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DoHwan Park

Publications and source records attributed to DoHwan Park.

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Two-Stage Multiple Test Procedures Controlling False Discovery Rate with auxiliary variable and their Application to Set4Delta Mutant Data

In this paper, we present novel methodologies that incorporate auxiliary variables for multiple hypotheses testing related to the main point of interest while effectively controlling the false discovery rate. When dealing with multiple tests concerning the primary variable of interest, researchers can use auxiliary variables to set preconditions for the significance of primary variables, thereby enhancing test efficacy. Depending on the auxiliary variable's role, we propose two approaches: one terminates testing of the primary variable if it does not meet predefined conditions, and the other adjusts the evaluation criteria based on the auxiliary variable. Employing the copula method, we elucidate the dependence between the auxiliary and primary variables by deriving their joint distribution from individual marginal distributions.Our numerical studies, compared with existing methods, demonstrate that the proposed methodologies effectively control the FDR and yield greater statistical power than previous approaches solely based on the primary variable. As an illustrative example, we apply our methods to the Set4$\Delta$ mutant dataset. Our findings highlight the distinctions between our methodologies and traditional approaches, emphasising the potential advantages of our methods in introducing the auxiliary variable for selecting more genes.

stat.ME

Empirical Null Estimation using Discrete Mixture Distributions and its Application to Protein Domain Data

In recent mutation studies, analyses based on protein domain positions are gaining popularity over gene-centric approaches since the latter have limitations in considering the functional context that the position of the mutation provides. This presents a large-scale simultaneous inference problem, with hundreds of hypothesis tests to consider at the same time. This paper aims to select significant mutation counts while controlling a given level of Type I error via False Discovery Rate (FDR) procedures. One main assumption is that there exists a cut-off value such that smaller counts than this value are generated from the null distribution. We present several data-dependent methods to determine the cut-off value. We also consider a two-stage procedure based on screening process so that the number of mutations exceeding a certain value should be considered as significant mutations. Simulated and protein domain data sets are used to illustrate this procedure in estimation of the empirical null using a mixture of discrete distributions.

stat.ME