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首页> 外文期刊>BMC Bioinformatics >An integrative network-based approach to identify novel disease genes and pathways: a case study in the context of inflammatory bowel disease
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An integrative network-based approach to identify novel disease genes and pathways: a case study in the context of inflammatory bowel disease

机译:基于综合网络的方法来鉴定新型疾病基因和途径:炎症性肠病背景下的案例研究

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There are different and complicated associations between genes and diseases. Finding the causal associations between genes and specific diseases is still challenging. In this work we present a method to predict novel associations of genes and pathways with inflammatory bowel disease (IBD) by integrating information of differential gene expression, protein-protein interaction and known disease genes related to IBD. We downloaded IBD gene expression data from NCBI's Gene Expression Omnibus, performed statistical analysis to determine differentially expressed genes, collected known IBD genes from DisGeNet database, which were used to construct a IBD related PPI network with HIPPIE database. We adapted our graph-based clustering algorithm DPClusO to cluster the disease PPI network. We evaluated the statistical significance of the identified clusters in the context of determining the richness of IBD genes using Fisher's exact test and predicted novel genes related to IBD. We showed 93.8% of our predictions are correct in the context of other databases and published literatures related to IBD. Finding disease-causing genes is necessary for developing drugs with synergistic effect targeting many genes simultaneously. Here we present an approach to identify novel disease genes and pathways and discuss our approach in the context of IBD. The approach can be generalized to find disease-associated genes for other diseases.
机译:基因和疾病之间存在不同和复杂的关联。寻找基因和特定疾病之间的因果关系仍然具有挑战性。在这项工作中,我们通过将鉴别基因表达,蛋白质 - 蛋白质相互作用和与IBD相关的已知疾病基因的信息集成来预测一种预测基因和途径与炎性肠病(IBD)的新缔组织和途径的方法。我们从NCBI的基因表达Omnibus下载了IBD基因表达数据,进行了统计分析以确定差异表达基因,从DISGenet数据库中收集已知的IBD基因,用于构建具有Hippie数据库的IBD相关的PPI网络。我们改编了基于图形的聚类算法DPCluso来聚类疾病PPI网络。我们在使用Fisher的确切测试和预测与IBD相关的新基因确定IBD基因的富含性的背景下,评估了所识别的簇的统计学意义。我们在其他数据库的背景下显示了93.8%的预测是正确的,并与IBD相关的文献。在同时靶向许多基因的具有协同作用的药物,寻找造成致病基因是必需的。在这里,我们提出了一种识别新型疾病基因和途径的方法,并在IBD的背景下讨论我们的方法。该方法可以推广以寻找其他疾病的疾病相关基因。

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