Abstract
Background
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 (L_{1}), and many L_{1} 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 L_{1/2} regularization can be taken as a representative of Lq (0 < q < 1) regularizations and has been demonstrated many attractive properties.
Results
In this work, we investigate a sparse logistic regression with the L_{1/2} penalty for gene selection in cancer classification problems, and propose a coordinate descent algorithm with a new univariate half thresholding operator to solve the L_{1/2} 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 L_{1/2} regularization method achieved its success using only about 2 to 14 predictors (genes), compared to about 6 to 38 genes for ordinary L_{1} and elastic net regularization approaches.
Conclusions
From our evaluations, it is clear that the sparse logistic regression with the L_{1/2} penalty achieves higher classification accuracy than those of ordinary L_{1} 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 L_{1/2} penalty is effective technique for gene selection in real classification problems.
Keywords:
Gene selection; Sparse logistic regression; Cancer classificationBackground
With the development of DNA microarray technology, the biology researchers can analyze the expression levels of thousands of genes simultaneously. Many studies have demonstrated that microarray data are useful for classification of many cancers. However, from the biological perspective, only a small subset of genes is strongly indicative of a targeted disease, and most genes are irrelevant to cancer classification. The irrelevant genes may introduce noise and decrease classification accuracy. Moreover, from the machine learning perspective, too many genes may lead to overfitting and can negatively influence the classification performance. Due to the significance of these problems, effective gene selection methods are desirable to help to classify different cancer types and improve prediction accuracy.
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. Filter methods evaluate a gene based on discriminative power without considering its correlations with other genes [14]. The drawback of filter methods is that it examines each gene independently, ignoring the possibility that groups of genes may have a combined effect which is not necessarily reflected by the individual performance of genes in the group. This is a common issue with statistical methods such as Ttest, which examine each gene in isolation.
Wrapper methods utilize a particular learning method as feature evaluation measurement to select the gene subsets in terms of the estimated classification errors and build the final classifier. Wrapper approaches can obtain a small subset of relevant genes and can significantly improve classification accuracy [5,6]. For example, Guyon et al. [7] proposed a gene selection approach utilizing support vector machines (SVM) based on recursive feature elimination. However, the wrapper methods greatly require extensive computational time.
The third group of gene selection procedures is embedded methods, which perform the variable selection as part of the statistical learning procedure. They are much more efficient computationally than wrapper methods with similar performance. Embedded methods have drawn much attention recently in the literature. The embedded methods are less computationally expensive and less prone to over fitting than the wrapper methods [8].
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 the logistic regression models. Logistic regression is a powerful discriminative method and has a direct probabilistic interpretation which can obtain probabilities of classification apart from the class label information. In order to extract key features in classification problems, a series of regularized logistic regression methods have been proposed. For example, Shevade and Keerthi [9] proposed the sparse logistic regression based on the Lasso regularization [10] and GaussSeidel methods. Glmnet is the general approach for the L_{1} type regularized (including Lasso and elastic net) linear model using a coordinate descent algorithm [11,12]. Similar to sparse logistic regression with the L_{1} regularization method, Gavin C. C. and Nicola L. C. [13] investigated sparse logistic regression with Bayesian regularization. Inspired by the aforementioned methods, we investigate the sparse logistic regression model with a L_{1/2} penalty, in particular for gene selection in cancer classification. The L_{1/2} penalty can be taken as a representative of Lq (0 < q < 1) penalty and has demonstrated many attractive properties, such as unbiasedness, sparsity and oracle properties [14].
In this paper, we develop a coordinate descent algorithm to the L_{1/2} regularization in the sparse logistic regression framework. The approach is applicable to biological data with high dimensions and low sample sizes. Empirical comparisons with sparse logistic regressions with the L_{1} penalty and the elastic net penalty demonstrate the effectiveness of the proposed L_{1/2} penalized logistic regression for gene selection in cancer classification problems.
Methods
Sparse logistic regression with the L_{1/2} penalty
In this paper, we focus on a general binary classification problem. Suppose we have n samples, D = {(X_{1}, y_{1}), (X_{2}, y_{2}), …, (X_{n}, y_{n})}, where X_{i} = (x_{i1}, x_{i2} , …, x_{ip}) is i^{th} input pattern with dimensionality p and y_{i} is a corresponding variable that takes a value of 0 or 1; y_{i}= 0 indicates the i^{th} sample in Class 1 and y_{i}= 1 indicates the i^{th} sample is in Class 2. The vector X_{i} contains p features (for all p genes) for the i^{th} sample and x_{ij} denotes the value of gene j for the i^{th} sample. Define a classifier f(x) = e^{x} /(1 + e^{x}) such that for any input x with class label y, f(x) predicts y correctly. The logistic regression is expressed as:
Where β = (β_{0}, β_{1},…, β_{p}) are the coefficients to be estimated, note that β_{0} is the intercept. The loglikelihood is:
We can obtain β by minimizing the loglikelihood (2). In high dimensional application with p >> n, directly solving the logistic model (2) is illposed and may lead to overfitting. Therefore, the regularization approaches are applied to address the overfitting problem. When adding a regularization term to (2), the sparse logistic regression can be modelled as:
Where λ > 0 is a tuning parameter and P(B) is a regularization term. The popular regularization technique is Lasso (L_{1}) [10], which has the regularization term P(β) = ∑ β. Many L_{1} type regularization terms have been proposed in the recent years, such as SCAD [15], elastic net [16], and MC+ [17].
Theoretically, the Lq type regularization P(β) = ∑ β^{q} with the lower value of q would lead to better solutions with more sparsity. However when q is very close to zero, difficulties with convergence arise. Therefore, Xu et al. [14] further explored the properties of Lq (0 <q <1) regularization and revealed the extreme importance and special role of the L_{1/2} regularization. They proposed that when 1/2< q <1, the L_{1/2} regularization can yield most sparse results and its difficulty with convergence is not very high compared with that of the L_{1} regularization, while when 0< q <1/2, the performance of Lq penalties makes no significant difference and solving the L_{1/2} regularization is much simpler than solving the L_{0} regularization. Hence, the L_{1/2} regularization can be taken as a representative of Lq (0 < q < 1) regularizations. In this paper, we apply the L_{1/2} penalty to the logistic regression model. The sparse logistic regression model based on the L_{1/2} penalty has the form:
The L_{1/2} regularization has been demonstrated many attractive properties, such as unbiasedness, sparsity and oracle properties. The theoretical and experimental analyses show that the L_{1/2} regularization is a competitive approach. Our work in this paper also reveals the effectiveness of the L_{1/2} regularization to solve the nonlinear logistic regression problems with a small number of predictive features (genes).
A coordinate descent algorithm for the L_{1/2} penalized logistic regression
The coordinate descent algorithm [11,12] is a “oneatatime” approach, and its basic procedure can be described as follows: for each coefficients, to partially optimize the target function with respect to β_{j}(j = 1, 2, …, p) with the remaining elements of β fixed at their most recently updated values.
Before introducing the coordinate descent algorithm for the nonlinear logistic regularization, we first consider a linear regularization case. Suppose the dataset D has n samples, D = {(X_{1}, y_{1}), (X_{2}, y_{2}), …, (Xn, y_{n})}, where X_{i} = (x_{i1}, x_{i2}, …, x_{ip}) is i^{th} input variables with dimensionality p and y_{i} is the corresponding response variable. The variables are standardized: and Therefore, The linear regression with the regularization term can be expressed as:
Where P(B) is the regularization term. The coordinate descent algorithm solves β_{j} and other β_{k ≠ j} (k ≠ j represent the parameters remained after j^{th} element is removed) are fixed. The equation (5) can be rewritten as:
The first order derivative at β_{j} can be estimated as:
Define as the partial residual for fitting β_{j} and , the univariate soft thresholding operator of the coordinate descent algorithm [11] for the L_{1} regularization (Lasso) can be defined as:
Similarly, for the L_{0} regularization, the thresholding operator of the coordinate descent algorithm can be defined as:
where I is the indicator function. This formula is equivalent to the hard thresholding operator [17].
According to equations (8) and (9), we can know that the different penalties are associated with different thresholding operators. Therefore, Xu et al. [18] proposed a half thresholding operator to solve the L_{1/2} regularization for linear regression model. It is an iterative algorithm and can be seen as multivariate half thresholding approach. In this paper, we propose the univariate half thresholding operator of the coordinate descent algorithm for the L_{1/2} regularization. Based on equation (7), the gradient of the L_{1/2} regularization at β_{j} can be expressed as:
Firstly, we consider the β_{j} > 0 statement, and let, , β_{j} = μ^{2}. When β_{j} > 0, the equation (10) can be redefined as:
There are three cases of ω_{j} < 0, , and respectively.
(i) If ω_{j} < 0, the three roots of equation (11) can be expressed as follows: andwhere , . When r > 0, none of the roots satisfices μ_{1} > 0. Thus, there is no solution to equation (11) when ω_{j} < 0.
(ii) If , the three roots of equation (11) are:
There is still no solution to equation (11) in this case.
(iii) If , the three roots of equation (11) are given by:
In this case, the μ_{2} is a unique solution of equation (10). Thus, the equation (11) has nonzero roots only when . The unique solution of equation (10) is as follow:
On the other hand, in the β_{j} < 0 statement, we denoted and β_{j} =  μ^{2}. The equation (10) can be transformed into the equation:
The equation (12) also has a unique solution when :
In conclusion, the univariate half thresholding operator can be expressed as:
where φ_{λ}(ω) satisfies:
The coordinate descent algorithm for the L_{1/2} regularization makes repeated use of the univariate half thresholding operator. The details of the algorithm will be described later. This coordinate descent algorithm for the regularization can be extended to the sparse logistic regression model. Based on the objective function (3) of the sparse logistic regression, oneterm Taylor series expansion for l(B) has the form of
Where is an estimated response, is a weight and is a evaluated value at current parameters. Redefine the partial residual for fitting current as and , we can directly apply the coordinate descent algorithm with the L_{1/2} penalty for sparse logistic regression and the details are given follows:
Algorithm: The coordinate descent algorithm for sparse logistic with the L_{1/2} penalty
The coordinate descent algorithm for the L_{1/2} penalized logistic regression works well in the sparsity problems, because the procedure does not need to change many irrelevant parameters and recalculate partial residuals for each update step.
Results
Analyses of simulated data
In this section, we evaluate the performance of the sparse logistic regression with the L_{1/2} penalty in simulation study. We generate highdimensional and low sample size data which contain many irrelevant features. Two methods are compared with our proposed approach: Sparse logistic regression with the Elastic Net penalty (L_{EN}) and Sparse logistic regression with the Lasso penalty (L_{1}).
We generated the vectors γ_{i0},γ_{i1},…,γ_{ip} (i = 1,…,n) independently from the standard normal distribution and the predictor vector(i=1,…,n) is generated by (j=1,…, p), where ρ is the correlation coefficient of the predictor vectors [19]. The simulated data set generated from the logistic model:
Where ϵ is the independent random error generated from N(0,1) and σ is the parameter which controls the signal to noise. In every simulation, the dimension p of the predictor vector is 1000, and the first five true coefficients are nonzero: β_{1} = 1, β_{2} = 1, β_{3} = 1, β_{4} = 1, β_{5} = 1, and β_{j} = 0(6 ≤ j ≤ 1000).
The estimation of the optimal tuning parameter λ in the sparse logistic regression models can be done in many ways and is often done by kfold crossvalidation (CV). Note that the choice of k will depend on the size of the training set. In our experiments, we use 10fold crossvalidation (k=10). The elastic net method has two tuning parameters, we need to crossvalidate on a twodimensional surface [16].
We consider the cases with the training sample size n = 50, 80, 100, the correlation coefficient ρ =0.1, 0.4 and the noise control parameter σ =0.2, 0.6 respectively. Each classifier was evaluated on a test data set including 100 samples. The experiments were repeated 30 times and we report the average test errors in Table 1. As shown in Table 1, when the sample size n increases, the prediction performances of all the three methods are improved. For example when ρ =0.1, and σ =0.2, the average test errors of the L_{1/2} method are 28.2%, 10.7% and 8.1% with the sample sizes n=50, 80, and 100 respectively. When the correlation parameter ρ and the noise parameter σ increase, the prediction performances of all the three methods are decreased. For example, when ρ =0.4 and n =100, the average test errors from the L_{1/2} method increased from 9.1% to 15.1%, in which σ increased from 0.2 to 0.6. When σ =0.6 and n =80, the average test error from the L_{1/2} method increase from 18.4% to 20.5%, in which ρ increased from 0.1 to 0.4. Moreover, in our simulation, the influence of the noise may be larger than that of the variable correlation for the prediction performance of all the three methods. On the other hand, at the same parameter setting case, the prediction performance of the L_{1/2} method is consistent and better than the results of the L_{EN} and L_{1} methods. For example, whenρ =0.1, σ =0.2 and n=100, the predictive error of the L_{1/2} method is 8.1% much better than 16.9% and 15.7% got by the L_{EN} and L_{1} methods respectively.
Table 1. The average errors (%) for the test data sets obtained by the sparse logistic regressions with the L_{1/2}, L_{EN }and L_{1 }penalties in 30 runs
Table 2 shows the average number of the variables selected in 30 runs for each method. Since the simulation datasets have x_{1}x_{5} relevant features, the idealized average number of variables selected by each method is 5. In Table 2, the results obtained by the L_{1/2} penalized method are obviously closed to 5 and 3–10 times smaller than those of the L_{EN} and L_{1} penalties at the same parameter setting. For example, when ρ =0.1, σ =0.2 and n=100, the average numbers from the L_{EN} and L_{1} methods are 49.7 and 45.7 respectively, and the result of L_{1/2} method is 8.9. Moreover, when the sample size n, the correlation parameter ρ, and the noise parameter σ increase, the average numbers from all the three methods increase, but the values of the L_{EN} and L_{1} methods increase faster than those of the L_{1/2} method. This means that the L_{1/2} penalized method consistently outperforms than other two methods in term of variable selection.
Table 2. The average number of variables selected by the sparse logistic regressions with the L_{1/2}, L_{EN }and L_{1 }penalties in 30 runs
To further evaluate the performance of the L_{1/2} penalized method, we report the frequency with which each relevant variable was selected among 30 runs for each method in Table 3. When the sample size is small (n=50), the L_{1/2} penalty selects the relevant variables slightly less frequently than the other two methods and all the three methods select true nonzero coefficients with difficulties, especially when ρ and σ are relatively large. For example, when ρ =0.4, σ =0.6, n=50, and for β_{5}, the selected frequencies of the L_{1/2}, L_{EN} and L_{1} methods are 12, 14 and 13 respectively in 30 runs. As n increases, all the three methods tend to select the true nonzero coefficients more accurately and the L_{1/2} penalty method performs slightly better, in terms of variable frequencies, than the other two methods under the different parameter settings of ρ and σ. To sum up, Tables 1, 2 and 3 clearly show that the L_{1/2} method is winner among the competitors in terms of both prediction accuracy and variable selection in the different variable correlation and noise situations.
Table 3. The frequencies of the relevant variables obtained by the sparse logistic regressions with the L_{1/2}, L_{EN }and L_{1 }penalties in 30 runs
Analyses on microarray data
In this section, we compare our proposed L_{1/2} penalized method with the L_{EN} and L_{1} methods on 4 publicly available gene expression datasets: Leukaemia, Prostate, Colon and DLBCL. A brief description of these datasets is given below and summarized in Table 4.
Table 4. Four publicly available gene expression datasets used in the experiments
Leukaemia dataset
The original dataset was provided by Golub et al. [7], and contains the expression profiles of 7,129 genes for 47 patients of acute lymphoblastic leukaemia (ALL) and 25 patients of acute myeloid leukaemia (AML). For data preprocessing, we followed the protocol detailed in the supplementary information to Dudoit et al. [1]. After thresholding, filtering, applying a logarithmic transformation and standardizing each expression profile to zero mean and unit variance, a dataset comprising 3,571 genes remained.
Prostate dataset
This original dataset contains the expression profiles of 12,600 genes for 50 normal tissues and 52 prostate tumor tissues. For data preprocessing, we adopt the pretreatment method [20] to obtain a dataset with 102 samples. And each sample contains 5966 genes.
Colon dataset
The colon microarray data set in Alon et al. [21] has 2000 genes per sample and 62 samples which consist of 22 normal tissues and 40 cancer tissues. The Colon dataset are available at http://microarray.princeton.edu/oncology webcite.
DLBCL dataset
This dataset contains 77 microarray gene expression profiles of the 2 most prevalent adult lymphoid malignancies: 58 samples of diffuse large Bcell lymphomas (DLBCL) and 19 observations of follicular lymphoma (FL). Each sample contains 7,129 gene expression values. More information on these data can be found in Shipp MA et al. [22]. For data preprocessing, we followed the protocol detailed in the supplementary information to Dudoit et al. [1], and a dataset comprising 6,285 genes remained.
We evaluate the prediction accuracy of the three penalized logistic regression models using random partition. This means that we divide the datasets at random such that approximate 7080% of the datasets becomes training samples and the other 2030% test samples. More information on these data is given in Table 5. For selecting the tuning parameter λ, we employ the tenfold cross validation scheme using the training set. We repeat this procedure 30 times and the averaged misclassification errors were reported in Table 6. Here the denominators of the tenfold cross validation errors and the test errors describe the sample size of training and test datasets respectively. The fractions of the tenfold cross validation errors and the test errors and the number of gene selected are the approximated integers of the corresponding average number at 30 runs. As shown in Table 6, for Leukaemia dataset, the classifier with the L_{1/2} penalty gives the average tenfold cross validation error of 2/50 and the average test error of 1/22 with about 2 genes selected. The classifiers with L_{EN} and L_{1} methods give the average tenfold cross validation errors of 1/50 and the average test errors of 1/22 with about 9 and 6 genes selected respectively. This means that all three methods can be successfully applied to highdimensional classification problems and classify the Leukaemia dataset with same accuracies. Note that, the L_{1/2} method achieved its success using only about 2 predictors (genes), compared to about 9 and 6 for the L_{EN} and L_{1} methods. For Prostate and Colon datasets, it can be seen the L_{1/2} method achieves the best classification performances with the highest accuracy rates using much fewer genes compared with those of the L_{EN} and L_{1} methods. For DLBCL dataset, the L_{1/2} logistic regression achieves better classification performance than that of the L_{1} method and worse than that of the L_{EN} method. However, as well as other three datasets, the L_{1/2} method achieved its success using much less predictors (about 14 genes), compared to about 38 and 23 for the L_{EN} and L_{1} methods. 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.
Table 5. The detail information of 4 microarray datasets used in the experiments
Table 6. The classification performances of different methods for 4 gene expression datasets
Figures 1, 2 and 3 display the solution paths and the gene selection results of the three methods for the Prostate dataset in one sample run. Here the xaxis displays the number of running steps, the yaxis in the left subfigure is the coefficients measured gene importance and the yaxis in the right subfigure is the misclassification errors based on the tenfold cross validation. The optimal results of three methods are shown as vertical dotted lines. Figure 1 indicates that the number of nonzero coefficients (selected genes) of the optimal results obtained by the L_{1/2} method is 5. In contrast, Figures 2 and 3 indicate that the numbers of nonzero coefficients (selected genes) of optimal results obtained by the L_{EN} and L_{1} methods are 37 and 26 respectively. Generally speaking, the penalized logistic regression methods can be successfully applied to the cancer classification problems with high dimensional and low samples microarray data, and our proposed L_{1/2} method achieves better performance especially in gene selection.
Figure 1. The results of the sparse logistic regression with the L_{1/2 }penalty on Prostate dataset. The solution paths and the gene selection results of the sparse logistic L_{1/2} penalty methods for the Prostate dataset in one sample run.
Figure 2. The results of the sparse logistic regression with the L_{EN }penalty on Prostate dataset. The solution paths and the gene selection results of the sparse logistic elastic net penalty methods for the Prostate dataset in one sample run.
Figure 3. The results of the sparse logistic regression with the L_{1 }penalty on Prostate dataset. The solution paths and the gene selection results of the sparse logistic L_{1} penalty methods for the Prostate dataset in one sample run.
Brief biological analyses of the selected genes
The summaries of the 10 topranked informative genes found by the three sparse logistic regression methods for 4 gene expression datasets are shown in Tables 7, 8, 9 and 10 respectively. The genes with star(*) are the most frequently selected genes to construct the classifiers according to the last column of Table 6, and the common genes obtained by each classifier are emphasized with bold. The biologically experimental results proved some genes included in the frequently selected gene sets that produce high classification accuracy rate are mostly and functionally related to carcinogenesis or tumor histogenesis. For example, in Table 7, the most frequently selected gene set of each sparse logistic method for leukemia classification, including cystatin C (CST3) and myeloperoxidase (MPO) genes, that achieve high classification accuracy by the L_{1/2} method, are experimentally proved to be correlated to leukemia of ALL or AML. The cystatin C gene is located at the extracellular region of the cell and has role in invasiveness of human glioblastoma cells. Decrease of cystatin C in the CSF might contribute to the process of metastasis and spread of the cancer cells in the leptomeningeal tissues [23]. The myeloperoxidase gene is taking role in antiapoptosis process where cancer cells kill themselves [24]. For the colon dataset (Table 9), the most frequently selected gene set of each sparse logistic method includes genes such as guanylate cyclase activator 2B (GUCA2B), myosin, light chain 6, alkali, smooth muscle and nonmuscle (MYL6) and Human desmin (DES) genes. These genes are the top 3 significant informative genes ranked by our proposed L_{1/2} method and also selected by BenDor et al. [25], Yang and Song [26] and Li et al. [27]. On the top of these genes lists is guanylate cyclase activator 2B (GUCA2B) gene. Notterman et al. [28] showed that a reduction of uroguanylin might be an indication of colon tumors, and Shailubhai et al. [29] reported that treatment with uroguanylin has a positive therapeutic significance to the reduction in precancerous colon ploys.
Table 7. The 10 topranked informative genes found by the three sparse logistic regression methods from the Leukaemia dataset
Table 8. The 10 topranked informative genes found by the three sparse logistic regression methods from the Prostate dataset
Table 9. The 10 topranked informative genes found by the three sparse logistic regression methods from the colon dataset
Table 10. The 10 topranked informative genes found by the three sparse logistic regression methods from the DLBCL dataset
In Tables 7, 8, 9 and 10, some genes are only frequently selected by the L1/2 method, but not discovered by the L_{EN} and L_{1} methods. The evidence from the literatures showed that they are cancer related genes. For example, for the colon dataset, the genes cholinergic receptor, nicotinic, delta polypeptide (CHRND) and platelet/endothelial cell adhesion molecule1 (PECAM1) were also selected by Maglietta R. et al. [30], Wiese A.H. et al. [31], Wang S. L. et al. [32], and Dai J. H. and Xu Q. [33]. These genes can significantly discriminate between nondissected tumors and micro dissected invasive tumor cells. It is remarkable that apparently (to our knowledge) some discovered genes that have not been seen in any past studies.
On the other hand, from Tables 7, 8, 9 and 10, we found that the most frequently selected genes and their ranking orders by the LEN and L1 methods are much similar compared with those of the L1/2 method. The main reasons are that the classification hypothesis needs not be unique as the samples in gene expression data lie in a highdimensional space, and both of the LEN and L1 methods are based on the L1 type penalty.
Construct KNN classifier with the most frequently selected relevant genes
In this section, to further evaluate the performance and prediction generality of the sparse logistic regression with L_{1/2} penalty, we constructed KNN (k =3, 5) classifiers using the relevant genes which were most frequently selected by the L_{1/2} penalized logistic regression method. In this experiment, we use the random leaveoneout cross validation (LOOCV) to evaluate the predictive ability and repeat 50 runs.
Table 11 summarizes classification accuracies of four datasets with KNN classifiers with selected genes by our proposed methods. From Table 11, we can see that all the classification accuracies are high than 90%, especially the classification accuracy on the Leukaemia dataset is 98.3%. The KNN classifiers with relevant genes which were selected by the sparse logistic regression with the L_{1/2} penalty can achieve high classification accuracy. The results indicate that the sparse logistic regression with the L_{1/2} penalty can select power discrimination genes.
Table 11. Summary of the results of KNN classifiers using the most frequently selected genes by our proposed L_{1/2 }penalized logistic regression method
Conclusions
In cancer classification application based on microarray data, only a small subset of genes is strongly indicative of a targeted disease. Thus, feature selection methods play an important role in cancer classification. In this paper, we propose and model sparse logistic regression with the L_{1/2} penalty, and develop the corresponding coordinate descent algorithm as a novel gene selection approach. The proposed method utilizes a novel univariate half thresholding to update the estimated coefficients.
Both simulation and microarray data studies show that the sparse logistic regression with the L_{1/2} penalty achieve higher classification accuracy than those of ordinary L_{1} and elastic net regularization approaches, while fewer but informative genes are selected. Therefore, the sparse logistic regression with the L_{1/2} penalty is the effective technique for gene selection in real classification problem.
In this paper, we use the proposed method to solve binary cancer classification problem. However, many cancer classification problems involve multicategory microarray data. We plan to extend our proposed method to solve multinomial penalized logistic regression for multiclass cancer classification in our future work.
Competing interests
All authors declare they have no competing interests.
Authors’ contributions
YL, CL and XZL developed the gene selection methodology, designed and carried out the comparative study, wrote the code, and drafted the manuscript. KSL, TMC, ZBX and HZ brought up the biological problem that prompted the methodological development and verified and provided discussion on the methodology, and coauthored the manuscript. The authors read and approved the manuscript.
Acknowledgements
This research was supported by Macau Science and Technology Develop Funds (Grant No. 017/2010/A2) of Macau SAR of China and the National Natural Science Foundations of China (Grant No. 2013CB329404, 11131006, 61075054, and 11171272).
References

Dudoit S, Fridlyand S, Speed TP: Comparison of discrimination methods for the classification of tumors using gene expression data.
J Am Stat Assoc 2002, 97(457):7787. Publisher Full Text

Li T, Zhang C, Ogihara M: A comparative study of feature selection and multiclass classification methods for tissue classification based on gene expression.
Bioinformatics 2004, 20:24292437. PubMed Abstract  Publisher Full Text

Lee JW, Lee JB, Park M, Song SH: An extensive evaluation of recent classification tools applied to microarray data.
Com Stat Data Anal 2005, 48:869885. Publisher Full Text

Ding C, Peng H: Minimum redundancy feature selection from microarray gene expression data.
J. Bioinform. Comput 2005, 3(2):185205. Publisher Full Text

Monari G, Dreyfus G: Withdrawing an example from the training set: an analytic estimation of its effect on a nonlinear parameterized model.
Neurocomputing Letters 2000, 35:195201. Publisher Full Text

Rivals I, Personnaz L: MLPs (monolayer polynomials and multilayer perceptrons) for nonlinear modeling.

Golub T, Slonim D, Tamayo P, Huard C, Gaasenbeek M, Mesirov J, Coller H, Loh M, Downing J, Caligiuri M, Bloomfield C, Lander E: Molecular classification of cancer: class discovery and class prediction by gene expression monitoring.
Science 1999, 286:531537. PubMed Abstract  Publisher Full Text

Guyon I, Elisseff A: An Introduction to variable and feature selection.

Shevade SK, Keerthi SS: A simple and efficient algorithm for gene selection using sparse logistic regression.
Bioinformatics 2003, 19:22462253. PubMed Abstract  Publisher Full Text

Tibshirani R: Regression shrinkage and selection via the lasso.

Fiedman J, Hastie T, Hofling H, Tibshirani R: Path wise coordinate optimization.
Ann. Appl. Statist. 2007, 1:302332. Publisher Full Text

Fiedman J, Hastie T, Hofling H, Tibshirani R: Regularization paths for generalized linear models via coordinate descent.

Gavin CC, Talbot LC: Gene selection in cancer classification using sparse logistic regression with Bayesian regularization.
Bioinformatics 2006, 22:23482355. PubMed Abstract  Publisher Full Text

Xu ZB, Zhang H, Wang Y, Chang XY, Liang Y: L_{1/2} regularization.

Fan J, Li R: Variable selection via nonconcave penalized likelihood and its oracle properties.
J. Amer. Statist. Assoc. 2001, 96:13481361. Publisher Full Text

Zou H, Hastie T: Regularization and variable selection via the elastic net.
J Royal Stat Soc Series B 2005, 67(2):301320. Publisher Full Text

Zhang CH: Nearly unbiased variable selection under minimax concave penalty.
Ann. Statist. 2010, 38:894942. Publisher Full Text

Xu ZB, Chang XY, Xu FM, Zhang H: L_{1/2} Regularization: a thresholding representation theory and a fast solver.
IEEE Transact Neural Networks Learn Syst 2012, 23(7):10131027.

Sohn I, Kim J, Jung SH, Park C: Gradient lasso for Cox proportional hazards model.
Bioinformatics 2009, 25(14):17751781. PubMed Abstract  Publisher Full Text

Yang K, Cai ZP, Li JZ, Lin GH: A stable gene selection in microarray data analysis.
BMC Bioinformatics 2006, 7:228. PubMed Abstract  BioMed Central Full Text  PubMed Central Full Text

Alon U, Barkai N, Notterman D, Gish K, Ybarra S, Mack D, Levine A: Broad patterns of gene expression revealed by clustering analysis of tumor and normal colon tissues probed by oligonucleotide arrays.
Proc Nat Acad Sci USA 1999, 96(12):67456750. PubMed Abstract  Publisher Full Text  PubMed Central Full Text

Shipp MA, Ross KN, Tamayo P, Weng AP, Kutok JL, Aguiar RC, Gaasenbeek M, Amgel M, Reich M, Pinkus GS, Ray TS, Kovall MA, Last KW, Norton A, Lister TA, Mesirov J, Neuberg DS, Lander ES, Aster JC, Golub TR: Diffuse large Bcell lymphoma outcome prediction by gene expression profiling and supervised machine learning.
Nat Med 2002, 8:6874. PubMed Abstract  Publisher Full Text

Nagai A, Terashima M, Harada T, Shimode K, Takeuchi H, Murakawa Y, et al.: Cathepsin B and H activities and cystatin C concentrations in cerebrospinal fluid from patients with leptomeningeal metastasis.
Clin Chim Acta 2003, 329:5360. PubMed Abstract  Publisher Full Text

Moroz C, Traub L, Maymon R, Zahalka MA: A novel human ferritin subunit from placenta with immunosuppressive activity.
J Biol Chem 2002, 277:1290112905. PubMed Abstract  Publisher Full Text

BenDor A, et al.: Tissue classification with gene expression profiles.
J Comput Biol 2000, 7:559583. PubMed Abstract  Publisher Full Text

Yang AJ, Song XY: Bayesian variable selection for disease classification using gene expression data.
Bioinformatics 2010, 26:215222. PubMed Abstract  Publisher Full Text

Li HD, Xu QS, Liang YZ: Random frog: an efficient reversible jump Markov chain Monte Carlolike approach for variable selection with applications to gene selection and disease classification.
Anal Chim Acta 2012, 740:2026. PubMed Abstract  Publisher Full Text

Notterman DA, Alon U, Sierk AJ, Levine AJ: Minimax probability machine. Advances in neural processing systems.
Cancer Res 2001, 61:31243130. PubMed Abstract  Publisher Full Text

Shailubhai K, Yu H, Karunanandaa K, Wang J, Eber S, Wang Y, Joo N, Kim H, Miedema B, Abbas S, Boddupalli S, Currie M, Forte L: Uroguanylin treatment suppeesses polyp formation in the Apc(Min/+) mouse and indices apoptosis in human colon adenocarcinoma cells via cyclic GMP.
Cancer Res 2000, 60:51515157. PubMed Abstract  Publisher Full Text

Maglietta R, Addabbo A, Piepoli A, Perri F, Liuni S, Pesole G, Ancona N: Selection of relevant genes in cancer diagnosis based on their prediction accuracy.
Art Intell Med 2007, 40:2944. Publisher Full Text

Wiese AH J, Lassmann S, Nahrig J, Rosenberg R, Hofler H, Ruger R, Werner M: Identification of gene signatures for invasive colorectal tumor cells.
Cancer Detect Prev 2007, 31:282295. PubMed Abstract  Publisher Full Text

Wang SL, Li XL, Zhang SW, Gui J, Huang DS: Tumor classification by combining PNN classifier ensemble with neighborhood rough set based gene reduction.
Comp Biol Med 2010, 40:179189. Publisher Full Text

Dai JH, Xu Q: Attribute selection based on information gain ratio in fuzzy rough set theory with application to tumor classification.
App Soft Comp 2013, 13:211221. Publisher Full Text