No Arabic abstract
This paper proposes an innovative method for constructing confidence intervals and assessing p-values in statistical inference for high-dimensional linear models. The proposed method has successfully broken the high-dimensional inference problem into a series of low-dimensional inference problems: For each regression coefficient $beta_i$, the confidence interval and $p$-value are computed by regressing on a subset of variables selected according to the conditional independence relations between the corresponding variable $X_i$ and other variables. Since the subset of variables forms a Markov neighborhood of $X_i$ in the Markov network formed by all the variables $X_1,X_2,ldots,X_p$, the proposed method is coined as Markov neighborhood regression. The proposed method is tested on high-dimensional linear, logistic and Cox regression. The numerical results indicate that the proposed method significantly outperforms the existing ones. Based on the Markov neighborhood regression, a method of learning causal structures for high-dimensional linear models is proposed and applied to identification of drug sensitive genes and cancer driver genes. The idea of using conditional independence relations for dimension reduction is general and potentially can be extended to other high-dimensional or big data problems as well.
Among the most popular variable selection procedures in high-dimensional regression, Lasso provides a solution path to rank the variables and determines a cut-off position on the path to select variables and estimate coefficients. In this paper, we consider variable selection from a new perspective motivated by the frequently occurred phenomenon that relevant variables are not completely distinguishable from noise variables on the solution path. We propose to characterize the positions of the first noise variable and the last relevant variable on the path. We then develop a new variable selection procedure to control over-selection of the noise variables ranking after the last relevant variable, and, at the same time, retain a high proportion of relevant variables ranking before the first noise variable. Our procedure utilizes the recently developed covariance test statistic and Q statistic in post-selection inference. In numerical examples, our method compares favorably with other existing methods in selection accuracy and the ability to interpret its results.
With the availability of high dimensional genetic biomarkers, it is of interest to identify heterogeneous effects of these predictors on patients survival, along with proper statistical inference. Censored quantile regression has emerged as a powerful tool for detecting heterogeneous effects of covariates on survival outcomes. To our knowledge, there is little work available to draw inference on the effects of high dimensional predictors for censored quantile regression. This paper proposes a novel procedure to draw inference on all predictors within the framework of global censored quantile regression, which investigates covariate-response associations over an interval of quantile levels, instead of a few discrete values. The proposed estimator combines a sequence of low dimensional model estimates that are based on multi-sample splittings and variable selection. We show that, under some regularity conditions, the estimator is consistent and asymptotically follows a Gaussian process indexed by the quantile level. Simulation studies indicate that our procedure can properly quantify the uncertainty of the estimates in high dimensional settings. We apply our method to analyze the heterogeneous effects of SNPs residing in lung cancer pathways on patients survival, using the Boston Lung Cancer Survival Cohort, a cancer epidemiology study on the molecular mechanism of lung cancer.
Labeling patients in electronic health records with respect to their statuses of having a disease or condition, i.e. case or control statuses, has increasingly relied on prediction models using high-dimensional variables derived from structured and unstructured electronic health record data. A major hurdle currently is a lack of valid statistical inference methods for the case probability. In this paper, considering high-dimensional sparse logistic regression models for prediction, we propose a novel bias-corrected estimator for the case probability through the development of linearization and variance enhancement techniques. We establish asymptotic normality of the proposed estimator for any loading vector in high dimensions. We construct a confidence interval for the case probability and propose a hypothesis testing procedure for patient case-control labelling. We demonstrate the proposed method via extensive simulation studies and application to real-world electronic health record data.
There are many scenarios such as the electronic health records where the outcome is much more difficult to collect than the covariates. In this paper, we consider the linear regression problem with such a data structure under the high dimensionality. Our goal is to investigate when and how the unlabeled data can be exploited to improve the estimation and inference of the regression parameters in linear models, especially in light of the fact that such linear models may be misspecified in data analysis. In particular, we address the following two important questions. (1) Can we use the labeled data as well as the unlabeled data to construct a semi-supervised estimator such that its convergence rate is faster than the supervised estimators? (2) Can we construct confidence intervals or hypothesis tests that are guaranteed to be more efficient or powerful than the supervised estimators? To address the first question, we establish the minimax lower bound for parameter estimation in the semi-supervised setting. We show that the upper bound from the supervised estimators that only use the labeled data cannot attain this lower bound. We close this gap by proposing a new semi-supervised estimator which attains the lower bound. To address the second question, based on our proposed semi-supervised estimator, we propose two additional estimators for semi-supervised inference, the efficient estimator and the safe estimator. The former is fully efficient if the unknown conditional mean function is estimated consistently, but may not be more efficient than the supervised approach otherwise. The latter usually does not aim to provide fully efficient inference, but is guaranteed to be no worse than the supervised approach, no matter whether the linear model is correctly specified or the conditional mean function is consistently estimated.
Heterogeneity is an important feature of modern data sets and a central task is to extract information from large-scale and heterogeneous data. In this paper, we consider multiple high-dimensional linear models and adopt the definition of maximin effect (Meinshausen, B{u}hlmann, AoS, 43(4), 1801--1830) to summarize the information contained in this heterogeneous model. We define the maximin effect for a targeted population whose covariate distribution is possibly different from that of the observed data. We further introduce a ridge-type maximin effect to simultaneously account for reward optimality and statistical stability. To identify the high-dimensional maximin effect, we estimate the regression covariance matrix by a debiased estimator and use it to construct the aggregation weights for the maximin effect. A main challenge for statistical inference is that the estimated weights might have a mixture distribution and the resulted maximin effect estimator is not necessarily asymptotic normal. To address this, we devise a novel sampling approach to construct the confidence interval for any linear contrast of high-dimensional maximin effects. The coverage and precision properties of the proposed confidence interval are studied. The proposed method is demonstrated over simulations and a genetic data set on yeast colony growth under different environments.