| Literature DB >> 27896987 |
Stephen J Wilson1, Angela D Wilkins, Chih-Hsu Lin, Rhonald C Lua, Olivier Lichtarge.
Abstract
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.Entities:
Mesh:
Year: 2017 PMID: 27896987 PMCID: PMC5140035 DOI: 10.1142/9789813207813_0032
Source DB: PubMed Journal: Pac Symp Biocomput ISSN: 2335-6928