ORCID Profile
0000-0001-5839-7504
Current Organisation
Guangxi University
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Publisher: Oxford University Press (OUP)
Date: 12-2022
DOI: 10.1093/BIB/BBAB494
Abstract: Increasing evidences have proved that circRNA plays a significant role in the development of many diseases. In addition, many researches have shown that circRNA can be considered as the potential biomarker for clinical diagnosis and treatment of disease. Some computational methods have been proposed to predict circRNA-disease associations. However, the performance of these methods is limited as the sparsity of low-order interaction information. In this paper, we propose a new computational method (KGANCDA) to predict circRNA-disease associations based on knowledge graph attention network. The circRNA-disease knowledge graphs are constructed by collecting multiple relationship data among circRNA, disease, miRNA and lncRNA. Then, the knowledge graph attention network is designed to obtain embeddings of each entity by distinguishing the importance of information from neighbors. Besides the low-order neighbor information, it can also capture high-order neighbor information from multisource associations, which alleviates the problem of data sparsity. Finally, the multilayer perceptron is applied to predict the affinity score of circRNA-disease associations based on the embeddings of circRNA and disease. The experiment results show that KGANCDA outperforms than other state-of-the-art methods in 5-fold cross validation. Furthermore, the case study demonstrates that KGANCDA is an effective tool to predict potential circRNA-disease associations.
Publisher: Hindawi Limited
Date: 14-09-2021
DOI: 10.1155/2021/6659695
Abstract: circRNA is a novel class of noncoding RNA with closed-loop structure. Increasing biological experiments have shown that circRNAs play an important role in many diseases by acting as a miRNA sponge to indirectly regulate the expression of miRNA target genes. Therefore, predicting associations between circRNAs and miRNAs can promote the understanding of pathogenesis of disease. In this paper, we propose a new computational method, NECMA, based on network embedding to predict potential associations between circRNAs and miRNAs. In our method, the Gaussian interaction profile (GIP) kernel similarities of circRNA and miRNA are calculated based on the known circRNA-miRNA associations, respectively. Then, the circRNA-miRNA association network, circRNA GIP kernel similarity network, and miRNA GIP kernel similarity network are utilized to construct the heterogeneous network. Furthermore, the network embedding algorithm is used to extract potential features of circRNA and miRNA from the heterogeneous network, respectively. Finally, the associations between circRNAs and miRNAs are predicted by using neighborhood regularization logic matrix decomposition and inner product. The performance of NECMA is evaluated by using ten-fold cross-validation. The results show that this method has better prediction accuracy than other state-of-the-art methods.
Publisher: Oxford University Press (OUP)
Date: 2023
DOI: 10.1093/BIB/BBAC613
Abstract: Accumulating evidences demonstrate that circular RNA (circRNA) plays an important role in human diseases. Identification of circRNA-disease associations can help for the diagnosis of human diseases, while the traditional method based on biological experiments is time-consuming. In order to address the limitation, a series of computational methods have been proposed in recent years. However, few works have summarized these methods or compared the performance of them. In this paper, we ided the existing methods into three categories: information propagation, traditional machine learning and deep learning. Then, the baseline methods in each category are introduced in detail. Further, 5 different datasets are collected, and 14 representative methods of each category are selected and compared in the 5-fold, 10-fold cross-validation and the de novo experiment. In order to further evaluate the effectiveness of these methods, six common cancers are selected to compare the number of correctly identified circRNA-disease associations in the top-10, top-20, top-50, top-100 and top-200. In addition, according to the results, the observation about the robustness and the character of these methods are concluded. Finally, the future directions and challenges are discussed.
No related grants have been discovered for Wei Lan.