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Inferring Candidate CircRNA-Disease Associations by Bi-random Walk Based on CircRNA Regulatory Similarity

机译:基于CircRNA调控相似性的双随机步行推断候选CircRNA疾病关联。

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Identification of associations between circular RNAs (circRNA) and diseases has become a hot topic, which is beneficial for researchers to understand the disease mechanism. However, traditional biological experiments are expensive and time-consuming. In this study, we proposed a novel method named BWHCDA, which applied bi-random walk algorithm on the heterogeneous network for predicting circRNA-disease associations. First, circRNA regulatory similarity is measured based on circRNA-miRNA interactions, and circRNA similarity is calculated by the average of circRNA regulatory similarity and Gaussian interaction profiles (GIP) kernel similarity for circRNAs. Similarly, disease similarity is the mean of disease semantic similarity and GIP kernel similarity for diseases. Then, the heterogeneous network is constructed by integrating circRNA network, disease network via circRNA-disease associations. Subsequently, the bi-random walk algorithm is implemented on the heterogeneous network to predict circRNA-disease associations. Finally, we utilize leave-one-out cross validation and 10-fold cross validation frameworks to evaluate the prediction performance of BWHCDA method and obtain AUC of 0.9334 and 0.8764 ± 0.0038, respectively. Moreover, the predicted hsa_circ_0000519-gastric cancer association is analyzed. Results show that BWHCDA could be an effective resource for clinical experimental guidance.
机译:环状RNA(circRNA)与疾病之间的关联的鉴定已成为一个热门话题,这对研究人员了解疾病的发病机理是有益的。然而,传统的生物学实验是昂贵且费时的。在这项研究中,我们提出了一种称为BWHCDA的新方法,该方法在异构网络上应用了双向随机游走算法来预测circRNA-疾病关联。首先,基于circRNA-miRNA相互作用测量circRNA调节相似性,并通过circRNA的circRNA调节相似性和高斯相互作用谱(GIP)内核相似性的平均值来计算circRNA相似性。同样,疾病相似性是疾病的语义相似性和GIP内核相似性的平均值。然后,通过circRNA-疾病关联,通过整合circRNA网络,疾病网络来构建异构网络。随后,在异质网络上实施双随机行走算法以预测circRNA-疾病关联。最后,我们利用留一法交叉验证和10折交叉验证框架来评估BWHCDA方法的预测性能,并分别获得0.9334和0.8764±0.0038的AUC。此外,分析了预测的hsa_circ_0000519-胃癌关联。结果表明,BWHCDA可以作为临床实验指导的有效资源。

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