A Novel Triple Matrix Factorization Method for Detecting Drug-Side Effect Association Based on Kernel Target Alignment.

All drugs usually have side effects, which endanger the health of patients. To identify potential side effects of drugs, biological and pharmacological experiments are done but are expensive and time-consuming. So, computation-based methods have been developed to accurately and quickly predict side...

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Publicado en:BioMed Research International pp. 1 - 12
Autores principales: Guo, Xiaoyi, Zhou, Wei, Yu, Yan, Ding, Yijie, Tang, Jijun, Guo, Fei
Formato: equations & formulas pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 5/29/2020
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 5/29/2020
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2020/4675395
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        atl: A Novel Triple Matrix Factorization Method for Detecting Drug-Side Effect Association Based on Kernel Target Alignment.
      aug:
        au:
          Guo, Xiaoyi
          Zhou, Wei
          Yu, Yan
          Ding, Yijie
          Tang, Jijun
          Guo, Fei
        affil: The Hemodialysis Center, The Affiliated Wuxi People's Hospital of Nanjing Medical University, 214000 Wuxi, China
      sug:
        subj:
          Models, Statistical
          Drug Toxicity Diagnosis
          Human
          Comparative Studies
          Validity
          Benchmarking
          Computer Simulation
          Molecular Structure
      ab: All drugs usually have side effects, which endanger the health of patients. To identify potential side effects of drugs, biological and pharmacological experiments are done but are expensive and time-consuming. So, computation-based methods have been developed to accurately and quickly predict side effects. To predict potential associations between drugs and side effects, we propose a novel method called the Triple Matrix Factorization- (TMF-) based model. TMF is built by the biprojection matrix and latent feature of kernels, which is based on Low Rank Approximation (LRA). LRA could construct a lower rank matrix to approximate the original matrix, which not only retains the characteristics of the original matrix but also reduces the storage space and computational complexity of the data. To fuse multivariate information, multiple kernel matrices are constructed and integrated via Kernel Target Alignment-based Multiple Kernel Learning (KTA-MKL) in drug and side effect space, respectively. Compared with other methods, our model achieves better performance on three benchmark datasets. The values of the Area Under the Precision-Recall curve (AUPR) are 0.677, 0.685, and 0.680 on three datasets, respectively.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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