Open Access
Sparse logistic regression with a L1/2 penalty for gene selection in cancer classification
Тип публикации: Journal Article
Дата публикации: 2013-06-19
scimago Q1
wos Q1
БС1
SJR: 1.19
CiteScore: 6.8
Impact factor: 3.3
ISSN: 14712105
PubMed ID:
23777239
Biochemistry
Computer Science Applications
Molecular Biology
Structural Biology
Applied Mathematics
Краткое описание
Microarray technology is widely used in cancer diagnosis. Successfully identifying gene biomarkers will significantly help to classify different cancer types and improve the prediction accuracy. The regularization approach is one of the effective methods for gene selection in microarray data, which generally contain a large number of genes and have a small number of samples. In recent years, various approaches have been developed for gene selection of microarray data. Generally, they are divided into three categories: filter, wrapper and embedded methods. Regularization methods are an important embedded technique and perform both continuous shrinkage and automatic gene selection simultaneously. Recently, there is growing interest in applying the regularization techniques in gene selection. The popular regularization technique is Lasso (L1), and many L1 type regularization terms have been proposed in the recent years. Theoretically, the Lq type regularization with the lower value of q would lead to better solutions with more sparsity. Moreover, the L1/2 regularization can be taken as a representative of Lq (0 < q < 1) regularizations and has been demonstrated many attractive properties. In this work, we investigate a sparse logistic regression with the L1/2 penalty for gene selection in cancer classification problems, and propose a coordinate descent algorithm with a new univariate half thresholding operator to solve the L1/2 penalized logistic regression. Experimental results on artificial and microarray data demonstrate the effectiveness of our proposed approach compared with other regularization methods. Especially, for 4 publicly available gene expression datasets, the L1/2 regularization method achieved its success using only about 2 to 14 predictors (genes), compared to about 6 to 38 genes for ordinary L1 and elastic net regularization approaches. From our evaluations, it is clear that the sparse logistic regression with the L1/2 penalty achieves higher classification accuracy than those of ordinary L1 and elastic net regularization approaches, while fewer but informative genes are selected. This is an important consideration for screening and diagnostic applications, where the goal is often to develop an accurate test using as few features as possible in order to control cost. Therefore, the sparse logistic regression with the L1/2 penalty is effective technique for gene selection in real classification problems.
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ГОСТ
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Liang Y. et al. Sparse logistic regression with a L1/2 penalty for gene selection in cancer classification // BMC Bioinformatics. 2013. Vol. 14. No. 1. 198
ГОСТ со всеми авторами (до 50)
Скопировать
Liang Y., Liu C., Luan X. Z., LEUNG K., Chan T., Xu Z. B., Zhang H. Sparse logistic regression with a L1/2 penalty for gene selection in cancer classification // BMC Bioinformatics. 2013. Vol. 14. No. 1. 198
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TY - JOUR
DO - 10.1186/1471-2105-14-198
UR - https://doi.org/10.1186/1471-2105-14-198
TI - Sparse logistic regression with a L1/2 penalty for gene selection in cancer classification
T2 - BMC Bioinformatics
AU - Liang, Yong
AU - Liu, Cheng
AU - Luan, Xin Ze
AU - LEUNG, KWONG-SAK
AU - Chan, Tak-Ming
AU - Xu, Zong Ben
AU - Zhang, Hai
PY - 2013
DA - 2013/06/19
PB - Springer Nature
IS - 1
VL - 14
PMID - 23777239
SN - 1471-2105
ER -
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@article{2013_Liang,
author = {Yong Liang and Cheng Liu and Xin Ze Luan and KWONG-SAK LEUNG and Tak-Ming Chan and Zong Ben Xu and Hai Zhang},
title = {Sparse logistic regression with a L1/2 penalty for gene selection in cancer classification},
journal = {BMC Bioinformatics},
year = {2013},
volume = {14},
publisher = {Springer Nature},
month = {jun},
url = {https://doi.org/10.1186/1471-2105-14-198},
number = {1},
pages = {198},
doi = {10.1186/1471-2105-14-198}
}