序列对角线性判别分析(SeqDLDA)用于微阵列分类和基因鉴定

R. Pique-Regi, Antonio Ortega, S. Asgharzadeh
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引用次数: 21

摘要

在微阵列分类中,我们面临着大量的特征和很少的训练样本。这对经典的线性判别分析(LDA)来说是一个挑战,因为协方差矩阵无法得到可靠的估计。人们提出了基于对角LDA (DLDA)和独立基因选择(过滤)的替代技术。本文提出了一种结合基因选择和分类的序列DLDA (SeqDLDA)技术。在每次迭代中,依次添加一个基因,并使用DLDA模型(即对角协方差矩阵)重新计算线性判别式(LD)。经典的DLDA将添加t检验分数最高的基因,而不检查结果模型。相比之下,SeqDLDA将在重新计算使用稳健t检验分数测量的模型后找到一个更好地改善类分离的基因。我们在几个2类数据集(神经母细胞瘤、前列腺癌、白血病、结肠癌)中使用10倍交叉验证来评估新方法。例如,对于神经母细胞瘤数据集,使用SeqDLDA将DLDA的平均误分类率(16.91%)显著降低至13.87%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sequential diagonal linear discriminant analysis (SeqDLDA) for microarray classification and gene identification
In microarray classification we are faced with a very large number of features and very few training samples. This is a challenge for classical Linear Discriminant Analysis (LDA), since reliable estimates of the covariance matrix cannot be obtained. Alternative techniques based on Diagonal LDA (DLDA) combined with an independent gene selection (filtering) have been proposed. In this paper we propose a novel sequential DLDA (SeqDLDA) technique that combines gene selection and classification. At each iteration, one gene is sequentially added and the linear discriminant (LD) recomputed using the DLDA model (i.e., a diagonal co-variance matrix). Classical DLDA will add the gene with highest t-test score without checking the resulting model. In contrast, SeqDLDA will find the one gene that better improves class separation after recomputing the model measured using a robustified t-test score. We evaluate the new method in several 2-class datasets (Neuroblastoma, Prostate, Leukemia, Colon) using 10-fold cross-validation. For example, for the Neuroblastoma data set, the average misclassification rate of DLDA (16.91%) is significantly reduced to 13.87% using SeqDLDA.
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