Penalized logistic regression with the adaptive LASSO for gene selection in high-dimensional cancer classification

Lasso(编程语言) 逻辑回归 选择(遗传算法) 估计员 计算机科学 基因选择 弹性网正则化 特征选择 人工智能 回归 支持向量机 机器学习 数据挖掘 统计 数学 微阵列分析技术 基因 生物 遗传学 万维网 基因表达
作者
Zakariya Yahya Algamal,Muhammad Hisyam Lee
出处
期刊:Expert Systems With Applications [Elsevier BV]
卷期号:42 (23): 9326-9332 被引量:118
标识
DOI:10.1016/j.eswa.2015.08.016
摘要

An important application of DNA microarray data is cancer classification. Because of the high-dimensionality problem of microarray data, gene selection approaches are often employed to support the expert systems in diagnostic capability of cancer with high classification accuracy. Penalized logistic regression using the least absolute shrinkage and selection operator (LASSO) is one of the key steps in high-dimensional cancer classification, as gene coefficient estimation and gene selection simultaneously. However, the LASSO has been criticized for being biased in gene selection. The adaptive LASSO (APLR) was originally proposed to overcome the selection bias by assigning a consistent weight to each gene. In high-dimensional data, however, the adaptive LASSO faces practical problems in choosing the type of initial weight. In practice, the LASSO estimator itself has been used as an initial weight. However, this may not be preferable because the LASSO is inconsistent in itself. To address this issue, an alternative initial weight in adaptive penalized logistic regression (CBPLR) is proposed. The effectiveness of the CBPLR is examined on three well-known high-dimensional cancer classification datasets using number of selected genes, area under the curve, and misclassification rate. The experimental results reveal that the proposed CBPLR is quite efficient and feasible for cancer classification. Additionally, the proposed weight is compared with APLR and LASSO and exhibits competitive performance in both classification accuracy and gene selection. The proposed CBPLR has significant impact in penalized logistic regression by selecting fewer genes with high area under the curve and low misclassification rate. Thus, the proposed weight could conceivably be used in other research that implements gene selection in the field of high dimensional cancer classification.
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