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A spectral analysis and network science approach to identify influential diseases based on disease-gene associations

机译:基于疾病-基因关联的频谱分析和网络科学方法来确定有影响的疾病

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摘要

We model a disease-disease network as an undirected graph of diseases (vertices) wherein two vertices are connected with an edge if the corresponding diseases have one or more common associated genes (the number of common genes is the weight of the edge). In such a weighted graph, a disease with a larger number of common genes with several other diseases is more likely to incur a higher eigenvector centrality (EVC). Our hypothesis is that a person with a higher EVC disease is more likely to acquire other related diseases compared to a person with a lower EVC disease. We tested our hypothesis on the disease-disease network constructed from the results of the disease-gene association studies reported in the NIH GWAS catalogue and OMIM database. The disease EVC values exhibited a Pareto distribution (80-20 rule): around 18% of the diseases have larger and significantly different EVC values and the remaining 82% of the diseases had lower and similar EVC values. This implies that around 18% of the diseases in humans are more likely to have a larger likelihood of leading to other diseases.
机译:我们将疾病-疾病网络建模为疾病(顶点)的无向图,其中,如果相应的疾病具有一个或多个共同的相关基因(共同基因的数量是边缘的权重),则两个顶点与边缘相连。在这样的加权图中,具有更多共同基因的疾病与其他几种疾病的疾病更有可能导致更高的特征向量中心度(EVC)。我们的假设是,与EVC疾病较低的人相比,EVC疾病较高的人更容易患其他相关疾病。我们根据由NIH GWAS目录和OMIM数据库中报告的疾病-基因关联研究的结果构建的疾病-疾病网络,检验了我们的假设。疾病的EVC值表现出帕累托分布(80-20法则):大约18%的疾病具有更大且显着不同的EVC值,其余82%的疾病具有较低且相似的EVC值。这意味着人类中大约18%的疾病更有可能导致其他疾病。

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