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An extended sequential goodness-of-fit multiple testing method for discrete data
Irene Castro-Conde1, Sebastian Döhler2, Jacobo de Uña-Álvarez3
11 Faculty of Economics, SiDOR Research Group & Centro de Investigaciones Biomédicas (CINBIO), University of Vigo, Spain.
A new sequential goodness-of-fit (SGoF) method improves multiple testing for discrete data. This enhanced procedure is more powerful and achieves better false discovery rate control than the original SGoF method.
Area of Science:
- Biostatistics
- Statistical methodology
- High-dimensional data analysis
Background:
- The sequential goodness-of-fit (SGoF) method is a recent approach for multiple testing, particularly in high-dimensional settings.
- Traditional SGoF can be overly conservative when dealing with discrete test statistics.
- Existing methods for controlling familywise error rate (FWER) and false discovery rate (FDR) may lack power in high-dimensional scenarios.
Purpose of the Study:
- To introduce a modified SGoF procedure that accounts for the discreteness of test statistics.
- To develop a more powerful multiple testing method for discrete data compared to the original SGoF.
- To achieve false discovery rate (FDR) levels closer to the nominal level while maintaining weak control.
Main Methods:
- Development of an alternative SGoF-type procedure incorporating discrete test statistic adjustments.
- Simulation studies to evaluate the performance and power of the new method.
- Application of the proposed method to a real-world pharmacovigilance dataset.
Main Results:
- The proposed SGoF-type method demonstrates improved power compared to the original SGoF.
- The new procedure achieves false discovery rate (FDR) levels closer to the desired nominal level.
- The method shows effective control of the familywise error rate (FWER) and false discovery rate (FDR) in simulations.
Conclusions:
- The modified SGoF procedure offers a more powerful and accurate alternative for multiple testing with discrete data.
- This method provides a valuable tool for analyzing high-dimensional data where test statistics are discrete.
- The approach is applicable to real-world problems, such as in pharmacovigilance studies.
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