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Combining High Speed ELM with a CNN Feature Encoding to Predict LncRNA-Disease Associations

机译:将高速ELM与CNN功能组合以预测LncRNA-疾病关联

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Accumulated evidence indicates that IncRNAs are critical for many biological processes, especially diseases. Therefore, identifying potential IncRNA-disease associations is significant for disease prevention, diagnosis, treatment and understanding of cell life activities at the molecular level. Although novel technologies have generated considerable associations for various IncRNAs and diseases, it has inevitable drawbacks such as high cost, time consumption, and error rate. For this reason, integrating various biological databases to predict the potential association of IncRNA and disease is of great attraction. In this paper, we proposed the model called ECLDA to predict IncRNA-disease associations by combining CNN and highspeed ELM. Firstly, the feature vectors are constructed by integrating IncRNA functional similarity, disease semantic similarity and Gaussian interaction profile kernel similarity. Secondly, CNN is carried out to mine local and higher-level abstract features of the vectors. Finally, high speed ELM is used to identify the novel IncRNA disease associations. The ECLDA computational model achieved AUCs of 0.9014 in 5-fold cross validation. The results showed that ECLDA is expected to be a practical tool for biomedical research in the future.
机译:积累的证据表明,IncRNA对许多生物过程,尤其是疾病至关重要。因此,鉴定潜在的IncRNA-疾病关联对于在分子水平上预防疾病,诊断,治疗和理解细胞生命活动具有重要意义。尽管新技术已经为各种IncRNA和疾病产生了可观的关联,但它具有不可避免的缺点,例如高成本,耗时和错误率高。因此,整合各种生物学数据库以预测IncRNA与疾病的潜在关联非常具有吸引力。在本文中,我们提出了一种称为ECLDA的模型,通过结合CNN和高速ELM来预测IncRNA-疾病关联。首先,通过整合IncRNA功能相似性,疾病语义相似性和高斯相互作用谱内核相似性来构建特征向量。其次,进行CNN挖掘矢量的局部和高层抽象特征。最后,高速ELM用于鉴定新的IncRNA疾病关联。 ECLDA计算模型在5倍交叉验证中实现了0.9014的AUC。结果表明,预期ECLDA将成为未来生物医学研究的实用工具。

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