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IDSSIM: an lncRNA functional similarity calculation model based on an improved disease semantic similarity method

机译:IDSSIM:基于改进疾病语义相似方法的LNCRNA功能相似性计算模型

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It has been widely accepted that long non-coding RNAs (lncRNAs) play important roles in the development and progression of human diseases. Many association prediction models have been proposed for predicting lncRNA functions and identifying potential lncRNA-disease associations. Nevertheless, among them, little effort has been attempted to measure lncRNA functional similarity, which is an essential part of association prediction models. In this study, we presented an lncRNA functional similarity calculation model, IDSSIM for short, based on an improved disease semantic similarity method, highlight of which is the introduction of information content contribution factor into the semantic value calculation to take into account both the hierarchical structures of disease directed acyclic graphs and the disease specificities. IDSSIM and three state-of-the-art models, i.e., LNCSIM1, LNCSIM2, and ILNCSIM, were evaluated by applying their disease semantic similarity matrices and the lncRNA functional similarity matrices, as well as corresponding matrices of human lncRNA-disease associations coming from either lncRNADisease database or MNDR database, into an association prediction method WKNKN for lncRNA-disease association prediction. In addition, case studies of breast cancer and adenocarcinoma were also performed to validate the effectiveness of IDSSIM. Results demonstrated that in terms of ROC curves and AUC values, IDSSIM is superior to compared models, and can improve accuracy of disease semantic similarity effectively, leading to increase the association prediction ability of the IDSSIM-WKNKN model; in terms of case studies, most of potential disease-associated lncRNAs predicted by IDSSIM can be confirmed by databases and literatures, implying that IDSSIM can serve as a promising tool for predicting lncRNA functions, identifying potential lncRNA-disease associations, and pre-screening candidate lncRNAs to perform biological experiments. The IDSSIM code, all experimental data and prediction results are available online at https://github.com/CDMB-lab/IDSSIM .
机译:已普遍接受,长期非编码RNA(LNCRNA)在人类疾病的发展和进展中起重要作用。已经提出了许多关联预测模型,用于预测LNCRNA功能并鉴定潜在的LNCRNA疾病关联。然而,其中,已经尝试测量LNCRNA功能相似性的很少努力,这是关联预测模型的重要组成部分。在本研究中,我们介绍了一种LNCRNA功能相似性计算模型,IDSSIM短,基于改进的疾病语义相似性方法,突出显示,它是将信息内容贡献因子引入语义价值计算,以考虑分层结构疾病指向无循环图和疾病特异性。通过应用疾病语义相似性矩阵和LNCRNA功能相似性矩阵来评估IDSSIM和三种最先进的模型,即LNCSIM1,LNCSIM2和ILNCSIM,以及来自的人LNCRNA疾病关联的相应矩阵LNCRNAdisease数据库或MNDR数据库,进入LNCRNA疾病关联预测的关联预测方法WKNKN。此外,还进行了对乳腺癌和腺癌的案例研究,以验证IDSSIM的有效性。结果表明,就ROC曲线和AUC值而言,IDSSIM优于比较模型,可以有效地提高疾病语义相似性的准确性,从而提高IDSSIM-WKNNKN模型的关联预测能力;在案例研究方面,IDSSIM预测的大多数潜在的病情相关的LNCRNA可以通过数据库和文献确认,这意味着IDSSIM可以作为预测LNCRNA功能的有前途的工具,识别潜在的LNCRNA疾病关联和预筛查候选者LNCRNA进行生物实验。 IDSSIM代码,所有实验数据和预测结果都在HTTPS://github.com/cdmb-lab/idssim上在线使用。

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