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A Novel Network-Based Computational Model for Prediction of Potential LncRNA–Disease Association

机译:一种新型的基于网络的潜在LncRNA-疾病关联预测计算模型。

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摘要

Accumulating studies have shown that long non-coding RNAs (lncRNAs) are involved in many biological processes and play important roles in a variety of complex human diseases. Developing effective computational models to identify potential relationships between lncRNAs and diseases can not only help us understand disease mechanisms at the lncRNA molecular level, but also promote the diagnosis, treatment, prognosis, and prevention of human diseases. For this paper, a network-based model called NBLDA was proposed to discover potential lncRNA–disease associations, in which two novel lncRNA–disease weighted networks were constructed. They were first based on known lncRNA–disease associations and topological similarity of the lncRNA–disease association network, and then an lncRNA–lncRNA weighted matrix and a disease–disease weighted matrix were obtained based on a resource allocation strategy of unequal allocation and unbiased consistence. Finally, a label propagation algorithm was applied to predict associated lncRNAs for the investigated diseases. Moreover, in order to estimate the prediction performance of NBLDA, the framework of leave-one-out cross validation (LOOCV) was implemented on NBLDA, and simulation results showed that NBLDA can achieve reliable areas under the ROC curve (AUCs) of 0.8846, 0.8273, and 0.8075 in three known lncRNA–disease association datasets downloaded from the lncRNADisease database, respectively. Furthermore, in case studies of lung cancer, leukemia, and colorectal cancer, simulation results demonstrated that NBLDA can be a powerful tool for identifying potential lncRNA–disease associations as well.
机译:越来越多的研究表明,长的非编码RNA(lncRNA)参与许多生物过程,并在多种复杂的人类疾病中发挥重要作用。开发有效的计算模型以识别lncRNA与疾病之间的潜在关系,不仅可以帮助我们了解lncRNA分子水平上的疾病机制,而且可以促进人类疾病的诊断,治疗,预后和预防。在本文中,提出了一种基于网络的模型NBLDA,以发现潜在的lncRNA-疾病关联,其中构建了两个新颖的lncRNA-疾病加权网络。它们首先基于已知的lncRNA-疾病关联和lncRNA-疾病关联网络的拓扑相似性,然后基于不平等分配和无偏一致性的资源分配策略获得了lncRNA-lncRNA加权矩阵和疾病-疾病加权矩阵。 。最后,将标签传播算法应用于预测所研究疾病的相关lncRNA。此外,为了评估NBLDA的预测性能,在NBLDA上实施了留一法交叉验证(LOOCV)框架,仿真结果表明NBLDA可以在0.8846的ROC曲线(AUC)下获得可靠的面积,从lncRNADisease数据库下载的三个已知的lncRNA-疾病关联数据集中的数据分别为0.8273和0.8075。此外,在肺癌,白血病和大肠癌的案例研究中,模拟结果表明,NBLDA也是识别潜在的lncRNA与疾病关联的有力工具。

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