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Identification of lncRNA-disease association using bi-random walks

机译:使用双随机走行鉴定lncRNA-疾病关联

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There is evidence to suggest that lncRNAs are associated with distinct and diverse biological processes. The dysfunction or mutation of lncRNAs are implicated in a wide range of diseases. An accurate prediction of potential lncRNA-disease association can benefit the diagnosis of diseases and help us to gain a better understanding of the molecular mechanism. Although many related algorithms have been proposed, there still have much room for improvement. In this paper, we develop an algorithm, BiWalkLDA, to predict lncRNA-disease association by using bi-random walks. It constructs a lncRNA-disease network by integrating interaction profile and gene ontology information. Then, bi-random walks was applied to three real biological datasets. Results show that our method outperforms other algorithms in predicting lncRNA-disease association in terms of both accuracy and specificity. The source code of BiWalkLDA can be freely accessed at https://github.com/screamer/BiwalkLDA.
机译:有证据表明lncRNA与不同的生物过程有关。 lncRNA的功能障碍或突变与多种疾病有关。准确预测潜在的lncRNA-疾病关联可以有益于疾病的诊断,并有助于我们更好地了解分子机制。尽管已经提出了许多相关算法,但仍有很大的改进空间。在本文中,我们开发了一种算法BiWalkLDA,以通过使用双随机游走来预测lncRNA-疾病关联。它通过整合相互作用谱和基因本体信息来构建lncRNA疾病网络。然后,将双随机游走应用于三个真实的生物学数据集。结果表明,在准确性和特异性方面,我们的方法在预测lncRNA-疾病关联方面均优于其他算法。可以在https://github.com/screamer/BiwalkLDA上免费访问BiWalkLDA的源代码。

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