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首页> 外文期刊>IEEE/ACM transactions on computational biology and bioinformatics >NTSHMDA: Prediction of Human Microbe-Disease Association Based on Random Walk by Integrating Network Topological Similarity
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NTSHMDA: Prediction of Human Microbe-Disease Association Based on Random Walk by Integrating Network Topological Similarity

机译:NTSHMDA:通过整合网络拓扑相似性基于随机步行预测人类微生物疾病关联

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Accumulating clinic evidences have demonstrated that the microbes residing in human bodies play a significantly important role in the formation, development, and progression of various complex human diseases. Identifying latent related microbes for disease could provide insight into human disease mechanisms and promote disease prevention, diagnosis, and treatment. In this paper, we first construct a heterogeneous network by connecting the disease similarity network and the microbe similarity network through known microbe-disease association network, and then develop a novel computational model to predict human microbe-disease associations based on random walk by integrating network topological similarity (NTSHMDA). Specifically, each microbe-disease association pair is regarded as a distinct relationship level and, thus, assigned different weights based on network topological similarity. The experimental results show that NTSHMDA outperforms some state-of-the-art methods with average AUCs of 0.9070, 0.8896 +/- 0.0038 in the frameworks of Leave-one-out cross validation and 5-fold cross validation, respectively. In case studies, 9, 18, 38 and 9, 18, 45 out of top-10, 20, 50 candidate microbes are verified by recently published literatures for asthma and inflammatory bowel disease, respectively. In conclusion, NTSHMDA has potential ability to identify novel disease-microbe associations and can also provide valuable information for drug discovery and biological researches.
机译:积累的诊所证据表明,居住在人体中的微生物在各种复杂人类疾病的形成,开发和进展中起着显着重要的作用。鉴定潜在的疾病微生物可以提供对人类疾病机制的洞察力,促进疾病预防,诊断和治疗。在本文中,我们首先通过通过已知的微生物疾病关联网络连接疾病相似性网络和微生物相似性网络来构建异质网络,然后开发一种新的计算模型,通过集成网络基于随机步行来预测人类微生物疾病关联拓扑相似性(NTSHMDA)。具体地,每个微生物疾病关联对被视为不同的关系水平,因此基于网络拓扑相似性分配不同的权重。实验结果表明,NTSHMDA分别优于一些最先进的方法,平均AUC为0.9070,0.9070,0.8896 +/- 0.0038,分别在休假交叉验证和5倍交叉验证的框架中。在最近公开的哮喘和炎性肠病的文献中,在前10,20,50,50℃下的9,18,38和9,18,45分别通过用于哮喘和炎性肠病疾病的文献来验证。总之,NTSHMDA具有识别新型疾病 - 微生物协会的潜力能力,也可以为药物发现和生物研究提供有价值的信息。

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