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GRTR: Drug-Disease Association Prediction Based on Graph Regularized Transductive Regression on Heterogeneous Network

机译:GRTR:异质网络上基于图正则化转导回归的药物-疾病关联预测

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Computational drug repositioning helps to decipher the complex relations among drugs, targets, and diseases at a system level. However, most existing computational methods are biased towards known drugs-disease associations already verified by biological experiments. It is difficult to achieve excellent performance with sparse known drug-disease associations. In this article, we present a graph regularized transductive regression method (GRTR) to predict novel drug-disease associations. The proposed method first constructs a heterogeneous graph consisting of three interlinked sub-graphs including drugs, diseases and targets from multiple sources and adopts preliminary estimation of drug-related disease to initial unknown drug-disease associations for unlabeled drugs. Since the known drug-disease associations are sparse, graph regularized transductive regression is used to score and rank drug-disease associations iteratively. In the computational experiments, the proposed method achieves better performance than others in terms of AUC and AUPR. Moreover, the varying of parameters is shown to verify the importance of preliminary estimation in GRTR. Case studies on several selected drugs further confirm the practicality of our method in discovering potential indications for drugs.
机译:计算药物的重新定位有助于在系统级别上解析药物,靶标和疾病之间的复杂关系。然而,大多数现有的计算方法偏向于已经由生物学实验证实的已知药物-疾病关联。稀疏的已知药物-疾病关联很难实现出色的性能。在本文中,我们提出了一种图形正则化的转导回归方法(GRTR)来预测新型药物-疾病关联。所提出的方法首先构造一个由三个相互联系的子图组成的异构图,包括来自多个来源的药物,疾病和靶标,并采用药物相关疾病的初步估计与未标记药物的初始未知药物-疾病关联。由于已知的药物-疾病关联稀疏,因此使用图正则化的转导回归来迭代地对药物-疾病关联进行评分和排名。在计算实验中,所提出的方法在AUC和AUPR方面取得了比其他方法更好的性能。此外,显示了参数的变化以验证GRTR中初步估计的重要性。对几种选定药物的案例研究进一步证实了我们方法在发现药物潜在适应症方面的实用性。

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