Variable Selection in Nonparametric Varying-Coefficient Models for Analysis of Repeated Measurements
重复测量分析中非参数变系数模型的变量选择AI 解读 ↓
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重复测量分析中非参数变系数模型的变量选择AI 解读 ↓
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Nonparametric varying-coefficient models are commonly used for analysis of data measured repeatedly over time, including longitudinal and functional responses data. While many procedures have been developed for estimating the varying-coefficients, the problem of variable selection for such models has not been addressed. In this article, we present a regularized estimation procedure for variable selection that combines basis function approximations and the smoothly clipped absolute deviation (SCAD) penalty. The proposed procedure simultaneously selects significant variables with time-varying effects and estimates the nonzero smooth coefficient functions. Under suitable conditions, we have established the theoretical properties of our procedure, including consistency in variable selection and the oracle property in estimation. Here the oracle property means that the asymptotic distribution of an estimated coefficient function is the same as that when it is known a priori which variables are in the model. The method is illustrated with simulations and two real data examples, one for identifying risk factors in the study of AIDS and one using microarray time-course gene expression data to identify the transcription factors related to the yeast cell cycle process.
具有异质性的非参数时变面板模型
Since Bai (2009, Econometrica 77, 1229–1279), considerable extensions have been made to panel data models with interactive fixed effects (IFEs). However, little work has been conducted to understand the associated iterative algorithm, which, to the best of our knowledge, is the most commonly adopted approach in this line of research. In this paper, we refine the algorithm of panel data models with IFEs using the nuclear-norm penalization method and duple least-squares (DLS)…
不可观测异质性的去偏机器学习:高维面板与测量误差模型
Developing robust inference for models with nonparametric Unobserved Heterogeneity (UH) is both important and challenging. We propose novel Debiased Machine Learning (DML) procedures for valid inference on functionals of UH, allowing for partial identification of multivariate target and high-dimensional nuisance parameters. Our main contribution is a full characterization of all relevant Neyman-orthogonal moments in models with nonparametric UH, where relevance means…
时变面板数据模型中潜在分组结构的估计
We consider panel data models where coefficients change smoothly over time and follow a latent group structure, being homogeneous within but heterogeneous across groups. To jointly estimate the group membership and group-specific coefficient trajectories, we propose FUSE-TIME, a pairwise adaptive group fused-Lasso estimator combined with polynomial spline sieves. We establish consistency, derive the asymptotic distributions of the penalized sieve estimator and its…
具有时变潜在分组结构的面板数据模型
This paper considers a linear panel model with interactive fixed effects and unobserved individual and time heterogeneities that are captured by some latent group structures and an unknown structural break, respectively. To enhance realism, the model may have different numbers of groups and/or different group memberships before and after the break. With preliminary nuclear norm regularized estimation followed by row- and column-wise linear regressions, we estimate the break…
具有时变潜在分组结构的面板数据模型
This paper considers a linear panel model with interactive fixed effects and unobserved individual and time heterogeneities that are captured by some latent group structures and an unknown structural break, respectively. To enhance realism the model may have different numbers of groups and/or different group memberships before and after the break. With the preliminary nuclear-norm-regularized estimation followed by row- and column-wise linear regressions, we estimate the…
纵向数据的超高维分位数回归:血压分析应用
Despite major advances in research and treatment, identifying important genotype risk factors for high blood pressure remains challenging. Traditional genome-wide association studies (GWAS) focus on one single nucleotide polymorphism (SNP) at a time. We aim to select among over half a million SNPs along with time-varying phenotype variables via simultaneous modeling and variable selection, focusing on the most dangerous blood pressure levels at high quantiles. Taking…