机制(生物学)
超图
水准点(测量)
计算机科学
鉴定(生物学)
特征(语言学)
卷积神经网络
相似性(几何)
机器学习
构造(python库)
人工智能
计算生物学
理论计算机科学
邻接表
特征学习
数据挖掘
计算模型
模棱两可
产品(数学)
数据集成
原始数据
生物学数据
公制(单位)
深度学习
基础(线性代数)
人工神经网络
方案(数学)
模式识别(心理学)
特征提取
关系数据库
语义学(计算机科学)
理性
数据建模
作者
Lei Chen,Ying Chen,Bo Zhou
标识
DOI:10.1021/acs.jcim.5c01968
摘要
Circular RNA (circRNA)-microRNA (miRNA) interactions (CMIs) play important roles in regulating gene expression, cell proliferation, and tumorigenesis. Accurate identification of CMIs is critical for understanding disease pathogenesis and for advancing diagnostic and therapeutic strategies. However, conventional biological experiments are time-consuming and labor-intensive, and existing computational models, although effective, still provide suboptimal circRNA and miRNA representations. Here, we propose HCLAMCMI, a computational model for the CMI prediction. Three types of raw features of circRNAs and miRNAs were extracted from the adjacency matrix, similarity matrix, and heterogeneous network comprising circRNAs, miRNAs, and diseases. Hypergraphs were then constructed from two complementary views to capture high-order relational information. These hypergraphs were processed by using hypergraph convolutional networks, contrastive learning, and a channel attention mechanism to generate high-level feature representations. The features were subsequently refined through two-layer fully connected neural networks, and interaction scores were obtained by the inner product to construct the recommendation matrix. HCLAMCMI was evaluated on two benchmark CMI data sets, achieving AUC and AUPR values above 0.98 on training data sets and approximately 0.97 on independent test data sets, consistently outperforming all existing models. Additional analyses confirmed the rationality of its architecture and highlighted the advantages of integrating hypergraph-based learning with attention mechanisms.
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