A Drug Repositioning Approach Using Drug and Disease Features

Jialan Tang, Baiying Lei, Weilin Chen
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Abstract

Drug repositioning is an important method in drug discovery. Experiment-based drug discovery is time-consuming and expensive. In recent years, methods based on heterogeneous networks have attracted research interest in this area due to the advantages in this task. By adding features fused from different drug networks and disease features mined from biomedical texts, the prediction effect can be improved. This paper proposes a drug repositioning method using the multi-modal deep autoencoder (MDA) method, which obtains better drug features after fusing several drug networks. Then, in order to predict the links between drug and diseases, disease traits are taken from the text data of biomedical information and combined with the known drug-disease combinations. Specifically, after feature fusion using MDA method, we also use a sparse multi-layer autoencoder (SMAE) to obtain low-dimensional and high-quality drug vector representation, and prove the effectiveness of SMAE module in our ablation experiment. Experimental results indicate that this model can outperform existing methods.
利用药物和疾病特征的药物重新定位方法
药物重新定位是药物发现的重要方法。基于实验的药物发现既耗时又昂贵。近年来,基于异构网络的方法由于其在任务中的优势而引起了该领域的研究兴趣。通过加入不同药物网络融合的特征和从生物医学文本中挖掘的疾病特征,可以提高预测效果。本文提出了一种基于多模态深度自编码器(MDA)方法的药物重新定位方法,该方法在融合多个药物网络后获得更好的药物特征。然后,从生物医学信息的文本数据中提取疾病特征,并结合已知的药物-疾病组合,预测药物与疾病之间的联系。具体来说,在使用MDA方法进行特征融合后,我们还使用稀疏多层自编码器(SMAE)获得低维高质量的药物向量表示,并在消融实验中证明了SMAE模块的有效性。实验结果表明,该模型优于现有的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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