MLFLHMDA: predicting human microbe-disease association based on multi-view latent feature learning

被引:2
|
作者
Chen, Ziwei [1 ]
Zhang, Liangzhe [1 ]
Li, Jingyi [1 ]
Fu, Mingyang [1 ]
机构
[1] Beijing Jiaotong Univ, Sch Elect & Informat Engn, Beijing, Peoples R China
关键词
microbe; disease; microbe-disease association; multi-view; latent feature learning; CLOSTRIDIUM-SEPTICUM; GUT MICROBIOTA;
D O I
10.3389/fmicb.2024.1353278
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Introduction A growing body of research indicates that microorganisms play a crucial role in human health. Imbalances in microbial communities are closely linked to human diseases, and identifying potential relationships between microbes and diseases can help elucidate the pathogenesis of diseases. However, traditional methods based on biological or clinical experiments are costly, so the use of computational models to predict potential microbe-disease associations is of great importance.Methods In this paper, we present a novel computational model called MLFLHMDA, which is based on a Multi-View Latent Feature Learning approach to predict Human potential Microbe-Disease Associations. Specifically, we compute Gaussian interaction profile kernel similarity between diseases and microbes based on the known microbe-disease associations from the Human Microbe-Disease Association Database and perform a preprocessing step on the resulting microbe-disease association matrix, namely, weighting K nearest known neighbors (WKNKN) to reduce the sparsity of the microbe-disease association matrix. To obtain unobserved associations in the microbe and disease views, we extract different latent features based on the geometrical structure of microbes and diseases, and project multi-modal latent features into a common subspace. Next, we introduce graph regularization to preserve the local manifold structure of Gaussian interaction profile kernel similarity and add L p , q -norms to the projection matrix to ensure the interpretability and sparsity of the model.Results The AUC values for global leave-one-out cross-validation and 5-fold cross validation implemented by MLFLHMDA are 0.9165 and 0.8942+/-0.0041, respectively, which perform better than other existing methods. In addition, case studies of different diseases have demonstrated the superiority of the predictive power of MLFLHMDA. The source code of our model and the data are available on https://github.com/LiangzheZhang/MLFLHMDA_master.
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页数:12
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