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Multimodal Deep Boltzmann Machines for feature selection on gene expression data

机译:多模式Deep Boltzmann机器,用于基因表达数据的特征选择

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In this paper, multimodal Deep Boltzmann Machines (DBM) is employed to learn important genes (biomarkers) on gene expression data from human carcinoma colorectal. The learning process involves gene expression data and several patient phenotypes such as lymph node and distant metastasis occurrence. The proposed framework in this paper uses multimodal DBM to train records with metastasis occurrence. Later, the trained model is tested using records with no metastasis occurrence. After that, Mean Squared Error (MSE) is measured from the reconstructed and the original gene expression data. Genes are ranked based on the MSE value. The first gene has the highest MSE value. After that, k-means clustering is performed using various number of genes. Features that give the highest purity index are considered as the important genes. The important genes obtained from the proposed framework and two sample t-test are being compared. From the accuracy of metastasis classification, the proposed framework gives higher results compared to the top genes from two sample t-test.
机译:在本文中,多模式深部玻尔兹曼机(DBM)用于从人癌大肠的基因表达数据中学习重要的基因(生物标记)。学习过程涉及基因表达数据和几种患者表型,例如淋巴结转移和远处转移。本文提出的框架使用多模式DBM来训练发生转移的记录。之后,使用没有转移发生的记录对训练后的模型进行测试。之后,从重建的和原始的基因表达数据中测量均方误差(MSE)。根据MSE值对基因进行排名。第一个基因具有最高的MSE值。之后,使用多种基因进行k均值聚类。提供最高纯度指数的特征被认为是重要的基因。比较了从提出的框架和两个样本t检验获得的重要基因。从转移分类的准确性来看,与来自两个样本t检验的顶级基因相比,所提出的框架给出了更高的结果。

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