The spike‐and‐slab quantile LASSO for robust variable selection in cancer genomics studies

Author:

Liu Yuwen1,Ren Jie2,Ma Shuangge3ORCID,Wu Cen1ORCID

Affiliation:

1. Department of Statistics Kansas State University Manhattan Kansas USA

2. Department of Biostatistics and Health Data Sciences Indiana University School of Medicine Indianapolis Indiana USA

3. Department of Biostatistics Yale University New Haven Connecticut USA

Abstract

Data irregularity in cancer genomics studies has been widely observed in the form of outliers and heavy‐tailed distributions in the complex traits. In the past decade, robust variable selection methods have emerged as powerful alternatives to the nonrobust ones to identify important genes associated with heterogeneous disease traits and build superior predictive models. In this study, to keep the remarkable features of the quantile LASSO and fully Bayesian regularized quantile regression while overcoming their disadvantage in the analysis of high‐dimensional genomics data, we propose the spike‐and‐slab quantile LASSO through a fully Bayesian spike‐and‐slab formulation under the robust likelihood by adopting the asymmetric Laplace distribution (ALD). The proposed robust method has inherited the prominent properties of selective shrinkage and self‐adaptivity to the sparsity pattern from the spike‐and‐slab LASSO (Roc̆ková and George, J Am Stat Associat, 2018, 113(521): 431–444). Furthermore, the spike‐and‐slab quantile LASSO has a computational advantage to locate the posterior modes via soft‐thresholding rule guided Expectation‐Maximization (EM) steps in the coordinate descent framework, a phenomenon rarely observed for robust regularization with nondifferentiable loss functions. We have conducted comprehensive simulation studies with a variety of heavy‐tailed errors in both homogeneous and heterogeneous model settings to demonstrate the superiority of the spike‐and‐slab quantile LASSO over its competing methods. The advantage of the proposed method has been further demonstrated in case studies of the lung adenocarcinomas (LUAD) and skin cutaneous melanoma (SKCM) data from The Cancer Genome Atlas (TCGA).

Funder

National Institutes of Health

Publisher

Wiley

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