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DISCOVERY OF FUNCTIONAL AND DISEASE PATHWAYS BY COMMUNITY DETECTION IN PROTEIN-PROTEIN INTERACTION NETWORKS

机译:群体蛋白质互动网络中群落检测发现功能和疾病途径

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Advances in cellular, molecular, and disease biology depend on the comprehensive characterization of gene interactions and pathways. Traditionally, these pathways are curated manually, limiting their efficient annotation and, potentially, reinforcing field-specific bias. Here, in order to test objective and automated identification of functionally cooperative genes, we compared a novel algorithm with three established methods to search for communities within gene interaction networks. Communities identified by the novel approach and by one of the established method overlapped significantly(q < 0.1)with control pathways. With respect to disease, these communities were biased to genes with pathogenic variants in ClinVar(p < 0.01), and often genes from the same community were co-expressed, including in breast cancers. The interesting subset of novel communities, defined by poor overlap to control pathways also contained co-expressed genes, consistent with a possible functional role. This work shows that community detection based on topological features of networks suggests new, biologically meaningful groupings of genes that, in turn, point to health and disease relevant hypotheses.
机译:细胞,分子和疾病生物学的进步取决于基因相互作用和途径的综合表征。传统上,这些途径是手动策划,限制了它们的有效注释,并且可能加强现场特异性偏差。这里,为了测试目的和自动识别功能合作基因,我们将一种新的算法与三种建立的方法进行了比较,以搜索基因交互网络中的社区。由新型方法识别的社区,并通过具有控制途径的明显重叠(Q <0.1)重叠的群落。关于疾病,这些群体偏向于临床中的病原变体(P <0.01),并且来自同一社区的通常是共同表达的,包括乳腺癌。通过不良重叠对控制途径定义的有趣的新界子集还含有与可能的功能作用一致的共表达基因。这项工作表明,基于网络拓扑特征的社区检测表明,新的生物有意义的基因分组,反过来指向健康和疾病相关假设。

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