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Iteratively collective prediction of disease-gene associations through the incomplete network

机译:通过不完全网络迭代地集体预测疾病 - 基因关联

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The prediction of links between genes and disease is still one of the biggest challenges in the field of human health. Almost all state-of-the-art studies on the prediction of gene-disease links focuson a single pair of links, ignoring the associations and interactions among different types of links. Moreover, the biological information networks are usually incomplete. In this paper, we study the similarity measure to be used on two different types of nodes, based on the meta-paths between them (WSRM). Then an iterative self-updating approach for link prediction using heterogeneous information network is proposed to fit the incompletion of the network (ISL), which is a semi-supervised learning formula. Using the biological integrated network constructed from OMIM and HumanNet dataset (30,896 nodes and 1,200,166 edges) we applied our framework. The area under the receiver operating characteristic is 0.941, indicating that our approach significantly outperforms the state-of-the-art gene-disease link prediction approaches. Moreover, the sensitivity analysis signifies that our approach is robust. Consequently, our proposed framework demonstrates an efficient and accurate approach for link prediction between genes and diseases. In addition, during iteration, the accuracy of the result gradually increases. The example dataset and the implementation of our approach is avaliable at https://github.com/xymeng16/ISL.
机译:基因与疾病之间的链接预测仍然是人类健康领域的最大挑战之一。几乎所有关于预测基因疾病链接的最先进的研究侧重素,忽略不同类型的链路之间的关联和相互作用。此外,生物信息网络通常不完整。在本文中,我们基于它们之间的元路径(WSRM)来研究两个不同类型节点上的相似度措施。然后,提出了使用异构信息网络的链路预测的迭代自我更新方法,以适应网络(ISL)的不完整,这是一个半监督的学习公式。使用从OMIM和HUMANNET DataSet(30,896个节点和1,200,166个边缘)构建的生物集成网络,我们应用了我们的框架。接收器操作特性下的区域为0.941,表明我们的方法显着优于最先进的基因疾病链接预测方法。此外,敏感性分析表示我们的方法是强大的。因此,我们的拟议框架展示了基因和疾病之间的链路预测的有效和准确的方法。另外,在迭代期间,结果的准确性逐渐增加。示例数据集和我们的方法的实现是在https://github.com/xymeng16/isl中获得的。

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