Development of Machine Learning based Colorectal Cancer Subtype Classificator*

Fruzsina Kulcsár, Dániel Békevári, G. Eigner, D. Drexler, Á. Patai, T. Micsik, Rita Fleiner
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Abstract

The 4 Consensus Molecular Subtypes (CMS1-4) determined by the Colorectal Cancer subtyping Consortium (CRCSC) could have been identified by high-priced methods so far. This study aimed at building a model which can reliably classify patients into the same subtypes with high accuracy using data from publicly available datasets and less expensive clinical procedures. The gene expression data from The Cancer Genome Atlas (TCGA) database was used as a basis for classifying the patients. Our objective was to decrease the number of considered genes from 20000 to around 100 without significant deterioration of the predictive ability of the model. In order to perform the classification, Artificial Neural Networks were trained for the labeled data of the total number of dimensions checking the goodness of the patient classification. Then dimensionality reduction was used, paying attention not to decrease the integrity of the classification significantly. We managed to reduce the number of genes to 100, while we did not deteriorate the accuracy of the classification drastically. The final model on the reduced geneset produced a result of 82% accuracy. The developed software can be used for classifying patients with colorectal cancer. The 100 genes have to be provided for each patient, and the software returns 4 probabilities as a result: the probabilities of belonging to either of the 4 subtypes. The subtype with the highest probability is the final result of the classification.
基于机器学习的结直肠癌亚型分类器的开发*
迄今为止,结直肠癌亚型联盟(CRCSC)确定的4种共识分子亚型(CMS1-4)可以通过高价方法进行鉴定。本研究旨在建立一个模型,该模型可以使用来自公开数据集的数据和更便宜的临床程序,以高精度可靠地将患者分为相同的亚型。肿瘤基因组图谱(The Cancer Genome Atlas, TCGA)数据库中的基因表达数据作为患者分类的依据。我们的目标是将考虑的基因数量从20000个减少到100个左右,同时不显著降低模型的预测能力。为了进行分类,对总维数的标记数据进行人工神经网络训练,检验患者分类的优良性。然后采用降维方法,注意不显著降低分类的完整性。我们设法将基因数量减少到100个,而我们并没有大幅降低分类的准确性。在简化的基因集上的最终模型产生了82%的准确率。所开发的软件可用于结直肠癌患者的分类。必须为每个患者提供100个基因,然后软件返回4种概率:属于4种亚型中的任何一种的概率。概率最高的子类型是分类的最终结果。
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