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首页> 外文期刊>Artificial intelligence in medicine >Predicting human immunodeficiency virus inhibitors using multi-dimensional Bayesian network classifiers
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Predicting human immunodeficiency virus inhibitors using multi-dimensional Bayesian network classifiers

机译:使用多维贝叶斯网络分类器预测人类免疫缺陷病毒抑制剂

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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.
机译:目的:我们的目标是使用多维贝叶斯网络分类器,以预测输入了HIV患者携带的各个耐药突变的输入集的人类1型免疫缺陷病毒(HIV-1)逆转录酶和蛋白酶抑制剂的水平。材料和方法:多维贝叶斯网络分类器(MBC)是专门为解决多维分类问题而设计的概率图形模型,其中必须将数据集中的每个输入实例同时分配给多个不一定是二进制的输出类变量。在本文中,我们引入了一种名为mb-mbc的新方法,该方法通过使用HITON算法确定每个类变量周围的马尔可夫覆盖范围来从数据中学习MBC。我们的方法适用于从Stanford HIV-1数据库获得的逆转录酶和蛋白酶数据集。结果:关于抗逆转录病毒联合疗法的预测,与最新的MBC学习算法相比,实验研究在分类准确性方面显示出可喜的结果。对于逆转录酶抑制剂,我们的平均准确度和整体准确度分别为71%和11%;而蛋白酶抑制剂的平均准确度和整体准确度分别超过84%和31%。此外,MBC图形结构的分析使我们能够洞悉逆转录酶和蛋白酶抑制剂之间的已知相互作用和新型相互作用以及它们各自的抗性突变。结论:mb-mbc算法是分析HIV-1逆转录酶和蛋白酶抑制剂预测问题以及发现这两类抑制剂内部和之间相互作用的宝贵工具。

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