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AI 根据所提供的论文材料归类:摘要研究一般半监督回归及医疗数据应用,未明确对应所列经济金融细分领域。

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关注这篇论文的作者
Tianxi Cai

半监督环境下高效且自适应的线性回归

研究问题
当有标签数据较少、无标签协变量数据较多时,何时能够利用后者提高线性回归参数估计效率,并适应模型误设?
方法与思路
作者提出两步 EASE 估计,结合灵活的半非参数插补、平滑、再拟合和交叉验证,并以双重交叉验证进行推断。
材料陈述的贡献
摘要称方法在误设下提高效率、在线性模型成立时保持最优效率,并建立一致性、渐近正态性及影响函数展开。
阅读关注点
应核对误设下回归参数的目标定义、两类样本的关系、效率最优的适用情形,以及平滑和交叉验证所需条件。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明;具体效率界、样本条件和改进幅度未说明,“安全”使用的边界需全文核对。

原文摘要

We consider the linear regression problem under semi-supervised settings wherein the available data typically consists of: (i) a small or moderate sized “labeled” data, and (ii) a much larger sized “unlabeled” data. Such data arises naturally from settings where the outcome, unlike the covariates, is expensive to obtain, a frequent scenario in modern studies involving large databases like electronic medical records (EMR). Supervised estimators like the ordinary least squares (OLS) estimator utilize only the labeled data. It is often of interest to investigate if and when the unlabeled data can be exploited to improve estimation of the regression parameter in the adopted linear model. In this paper, we propose a class of “Efficient and Adaptive Semi-Supervised Estimators” (EASE) to improve estimation efficiency. The EASE are two-step estimators adaptive to model mis-specification, leading to improved (optimal in some cases) efficiency under model mis-specification, and equal (optimal) efficiency under a linear model. This adaptive property, often unaddressed in the existing literature, is crucial for advocating “safe” use of the unlabeled data. The construction of EASE primarily involves a flexible “semi-nonparametric” imputation, including a smoothing step that works well even when the number of covariates is not small; and a follow up “refitting” step along with a cross-validation (CV) strategy both of which have useful practical as well as theoretical implications towards addressing two important issues: under-smoothing and over-fitting. We establish asymptotic results including consistency, asymptotic normality and the adaptive properties of EASE. We also provide influence function expansions and a “double” CV strategy for inference. The results are further validated through extensive simulations, followed by application to an EMR study on auto-immunity.

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