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Identification of drug-target interactions via fuzzy bipartite local model

机译:通过模糊二分局部模型鉴定药物靶靶相互作用

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摘要

With the emergence of large-scale experimental data on genes and proteins, drug discovery and repositioning will be more difficult in the field of biomedical research. More and more resources are needed for detecting drug-target interactions (DTIs) in the experimental works. The interactions between drugs and targets could been seen as a bipartite network. Many computational methods have been developed to identify DTIs. However, most of them did not integrate multiple information and filter noise or outlier points. In this paper, we develop a fuzzy bipartite local model (FBLM) based on fuzzy least squares support vector machine and multiple kernel learning (MKL) for predicting DTIs. First, multiple kernels are constructed in drug and target spaces, respectively. Then, all corresponding kernels are combined by MKL algorithm in two spaces. Finally, FBLM is employed to identify DTIs. Our proposed approach is tested on four benchmark datasets under three types of cross validation. Comparing with existing outstanding methods, our method is a useful tool for the DTIs prediction.
机译:随着对基因和蛋白质的大规模实验数据的出现,在生物医学研究领域,药物发现和重新定位将更加困难。检测实验工作中的药物靶标相互作用(DTI)需要越来越多的资源。药物和目标之间的相互作用可以被视为二分网络。已经开发了许多计算方法来识别DTI。但是,大多数都没有集成多个信息和滤波器噪声或异常值。在本文中,我们基于模糊最小二乘支持向量机和多个内核学习(MKL)来开发模糊二分的本地模型(FBLM),用于预测DTI。首先,分别以药物和靶空位构建多个核。然后,所有相应的内核通过两个空格中的MKL算法组合。最后,FBLM用于识别DTI。我们所提出的方法在三种基准数据集中进行三种类型的交叉验证测试。与现有的未完成方法相比,我们的方法是DTI预测的一个有用工具。

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