arXiv subjects

Tiejun Tong

Publications and source records attributed to Tiejun Tong.

29 records · Page 2Linked to original sources

arXiv2018

Diagonal Likelihood Ratio Test for Equality of Mean Vectors in High-Dimensional Data

We propose a likelihood ratio test framework for testing normal mean vectors in high-dimensional data under two common scenarios: the one-sample test and the two-sample test with equal covariance matrices. We derive the test statistics under the assumption that the covariance matrices follow a diagonal matrix structure. In comparison with the diagonal Hotelling's tests, our proposed test statistics display some interesting characteristics. In particular, they are a summation of the log-transformed squared $t$-statistics rather than a direct summation of those components. More importantly, to derive the asymptotic normality of our test statistics under the null and local alternative hypotheses, we do not need the requirement that the covariance matrices follow a diagonal matrix structure. As a consequence, our proposed test methods are very flexible and readily applicable in practice. Simulation studies and a real data analysis are also carried out to demonstrate the advantages of our likelihood ratio test methods.

stat.ME↗

arXiv2018

Varying Coefficient Panel Data Model with Interactive Fixed Effects

In this paper, we propose a varying coefficient panel data model with unobservable multiple interactive fixed effects that are correlated with the regressors. We approximate each coefficient function by B-spline, and propose a robust nonlinear iteration scheme based on the least squares method to estimate the coefficient functions of interest. We also establish the asymptotic theory of the resulting estimators under certain regularity assumptions, including the consistency, the convergence rate and the asymptotic distribution. Furthermore, we develop a least squares dummy variable method to study an important special case of the proposed model: the varying coefficient panel data model with additive fixed effects. To construct the pointwise confidence intervals for the coefficient functions, a residual-based block bootstrap method is proposed to reduce the computational burden as well as to avoid the accumulative errors. Simulation studies and a real data analysis are also carried out to assess the performance of our proposed methods.

stat.ME↗

arXiv2018

Testing normality using the summary statistics with application to meta-analysis

As the most important tool to provide high-level evidence-based medicine, researchers can statistically summarize and combine data from multiple studies by conducting meta-analysis. In meta-analysis, mean differences are frequently used effect size measurements to deal with continuous data, such as the Cohen's d statistic and Hedges' g statistic values. To calculate the mean difference based effect sizes, the sample mean and standard deviation are two essential summary measures. However, many of the clinical reports tend not to directly record the sample mean and standard deviation. Instead, the sample size, median, minimum and maximum values and/or the first and third quartiles are reported. As a result, researchers have to transform the reported information to the sample mean and standard deviation for further compute the effect size. Since most of the popular transformation methods were developed upon the normality assumption of the underlying data, it is necessary to perform a pre-test before transforming the summary statistics. In this article, we had introduced test statistics for three popular scenarios in meta-analysis. We suggests medical researchers to perform a normality test of the selected studies before using them to conduct further analysis. Moreover, we applied three different case studies to demonstrate the usage of the newly proposed test statistics. The real data case studies indicate that the new test statistics are easy to apply in practice and by following the recommended path to conduct the meta-analysis, researchers can obtain more reliable conclusions.

stat.ME↗

arXiv2018

TFisher Tests: Optimal and Adaptive Thresholding for Combining $p$-Values

For testing a group of hypotheses, tremendous $p$-value combination methods have been developed and widely applied since 1930's. Some methods (e.g., the minimal $p$-value) are optimal for sparse signals, and some others (e.g., Fisher's combination) are optimal for dense signals. To address a wide spectrum of signal patterns, this paper proposes a unifying family of statistics, called TFisher, with general $p$-value truncation and weighting schemes. Analytical calculations for the $p$-value and the statistical power of TFisher under general hypotheses are given. Optimal truncation and weighting parameters are studied based on Bahadur Efficiency (BE) and the proposed Asymptotic Power Efficiency (APE), which is superior to BE for studying the signal detection problem. A soft-thresholding scheme is shown to be optimal for signal detection in a large space of signal patterns. When prior information of signal pattern is unavailable, an omnibus test, oTFisher, can adapt to the given data. Simulations evidenced the accuracy of calculations and validated the theoretical properties. The TFisher tests were applied to analyzing a whole exome sequencing data of amyotrophic lateral sclerosis. Relevant tests and calculations have been implemented into an R package $TFisher$ and published on the CRAN.

stat.ME↗

arXiv2018

How to estimate the sample mean and standard deviation from the five number summary?

In some clinical studies, researchers may report the five number summary (including the sample median, the first and third quartiles, and the minimum and maximum values) rather than the sample mean and standard deviation. To conduct meta-analysis for pooling studies, one needs to first estimate the sample mean and standard deviation from the five number summary. A number of studies have been proposed in the recent literature to solve this problem. However, none of the existing estimators for the standard deviation is satisfactory for practical use. After a brief review of the existing literature, we point out that Wan et al.'s method (BMC Med Res Methodol 14:135, 2014) has a serious limitation in estimating the standard deviation from the five number summary. To improve it, we propose a smoothly weighted estimator by incorporating the sample size information and derive the optimal weight for the new estimator. For ease of implementation, we also provide an approximation formula of the optimal weight and a shortcut formula for estimating the standard deviation from the five number summary. The performance of the proposed estimator is evaluated through two simulation studies. In comparison with Wan et al.'s estimator, our new estimator provides a more accurate estimate for normal data and performs favorably for non-normal data. In real data analysis, our new method is also able to provide a more accurate estimate of the true sample standard deviation than the existing method. In this paper, we propose an optimal estimator of the standard deviation from the five number summary. Together with the optimal mean estimator in Luo et al. (Stat Methods Med Res, in press, 2017), our new methods have improved the existing literature and will make a solid contribution to meta-analysis and evidence-based medicine.

stat.ME↗

arXiv2016

SIMEX estimation for single-index model with covariate measurement error

In this paper, we consider the single-index measurement error model with mismeasured covariates in the nonparametric part. To solve the problem, we develop a simulation-extrapolation (SIMEX) algorithm based on the local linear smoother and the estimating equation. For the proposed SIMEX estimation, it is not needed to assume the distribution of the unobserved covariate. We transform the boundary of a unit ball in $\mathbb{R}^p$ to the interior of a unit ball in $\mathbb{R}^{p-1}$ by using the constraint $\|β\|=1$. The proposed SIMEX estimator of the index parameter is shown to be asymptotically normal under some regularity conditions. We also derive the asymptotic bias and variance of the estimator of the unknown link function. Finally, the performance of the proposed method is examined by simulation studies and is illustrated by a real data example.

stat.ME↗

arXiv2016

Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range

In systematic reviews and meta-analysis, researchers often pool the results of the sample mean and standard deviation from a set of similar clinical trials. A number of the trials, however, reported the study using the median, the minimum and maximum values, and/or the first and third quartiles. Hence, in order to combine results, one may have to estimate the sample mean and standard deviation for such trials. In this paper, we propose to improve the existing literature in several directions. First, we show that the sample standard deviation estimation in Hozo et al. (2005) has some serious limitations and is always less satisfactory in practice. Inspired by this, we propose a new estimation method by incorporating the sample size. Second, we systematically study the sample mean and standard deviation estimation problem under more general settings where the first and third quartiles are also available for the trials. Through simulation studies, we demonstrate that the proposed methods greatly improve the existing methods and enrich the literature. We conclude our work with a summary table that serves as a comprehensive guidance for performing meta-analysis in different situations.

stat.ME↗

arXiv2016

Optimally estimating the sample mean from the sample size, median, mid-range and/or mid-quartile range

The era of big data is coming, and evidence-based medicine is attracting increasing attention to improve decision making in medical practice via integrating evidence from well designed and conducted clinical research. Meta-analysis is a statistical technique widely used in evidence-based medicine for analytically combining the findings from independent clinical trials to provide an overall estimation of a treatment effectiveness. The sample mean and standard deviation are two commonly used statistics in meta-analysis but some trials use the median, the minimum and maximum values, or sometimes the first and third quartiles to report the results. Thus, to pool results in a consistent format, researchers need to transform those information back to the sample mean and standard deviation. In this paper, we investigate the optimal estimation of the sample mean for meta-analysis from both theoretical and empirical perspectives. A major drawback in the literature is that the sample size, needless to say its importance, is either ignored or used in a stepwise but somewhat arbitrary manner, e.g., the famous method proposed by Hozo et al. We solve this issue by incorporating the sample size in a smoothly changing weight in the estimators to reach the optimal estimation. Our proposed estimators not only improve the existing ones significantly but also share the same virtue of the simplicity. The real data application indicates that our proposed estimators are capable to serve as "rules of thumb" and will be widely applied in evidence-based medicine.

stat.ME↗

arXiv2015

NBLDA: Negative Binomial Linear Discriminant Analysis for RNA-Seq Data

RNA-sequencing (RNA-Seq) has become a powerful technology to characterize gene expression profiles because it is more accurate and comprehensive than microarrays. Although statistical methods that have been developed for microarray data can be applied to RNA-Seq data, they are not ideal due to the discrete nature of RNA-Seq data. The Poisson distribution and negative binomial distribution are commonly used to model count data. Recently, Witten (2011) proposed a Poisson linear discriminant analysis for RNA-Seq data. The Poisson assumption may not be as appropriate as negative binomial distribution when biological replicates are available and in the presence of overdispersion (i.e., when the variance is larger than the mean). However, it is more complicated to model negative binomial variables because they involve a dispersion parameter that needs to be estimated. In this paper, we propose a negative binomial linear discriminant analysis for RNA-Seq data. By Bayes' rule, we construct the classifier by fitting a negative binomial model, and propose some plug-in rules to estimate the unknown parameters in the classifier. The relationship between the negative binomial classifier and the Poisson classifier is explored, with a numerical investigation of the impact of dispersion on the discriminant score. Simulation results show the superiority of our proposed method. We also analyze four real RNA-Seq data sets to demonstrate the advantage of our method in real-world applications.

stat.AP↗

arXiv2014

Non-parametric shrinkage mean estimation for quadratic loss functions with unknown covariance matrices

In this paper, a shrinkage estimator for the population mean is proposed under known quadratic loss functions with unknown covariance matrices. The new estimator is non-parametric in the sense that it does not assume a specific parametric distribution for the data and it does not require the prior information on the population covariance matrix. Analytical results on the improvement of the proposed shrinkage estimator are provided and some corresponding asymptotic properties are also derived. Finally, we demonstrate the practical improvement of the proposed method over existing methods through extensive simulation studies and real data analysis. Keywords: High-dimensional data; Shrinkage estimator; Large $p$ small $n$; $U$-statistic.

stat.ME↗

arXiv2013

Optimal variance estimation without estimating the mean function

We study the least squares estimator in the residual variance estimation context. We show that the mean squared differences of paired observations are asymptotically normally distributed. We further establish that, by regressing the mean squared differences of these paired observations on the squared distances between paired covariates via a simple least squares procedure, the resulting variance estimator is not only asymptotically normal and root-$n$ consistent, but also reaches the optimal bound in terms of estimation variance. We also demonstrate the advantage of the least squares estimator in comparison with existing methods in terms of the second order asymptotic properties.

math.ST↗