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首页> 外文期刊>BMC Systems Biology >KDiamend: a package for detecting key drivers in a molecular ecological network of disease
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KDiamend: a package for detecting key drivers in a molecular ecological network of disease

机译:KDiamend:一种用于检测疾病分子生态网络中关键驱动因素的软件包

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Microbial abundance profiles are applied widely to understand diseases from the aspect of microbial communities. By investigating the abundance associations of species or genes, we can construct molecular ecological networks (MENs). The MENs are often constructed by calculating the Pearson correlation coefficient (PCC) between genes. In this work, we also applied multimodal mutual information (MMI) to construct MENs. The members which drive the concerned MENs are referred to as key drivers. We proposed a novel method to detect the key drivers. First, we partitioned the MEN into subnetworks. Then we identified the most pertinent subnetworks to the disease by measuring the correlation between the abundance pattern and the delegated phenotype—the variable representing the disease phenotypes. Last, for each identified subnetwork, we detected the key driver by PageRank. We developed a package named KDiamend and applied it to the gut and oral microbial data to detect key drivers for Type 2 diabetes (T2D) and Rheumatoid Arthritis (RA). We detected six T2D-relevant subnetworks and three key drivers of them are related to the carbohydrate metabolic process. In addition, we detected nine subnetworks related to RA, a disease caused by compromised immune systems. The extracted subnetworks include InterPro matches (IPRs) concerned with immunoglobulin, Sporulation, biofilm, Flaviviruses, bacteriophage, etc., while the development of biofilms is regarded as one of the drivers of persistent infections. KDiamend is feasible to detect key drivers and offers insights to uncover the development of diseases. The package is freely available at http://www.deepomics.org/pipelines/3DCD6955FEF2E64A/ .
机译:微生物丰度概况被广泛用于从微生物群落的角度了解疾病。通过研究物种或基因的丰富关联,我们可以构建分子生态网络(MENs)。 MEN通常是通过计算基因之间的Pearson相关系数(PCC)来构建的。在这项工作中,我们还应用了多模式互信息(MMI)来构建MEN。驱动相关MEN的成员称为关键驱动器。我们提出了一种新颖的方法来检测关键驱动程序。首先,我们将MEN划分为子网。然后,我们通过测量丰度模式与委托表型(代表疾病表型的变量)之间的相关性,来确定与疾病最相关的子网。最后,对于每个确定的子网,我们通过PageRank检测到了关键驱动程序。我们开发了名为KDiamend的软件包,并将其应用于肠道和口腔微生物数据,以检测2型糖尿病(T2D)和类风湿关节炎(RA)的关键驱动因素。我们检测到六个与T2D相关的子网,其中三个关键驱动因素与碳水化合物的代谢过程有关。此外,我们检测到9个与RA相关的子网,RA是由免疫系统受损引起的疾病。提取的子网包括与免疫球蛋白,孢子形成,生物膜,黄病毒,噬菌体等有关的InterPro匹配(IPR),而生物膜的发展被认为是持续感染的驱动因素之一。 KDiamend可用于检测关键驱动因素,并提供洞察力以发现疾病的发展。该软件包可从http://www.deepomics.org/pipelines/3DCD6955FEF2E64A/​​免费获得。

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