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Ranking Transitive Chemical-Disease Inferences Using Local Network Topology in the Comparative Toxicogenomics Database

机译:排名在比较毒理基因组学数据库使用本地网络拓扑传递化学疾病推论

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摘要

Exposure to chemicals in the environment is believed to play a critical role in the etiology of many human diseases. To enhance understanding about environmental effects on human health, the Comparative Toxicogenomics Database (CTD; ) provides unique curated data that enable development of novel hypotheses about the relationships between chemicals and diseases. CTD biocurators read the literature and curate direct relationships between chemicals-genes, genes-diseases, and chemicals-diseases. These direct relationships are then computationally integrated to create additional inferred relationships; for example, a direct chemical-gene statement can be combined with a direct gene-disease statement to generate a chemical-disease inference (inferred via the shared gene). In CTD, the number of inferences has increased exponentially as the number of direct chemical, gene and disease interactions has grown. To help users navigate and prioritize these inferences for hypothesis development, we implemented a statistic to score and rank them based on the topology of the local network consisting of the chemical, disease and each of the genes used to make an inference. In this network, chemicals, diseases and genes are nodes connected by edges representing the curated interactions. Like other biological networks, node connectivity is an important consideration when evaluating the CTD network, as the connectivity of nodes follows the power-law distribution. Topological methods reduce the influence of highly connected nodes that are present in biological networks. We evaluated published methods that used local network topology to determine the reliability of protein–protein interactions derived from high-throughput assays. We developed a new metric that combines and weights two of these methods and uniquely takes into account the number of common neighbors and the connectivity of each entity involved. We present several CTD inferences as case studies to demonstrate the value of this metric and the biological relevance of the inferences.
机译:人们认为,在环境中接触化学物质在许多人类疾病的病因中起着至关重要的作用。为了加深对环境对人类健康的影响的理解,比较毒物基因组学数据库(CTD;)提供了独特的精选数据,这些数据使得能够开发出有关化学物质与疾病之间关系的新颖假设。 CTD生物管理者阅读文献并策划化学物质-基因,基因疾病和化学物质-疾病之间的直接关系。然后将这些直接关系进行计算集成以创建其他推断关系;例如,可以将直接化学基因陈述与直接基因疾病陈述相结合以生成化学疾病推断(通过共享基因推断)。在CTD中,随着直接化学,基因和疾病相互作用的数量增加,推断的数量呈指数增长。为了帮助用户导航和优先考虑这些推论,以进行假设开发,我们基于由化学,疾病和用于推论的每个基因组成的本地网络的拓扑结构,实施了统计数据以对它们进行评分和排名。在这个网络中,化学物质,疾病和基因是由代表策划的相互作用的边缘相连的节点。像其他生物网络一样,在评估CTD网络时,节点连接性也是一个重要的考虑因素,因为节点的连接性遵循幂律分布。拓扑方法减少了生物网络中存在的高度连接的节点的影响。我们评估了已发布的方法,这些方法使用本地网络拓扑来确定从高通量分析得出的蛋白质间相互作用的可靠性。我们开发了一种新指标,将两种方法结合并加权,并唯一考虑了公共邻居的数量以及所涉及的每个实体的连通性。我们以案例研究的形式介绍了几种CTD推论,以证明该指标的价值以及推论的生物学相关性。

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