑战。在这里,我们提出了一种基于网络的路径扩展方法,该方法考虑了生物网络的拓扑结构。结果首先,结合蛋白质-蛋白质相互作用(PPI)信息,基因表达数据和途径数据库,构建了两个加权的基因-基因相互作用网络(肿瘤和正常)。然后,通过测试两个加权网络中扩展路径的拓扑结构差异,将它们用于识别重要路径。所提出的方法用于分析两个乳腺癌数据。结果,使用所提出的方法确定的前15条途径得到了已发表文献和其他方法的生物学知识的支持。此外,还将所提出的方法与其他方法(例如GSEA和SPIA)进行比较,并使用前15条扩展途径的分类性能进行估算。结论提出了一种新颖的基于网络的途径扩展方法,以避免现有途径分析方法的局限性。实验结果表明,该方法可以准确,可靠地确定与相应疾病有关的重要途径。

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