微阵列数据探针选择与分类的人工神经网络与排序方法

Alisson Marques da Silva, A. Faria, Thiago de Souza Rodrigues, Marcelo Azevedo Costa, A. de Pádua Braga
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引用次数: 2

摘要

急性白血病分为髓系和淋巴母细胞亚型通常是根据肿瘤的形态表现来完成的。然而,来自两种亚型的细胞可能具有相似的组织病理学外观,这使得筛选程序非常困难。在疾病的初始阶段对患者进行正确的分类将使医生能够正确地开出癌症治疗处方。因此,为了提高分类率和治疗,需要开发替代方法,以取代通常的形态学分类。本文基于从肿瘤中提取的DNA微阵列数据包含足够的信息来区分白血病亚型的原理。分类任务被描述为一般模式识别问题,需要通过因果定量特征初始表示,然后构建分类器。为了证明我们方法的有效性,我们使用了一个公开的急性白血病数据集,其中包括72个样本和7129个特征。数据集被分成两个子集:训练数据集有38个样本,测试数据集有34个样本。将特征选择方法应用于训练数据集。根据每种方法选出了50个最具预测性的基因。开发了人工神经网络分类器来比较特征选择方法。在使用最佳分类器选择的50个基因中,有21个与之前的工作一致,另有4个与肿瘤分子过程明确相关。剩下的25个被选中的基因能够使用人工神经网络对测试数据集进行正确的分类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial Neural Networks and Ranking Approach for Probe Selection and Classification of Microarray Data
Acute leukemia classification into its Myeloid and Lymphoblastic subtypes is usually accomplished according to the morphological appearance of the tumor. Nevertheless, cells from the two subtypes can have similar histopathological appearance, which makes screening procedures very difficult. Correct classification of patients in the initial phases of the disease would allow doctors to properly prescribe cancer treatment. Therefore, the development of alternative methods, to the usual morphological classification, is needed in order to improve classification rates and treatment. This paper is based on the principle that DNA microarray data extracted from tumors contain sufficient information to differentiate leukemia subtypes. The classification task is described as a general pattern recognition problem, requiring initial representation by causal quantitative features, followed by the construction of a classifier. In order to show the validity of our methods, a publicly available dataset of acute leukemia comprising 72 samples with 7,129 features was used. The dataset was split into two subsets: the training dataset with 38 samples and the test dataset with 34 samples. Feature selection methods were applied to the training dataset. The 50 most predictive genes, according to each method, were selected. Artificial Neural Network (ANN) classifiers were developed to compare the feature selection methods. Among the 50 genes selected using the best classifier, 21 are consistent with previous work and 4 additional ones are clearly related to tumor molecular processes. The remaining 25 selected genes were able to classify the test dataset, correctly, using the ANN.
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