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Predicting Adverse Drug-Drug Interactions via Semi-supervised Variational Autoencoders

机译:通过半监督变分性自身偏析预测不良药物 - 药物相互作用

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Adverse Drug-Drug Interactions (DDIs) are a very important risk factor in the medical process, which may lead to readmission or death. Although a part of DDIs can be obtained through in vitro or in vivo experiments in the drug development stage, a large number of new DDIs still appear after the market, more and more researchers begin to pay attention to the research related to drug molecules, such as drug discovery, drug target prediction, DDIs prediction, etc. In recent years, many computational methods for predicting DDIs have been proposed. However, most of them only used labeled data and neglect a lot of information hidden in unlabeled data. Moreover, they always focus on binary prediction instead of multiclass prediction, although the exact DDI type is very helpful for our reasonable choice of medication. In this paper, a Semi-Surpervised Variational Autoencoders (SPRAT) method for predicting DDIs is proposed, which is composed of a neural network classifier and a Variational autoencoders (VAE). Classifier is the core components, VAE plays a role of calibration. In the end, the predicted label is a multi-hot vector which indicates specific DDI types between drug pairs. Finally, the experiments on real world dataset demonstrate the effectiveness of the proposed method in this paper.
机译:不良药物 - 药物相互作用(DDIS)是医疗过程中的一个非常重要的风险因素,可能导致入院或死亡。尽管DDIS的一部分可以通过体外或体内实验在药物开发阶段获得,但市场仍然出现了大量的新DDIS,越来越多的研究人员开始关注与药物分子相关的研究,如作为药物发现,药物目标预测,DDIS预测等近年来,已经提出了用于预测DDI的许多计算方法。但是,它们中的大多数仅使用标记数据并忽略隐藏在未标记数据中的大量信息。此外,它们始终专注于二进制预测而不是多字母预测,尽管确切的DDI类型对于我们合理选择的药物非常有帮助。在本文中,提出了一种用于预测DDIS的半递变分别自动沉积物(SPRAT)方法,其由神经网络分类器和变形自动化器(VAE)组成。分类器是核心组件,VAE起校准的作用。最后,预测标签是一种多热量矢量,其指示药物对之间的特定DDI类型。最后,现实世界数据集的实验证明了本文提出的方法的有效性。

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