There exists unexplained diverse variation within the predefined colon cancer stages using only features either from genomics or histopathological whole slide images as prognostic factors. Unraveling this variation will bring about improved in staging and treatment outcome, hence motivated by the advancement of Deep Neural Network libraries and different structures and factors within some genomic dataset, we aggregate atypical patterns in histopathological images with diverse carcinogenic expression from mRNA, miRNA and DNA Methylation as an integrative input source into an ensemble deep neural network for colon cancer stages classification and samples stratification into low or high risk survival groups. The results of our Ensemble Deep Convolutional Neural Network model show an improved performance in stages classification on the integrated dataset. The fused input features return Area under curve Receiver Operating Characteristic curve (AUC ROC) of 0.95 compared with AUC ROC of 0.71 and 0.68 obtained when only genomics and images features are used for the stage's classification, respectively. Also, the extracted features were used to split the patients into low or high risk survival groups. Among the 2548 fused features, 1695 features showed a statistically significant survival probability differences between the two risk groups defined by the extracted features.
翻译:在预先定义的结肠癌阶段中,存在各种无法解释的差别,仅使用基因组学特征或全细胞病原体图像作为预测性因素,在预定义的结肠癌阶段中,使用基因组学或全细胞病理学图像作为综合输入源,作为结肠癌阶段的混合深神经网络分类和样本分解为低风险或高风险生存组的混合输入源,使用这种变异将改善中转和治疗结果,因此,由于深神经网络图书馆的进步以及某些基因组数据集中不同的结构和因素的推动,因此这种变异将带来更佳的成型和治疗结果,因此,我们结合的输入特征返回曲线收受者操作特征曲线下的0.95区域,与AUC ROC为0.71和0.68的多种致癌表达方式相比,当该阶段的分类仅使用基因组和图像特征将患者分解为低风险或高风险生存组时,我们提取的神经网模型模型显示综合数据集在各阶段的性能特征方面有更好的表现。