Yu Limin, Shen Xianjun, Zhong Duo, Yang Jincai
School of Computer, Central China Normal University, Wuhan, China.
Hubei Provincial Key Laboratory of Artificial Intelligence and Smart Learning, Central China Normal University, Wuhan, China.
Front Genet. 2020 Jan 10;10:1316. doi: 10.3389/fgene.2019.01316. eCollection 2019.
miRNA plays an important role in many biological processes, and increasing evidence shows that miRNAs are closely related to human diseases. Most existing miRNA-disease association prediction methods were only based on data related to miRNAs and diseases and failed to effectively use other existing biological data. However, experimentally verified miRNA-disease associations are limited, there are complex correlations between biological data. Therefore, we propose a novel Three-layer heterogeneous network Combined with unbalanced Random Walk for MiRNA-Disease Association prediction algorithm (TCRWMDA), which can effectively integrate multi-source association data. TCRWMDA based not only on the known miRNA-disease associations, also add the new priori information (lncRNA-miRNA and lncRNA-disease associations) to build a three-layer heterogeneous network, lncRNA was added as the transition path of the intermediate point to mine more effective information between networks. The AUC value obtained by the TCRWMDA algorithm on 5-fold cross validation is 0.9209, compared with other models based on the same similarity calculation method, TCRWMDA obtained better results. TCRWMDA was applied to the analysis of four types of cancer, the results proved that TCRWMDA is an effective tool to predict the potential miRNA-disease association. The source code and dataset of TCRWMDA are available at: https://github.com/ylm0505/TCRWMDA.
微小RNA(miRNA)在许多生物学过程中发挥着重要作用,越来越多的证据表明miRNA与人类疾病密切相关。大多数现有的miRNA-疾病关联预测方法仅基于与miRNA和疾病相关的数据,未能有效利用其他现有的生物学数据。然而,经实验验证的miRNA-疾病关联有限,生物学数据之间存在复杂的相关性。因此,我们提出了一种新颖的结合非平衡随机游走的三层异质网络用于miRNA-疾病关联预测算法(TCRWMDA),该算法可以有效地整合多源关联数据。TCRWMDA不仅基于已知的miRNA-疾病关联,还添加了新的先验信息(lncRNA-miRNA和lncRNA-疾病关联)来构建三层异质网络,添加lncRNA作为中间点的过渡路径以挖掘网络之间更有效的信息。TCRWMDA算法在5折交叉验证中获得的AUC值为0.9209,与基于相同相似性计算方法的其他模型相比,TCRWMDA取得了更好的结果。TCRWMDA应用于四种癌症类型的分析,结果证明TCRWMDA是预测潜在miRNA-疾病关联的有效工具。TCRWMDA的源代码和数据集可在以下网址获取:https://github.com/ylm0505/TCRWMDA 。