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Novel hybrid DCNN–SVM model for classifying RNA-sequencing gene expression data

机译:用于分类RNA测序基因表达数据的新型混合DCNN–SVM模型

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ABSTRACT In recent years, cancer is one of the leading causes of death worldwide. Therefore, there are more and more studies that have been conducted to find effective solutions to diagnose and treat cancer. However, there are still many challenges in cancer treatment because possible causes of cancer are genetic disorders or epigenetic alterations in the cells. RNA sequencing is a powerful technique for gene expression profiling in model organisms and it is able to produce information for diagnosing cancer at the biomolecular level. Gene expression data are used to build a classification model which supports treatment of cancer. Nevertheless, its characteristic is very-high-dimensional data which lead to over-fitting issue of classifying model. In this paper, we propose a new gene expression classification model of support vector machines (SVM) using features extracted by deep convolutional neural network (DCNN). In our approach, the DCNN extracts latent features from gene expression data, then they are used in conjunction with SVM that efficiently classify RNA-Seq gene expression data. Numerical test results on RNA-Seq gene expression datasets from The Cancer Genome Atlas (TCGA) illustrate that our proposed algorithm is more accurate than state-of-the-art classifying models including DCNN, SVM and random forests.
机译:摘要近年来,癌症是世界范围内主要的死亡原因之一。因此,进行了越来越多的研究以找到诊断和治疗癌症的有效解决方案。然而,在癌症治疗中仍然存在许多挑战,因为癌症的可能原因是遗传异常或细胞中的表观遗传学改变。 RNA测序是一种在模型生物中进行基因表达谱分析的有力技术,它能够为生物分子水平的癌症诊断提供信息。基因表达数据用于建立支持癌症治疗的分类模型。然而,它的特征是非常高维的数据,这导致分类模型的过拟合问题。在本文中,我们利用深度卷积神经网络(DCNN)提取的特征,提出了一种新的支持向量机(SVM)的基因表达分类模型。在我们的方法中,DCNN从基因表达数据中提取潜在特征,然后将它们与SVM结合使用,从而有效地对RNA-Seq基因表达数据进行分类。来自癌症基因组图谱(TCGA)的RNA-Seq基因表达数据集的数值测试结果表明,我们提出的算法比包括DCNN,SVM和随机森林在内的最新分类模型更为准确。

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