Shrinkage-to-Tapering Estimation of Large Covariance Matrices

被引:35
作者
Chen, Xiaohui [1 ]
Wang, Z. Jane [1 ]
McKeown, Martin J. [2 ]
机构
[1] Univ British Columbia, Dept Elect & Comp Engn, Vancouver, BC V6T 1Z4, Canada
[2] Univ British Columbia, Dept Med Neurol, Vancouver, BC V6T 2B5, Canada
关键词
Large covariance estimation; minimax risk; minimum mean-squared errors; shrinkage estimator; tapering operator;
D O I
10.1109/TSP.2012.2210546
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
In this paper, we introduce a shrinkage-to-tapering approach for estimating large covariance matrices when the number of samples is substantially fewer than the number of variables (i.e., n, p -> infinity and p/n -> infinity). The proposed estimator improves upon both shrinkage and tapering estimators by shrinking the sample covariance matrix to its tapered version. We first show that, under both normalized Frobenius and spectral risks, the minimum mean-squared error (MMSE) shrinkage-to-identity estimator is inconsistent and outperformed by a minimax tapering estimator for a class of high-dimensional and diagonally dominant covariance matrices. Motivated by this observation, we propose a shrinkage-to-tapering oracle (STO) estimator for efficient estimation of general, large covariance matrices. A closed-form formula of the optimal coefficient rho of the proposed STO estimator is derived under the minimum Frobenius risk. Since the true covariance matrix is to be estimated, we further propose a STO approximating (STOA) algorithm with a data-driven bandwidth selection procedure to iteratively estimate the coefficient rho and the covariance matrix. We study the finite sample performances of different estimators and our simulation results clearly show the improved performances of the proposed STO estimators. Finally, the proposed STOA method is applied to a real breast cancer gene expression data set.
引用
收藏
页码:5640 / 5656
页数:17
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