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Fangyong Zheng

Publications and source records attributed to Fangyong Zheng.

2 recordsLinked to original sources

Revisiting dependence in multiple testing: empirical distribution approaches for FDP control

Large-scale multiple hypothesis testing is central to the analysis of high-throughput data, where controlling false discoveries is critical. Classical procedures typically rely on theoretical null distributions and often adjust for dependence among test statistics, but these approaches may be misleading when the empirical distribution of null statistics deviates from theoretical assumptions. Motivated by this observation, we investigate the role of the empirical cumulative distribution function (c.d.f.) of null test statistics in controlling the false discovery proportion (FDP). We first show that, under an oracle scenario where the empirical c.d.f. of the test statistics for all null hypotheses is known, FDP control can be achieved optimally regardless of the dependence structure, highlighting that explicit modeling of dependence may be unnecessary. Building on this insight, we propose an empirical c.d.f.-based FDP control (eFDP) method, implemented via a multivariate mixture model framework and a nonparametric estimation procedure for the empirical c.d.f.s, establish its asymptotic convergence, and construct an FDP control procedure that achieves asymptotic FDP control. Extensive simulations demonstrate that eFDP attains more accurate FDP control and higher power than existing approaches, particularly under strong dependence, and analysis of a high-dimensional breast cancer gene expression dataset confirms its practical utility.

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Maximum smoothed likelihood method for the combination of multiple diagnostic tests, with application to the ROC estimation

In medical diagnostics, leveraging multiple biomarkers can significantly improve classification accuracy compared to using a single biomarker. While existing methods based on exponential tilting or density ratio models have shown promise, their assumptions may be overly restrictive in practice. In this paper, we adopt a flexible semiparametric model that relates the density ratio of diseased to healthy subjects through an unknown monotone transformation of a linear combination of biomarkers. To enhance estimation efficiency, we propose a smoothed likelihood framework that exploits the smoothness in the underlying densities and transformation function. Building on the maximum smoothed likelihood methodology, we construct estimators for the model parameters and the associated probability density functions. We develop an effective computational algorithm for implementation, derive asymptotic properties of the proposed estimators, and establish procedures for estimating the receiver operating characteristic (ROC) curve and the area under the curve (AUC). Through simulation studies and a real-data application, we demonstrate that the proposed method yields more accurate and efficient estimates than existing approaches.

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