Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pcbi.1004760
Title: Neighborhood Regularized Logistic Matrix Factorization for Drug-Target Interaction Prediction
Authors: Liu Y.
Wu M.
Miao C.
Zhao P.
Li X.-L. 
Keywords: cell nucleus receptor
enzyme
G protein coupled receptor
ion channel
drug
ligand
protein
accuracy
algorithm
area under the curve
area under the precision recall curve
Article
controlled study
drug target interaction
drug targeting
information processing
neighborhood regularized logistic matrix factorization
observation
prediction
probability
receiver operating characteristic
statistical concepts
algorithm
biology
chemistry
drug development
metabolism
procedures
Algorithms
Computational Biology
Drug Discovery
Ligands
Pharmaceutical Preparations
Proteins
Issue Date: 2016
Citation: Liu Y., Wu M., Miao C., Zhao P., Li X.-L. (2016). Neighborhood Regularized Logistic Matrix Factorization for Drug-Target Interaction Prediction. PLoS Computational Biology 12 (2) : e1004760. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pcbi.1004760
Rights: Attribution 4.0 International
Abstract: In pharmaceutical sciences, a crucial step of the drug discovery process is the identification of drug-target interactions. However, only a small portion of the drug-target interactions have been experimentally validated, as the experimental validation is laborious and costly. To improve the drug discovery efficiency, there is a great need for the development of accurate computational approaches that can predict potential drug-target interactions to direct the experimental verification. In this paper, we propose a novel drug-target interaction prediction algorithm, namely neighborhood regularized logistic matrix factorization (NRLMF). Specifically, the proposed NRLMF method focuses on modeling the probability that a drug would interact with a target by logistic matrix factorization, where the properties of drugs and targets are represented by drug-specific and target-specific latent vectors, respectively. Moreover, NRLMF assigns higher importance levels to positive observations (i.e., the observed interacting drug-target pairs) than negative observations (i.e., the unknown pairs). Because the positive observations are already experimentally verified, they are usually more trustworthy. Furthermore, the local structure of the drug-target interaction data has also been exploited via neighborhood regularization to achieve better prediction accuracy. We conducted extensive experiments over four benchmark datasets, and NRLMF demonstrated its effectiveness compared with five state-of-the-art approaches. ? 2016 Liu et al.
Source Title: PLoS Computational Biology
URI: https://scholarbank.nus.edu.sg/handle/10635/161924
ISSN: 1553734X
DOI: 10.1371/journal.pcbi.1004760
Rights: Attribution 4.0 International
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