Predicting human immunodeficiency virus inhibitors using multi-dimensional. Bayesian network classifiers

被引:32
作者
Borchani, Hanen [1 ]
Bielza, Concha [1 ]
Toro, Carlos [2 ]
Larranaga, Pedro [1 ]
机构
[1] Univ Politecn Madrid, Fac Informat, Dept Inteligencia Artificial, Computat Intelligence Grp, Boadilla Del Monte 28660, Spain
[2] Hosp Carlos III, Dept Microbiol, Madrid 28029, Spain
关键词
Multi-dimensional Bayesian network classifiers; Markov blanket; Human immunodeficiency virus; Protease inhibitors; Reverse transcriptase inhibitors; MARKOV BLANKET INDUCTION; REVERSE-TRANSCRIPTASE; RESISTANCE PATHWAYS; FEATURE-SELECTION; CAUSAL DISCOVERY; LOCAL CAUSAL; COMBINATION; MUTATIONS; TYPE-1;
D O I
10.1016/j.artmed.2012.12.005
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Objective: Our aim is to use multi-dimensional Bayesian network classifiers in order to predict the human immunodeficiency virus type 1 (HIV-1) reverse transcriptase and protease inhibitors given an input set of respective resistance mutations that an HIV patient carries. Materials and methods: Multi-dimensional Bayesian network classifiers (MBCs) are probabilistic graphical models especially designed to solve multi-dimensional classification problems, where each input instance in the data set has to be assigned simultaneously to multiple output class variables that are not necessarily binary. In this paper, we introduce a new method, named MB-MBC, for learning MBCs from data by determining the Markov blanket around each class variable using the HITON algorithm. Our method is applied to both reverse transcriptase and protease data sets obtained from the Stanford HIV-1 database. Results: Regarding the prediction of antiretroviral combination therapies, the experimental study shows promising results in terms of classification accuracy compared with state-of-the-art MBC learning algorithms. For reverse transcriptase inhibitors, we get 71% and 11% in mean and global accuracy, respectively: while for protease inhibitors, we get more than 84% and 31% in mean and global accuracy, respectively. In addition, the analysis of MBC graphical structures lets us gain insight into both known and novel interactions between reverse transcriptase and protease inhibitors and their respective resistance mutations. Conclusion: MB-MBC algorithm is a valuable tool to analyze the HIV-1 reverse transcriptase and protease inhibitors prediction problem and to discover interactions within and between these two classes of inhibitors. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:219 / 229
页数:11
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