Christian Chan , Xiaotian Dai , Thierry Chekouo , Quan Long , Xuewen Lu
{"title":"广义部分线性模型变量选择的破碎自适应脊法及其在冠心病数据中的应用","authors":"Christian Chan , Xiaotian Dai , Thierry Chekouo , Quan Long , Xuewen Lu","doi":"10.1016/j.jcmds.2025.100127","DOIUrl":null,"url":null,"abstract":"<div><div>Motivated by the CATHGEN data, we develop a new statistical method for simultaneous variable selection and parameter estimation in the context of generalized partly linear models for data with high-dimensional covariates. The method is referred to as the broken adaptive ridge (BAR) estimator, which is an approximation of the <span><math><msub><mrow><mi>L</mi></mrow><mrow><mn>0</mn></mrow></msub></math></span>-penalized regression by iteratively performing reweighted squared <span><math><msub><mrow><mi>L</mi></mrow><mrow><mn>2</mn></mrow></msub></math></span>-penalized regression. The generalized partly linear model extends the generalized linear model by incorporating a non-parametric component, allowing for the construction of a flexible model to capture various types of covariate effects. We employ the Bernstein polynomials as the sieve space to approximate the non-parametric functions so that our method can be implemented easily using the existing R packages. Extensive simulation studies suggest that the proposed method performs better than other commonly used penalty-based variable selection methods. We apply the method to the CATHGEN data with a binary response from a coronary artery disease study, which motivated our research, and obtained new findings in both high-dimensional genetic and low-dimensional non-genetic covariates.</div></div>","PeriodicalId":100768,"journal":{"name":"Journal of Computational Mathematics and Data Science","volume":"17 ","pages":"Article 100127"},"PeriodicalIF":0.0000,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Broken adaptive ridge method for variable selection in generalized partly linear models with application to the coronary artery disease data\",\"authors\":\"Christian Chan , Xiaotian Dai , Thierry Chekouo , Quan Long , Xuewen Lu\",\"doi\":\"10.1016/j.jcmds.2025.100127\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Motivated by the CATHGEN data, we develop a new statistical method for simultaneous variable selection and parameter estimation in the context of generalized partly linear models for data with high-dimensional covariates. The method is referred to as the broken adaptive ridge (BAR) estimator, which is an approximation of the <span><math><msub><mrow><mi>L</mi></mrow><mrow><mn>0</mn></mrow></msub></math></span>-penalized regression by iteratively performing reweighted squared <span><math><msub><mrow><mi>L</mi></mrow><mrow><mn>2</mn></mrow></msub></math></span>-penalized regression. The generalized partly linear model extends the generalized linear model by incorporating a non-parametric component, allowing for the construction of a flexible model to capture various types of covariate effects. We employ the Bernstein polynomials as the sieve space to approximate the non-parametric functions so that our method can be implemented easily using the existing R packages. Extensive simulation studies suggest that the proposed method performs better than other commonly used penalty-based variable selection methods. We apply the method to the CATHGEN data with a binary response from a coronary artery disease study, which motivated our research, and obtained new findings in both high-dimensional genetic and low-dimensional non-genetic covariates.</div></div>\",\"PeriodicalId\":100768,\"journal\":{\"name\":\"Journal of Computational Mathematics and Data Science\",\"volume\":\"17 \",\"pages\":\"Article 100127\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Computational Mathematics and Data Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772415825000197\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Computational Mathematics and Data Science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772415825000197","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Broken adaptive ridge method for variable selection in generalized partly linear models with application to the coronary artery disease data
Motivated by the CATHGEN data, we develop a new statistical method for simultaneous variable selection and parameter estimation in the context of generalized partly linear models for data with high-dimensional covariates. The method is referred to as the broken adaptive ridge (BAR) estimator, which is an approximation of the -penalized regression by iteratively performing reweighted squared -penalized regression. The generalized partly linear model extends the generalized linear model by incorporating a non-parametric component, allowing for the construction of a flexible model to capture various types of covariate effects. We employ the Bernstein polynomials as the sieve space to approximate the non-parametric functions so that our method can be implemented easily using the existing R packages. Extensive simulation studies suggest that the proposed method performs better than other commonly used penalty-based variable selection methods. We apply the method to the CATHGEN data with a binary response from a coronary artery disease study, which motivated our research, and obtained new findings in both high-dimensional genetic and low-dimensional non-genetic covariates.