Chen Lin, Mukerjee Gouri, Dorfman Ruslan, Moghadas Seyed M
Agent-Based Modelling Laboratory, York University Toronto, ON, Canada.
GeneYouIn Inc. Maple, ON, Canada.
Front Genet. 2017 Mar 7;8:29. doi: 10.3389/fgene.2017.00029. eCollection 2017.
Much effort has been devoted to assess disease risk based on large-scale protein-protein network and genotype-phenotype associations. However, the challenge of risk prediction for complex diseases remains unaddressed. Here, we propose a framework to quantify the risk based on a Voronoi tessellation network analysis, taking into account the disease association scores of both genes and variants. By integrating ClinVar, SNPnexus, and DISEASES databases, we introduce a gene-variant map that is based on the pairwise disease-associated gene-variant scores. This map is clustered using Voronoi tessellation and network analysis with a threshold obtained from fitting the background Voronoi cell density distribution. We define the relative risk of disease that is inferred from the scores of the data points within the related clusters on the gene-variant map. We identify autoimmune-associated clusters that may interact at the system-level. The proposed framework can be used to determine the clusters that are specific to a subtype or contribute to multiple subtypes of complex diseases.
人们已经付出了很多努力,基于大规模蛋白质-蛋白质网络和基因型-表型关联来评估疾病风险。然而,复杂疾病风险预测的挑战仍然没有得到解决。在此,我们提出了一个基于Voronoi镶嵌网络分析来量化风险的框架,同时考虑了基因和变异的疾病关联分数。通过整合ClinVar、SNPnexus和DISEASES数据库,我们引入了一个基于成对疾病相关基因-变异分数的基因-变异图谱。使用Voronoi镶嵌和网络分析对该图谱进行聚类,并通过拟合背景Voronoi细胞密度分布获得阈值。我们根据基因-变异图谱上相关聚类内数据点的分数来定义疾病的相对风险。我们识别出可能在系统水平上相互作用的自身免疫相关聚类。所提出的框架可用于确定特定于复杂疾病亚型或促成多种亚型的聚类。