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Graph Convolutional Network and Convolutional Neural Network Based Method for Predicting lncRNA-Disease Associations

机译:基于图卷积网络和卷积神经网络的lncRNA-疾病关联预测方法

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摘要

Aberrant expressions of long non-coding RNAs (lncRNAs) are often associated with diseases and identification of disease-related lncRNAs is helpful for elucidating complex pathogenesis. Recent methods for predicting associations between lncRNAs and diseases integrate their pertinent heterogeneous data. However, they failed to deeply integrate topological information of heterogeneous network comprising lncRNAs, diseases, and miRNAs. We proposed a novel method based on the graph convolutional network and convolutional neural network, referred to as GCNLDA, to infer disease-related lncRNA candidates. The heterogeneous network containing the lncRNA, disease, and miRNA nodes, is constructed firstly. The embedding matrix of a lncRNA-disease node pair was constructed according to various biological premises about lncRNAs, diseases, and miRNAs. A new framework based on a graph convolutional network and a convolutional neural network was developed to learn network and local representations of the lncRNA-disease pair. On the left side of the framework, the autoencoder based on graph convolution deeply integrated topological information within the heterogeneous lncRNA-disease-miRNA network. Moreover, as different node features have discriminative contributions to the association prediction, an attention mechanism at node feature level is constructed. The left side learnt the network representation of the lncRNA-disease pair. The convolutional neural networks on the right side of the framework learnt the local representation of the lncRNA-disease pair by focusing on the similarities, associations, and interactions that are only related to the pair. Compared to several state-of-the-art prediction methods, GCNLDA had superior performance. Case studies on stomach cancer, osteosarcoma, and lung cancer confirmed that GCNLDA effectively discovers the potential lncRNA-disease associations.
机译:长的非编码RNA(lncRNA)的异常表达通常与疾病相关,疾病相关lncRNA的鉴定有助于阐明复杂的发病机理。预测lncRNA与疾病之间关联的最新方法整合了其相关的异质数据。但是,他们未能深入整合包含lncRNA,疾病和miRNA的异构网络的拓扑信息。我们提出了一种基于图卷积网络和卷积神经网络的新方法,称为GCNLDA,以推断与疾病相关的lncRNA候选物。首先构建包含lncRNA,疾病和miRNA节点的异构网络。根据有关lncRNA,疾病和miRNA的各种生物学前提,构建了lncRNA疾病节点对的嵌入矩阵。开发了基于图卷积网络和卷积神经网络的新框架,以学习lncRNA-疾病对的网络和局部表示。在框架的左侧,基于图卷积的自动编码器将异构lncRNA-疾病-miRNA网络中的拓扑信息深度集成。此外,由于不同的节点特征对关联预测具有歧视性贡献,因此构建了节点特征级别的关注机制。左侧了解了lncRNA-疾病对的网络表示。框架右侧的卷积神经网络通过关注仅与该对相关的相似性,关联性和交互性,学习了lncRNA-疾病对的局部表示。与几种最新的预测方法相比,GCNLDA具有卓越的性能。关于胃癌,骨肉瘤和肺癌的案例研究证实,GCNLDA有效地发现了潜在的lncRNA-疾病关联。

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