LDAGSO:通过深度学习技术从图序列和疾病本体预测1ncrna -疾病关联

Norah Saeed Awn, Yiming Li, Baoying Zhao, Min Zeng, Min Li
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引用次数: 0

摘要

最近的研究证实了长链非编码rna (1ncRNAs)在理解疾病机制方面的重要作用。由于验证的1ncRNA与疾病之间关联的数量相对较少,并且先前的计算方法在没有捕获序列和本体信息的重要特征方面性能有限,因此我们开发了LDAGSO,一种新的深度学习框架,用于从1ncRNA序列和疾病本体预测1ncRNA和疾病关联。对于1ncRNA序列,我们基于k-mer技术和de Bruijn图将其转换为图结构,并使用图卷积网络捕获图的高级特征。对于疾病,我们从疾病本体树中提取本体术语路径,并将其作为句子处理,利用BERT (Bidirectional Encoder Representations from Transformers)技术获得其特征表示。最后,将这两种特征输入到一个完全连接的层中,以执行1ncrna与疾病之间的关联预测任务。根据结果,我们的方法提供了最先进的结果时,通过留一交叉验证评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LDAGSO: Predicting 1ncRNA-Disease Associations from Graph Sequences and Disease Ontology via Deep Learning techniques
Recent studies have confirmed the significant effects of long non-coding RNAs (1ncRNAs) in understanding the mechanism of diseases. Because of the relatively small number of validated associations between 1ncRNAs and diseases, and previous computational methods have limited performance without capturing important features of sequences and ontology information, we developed LDAGSO, a novel deep learning framework to predict 1ncRNA and disease associations from 1ncRNA sequences and disease ontology. For 1ncRNA sequences, we converted them into graph structure based on k-mer technique and de Bruijn graph, and captured high-level features of the graph using graph convolutional networks. For diseases, we extracted ontology term paths from the disease ontology tree, and treated them as sentences to obtain their feature representation using Bidirectional Encoder Representations from Transformers (BERT) technique. Finally, these two kinds of features were fed into a fully connected layer to perform the task of association prediction between 1ncRNAs and diseases. According to the results, our approach provides state-of-the-art results when evaluated by leave-one-out cross-validation.
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