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Signal identification for rare and weak features: higher criticism or false discovery rates?
Bernd Klaus1, Korbinian Strimmer
1Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Härtelstr. 16-18, D-04107 Leipzig, Germany.
Biostatistics (Oxford, England)
|September 11, 2012
Summary
The higher criticism (HC) threshold approximates the class boundary (CB) threshold for signal identification. In rare-weak settings, HC thresholding is equivalent to using a local false discovery rate (FDR) cutoff.
Area of Science:
- Biostatistics
- Statistical inference
- High-dimensional data analysis
Background:
- Signal identification in large-dimensional datasets presents significant challenges.
- The method of higher criticism (HC) has emerged as a valuable tool for setting decision thresholds.
- Understanding HC's performance within a false discovery rate (FDR) framework is crucial.
Purpose of the Study:
- To investigate the higher criticism (HC) method from a false discovery rate (FDR) perspective.
- To establish the relationship between HC thresholds and class boundary (CB) thresholds in discriminant analysis.
- To evaluate the practical equivalence of HC and FDR-based thresholds in specific data regimes.
Main Methods:
- Theoretical analysis of the higher criticism (HC) threshold in relation to class boundary (CB) thresholds.
- Investigation of the equivalence between HC thresholding and local FDR cutoffs.
- Empirical validation through simulations and application to real-world cancer gene expression data.
Main Results:
- The HC threshold serves as an approximation to the natural class boundary (CB) threshold.
- In rare-weak signal settings, HC thresholding is practically indistinguishable from using a local FDR cutoff.
- Analytical and simulation studies confirm the relationship and properties of HC and CB thresholds.
Conclusions:
- The higher criticism (HC) method provides an effective and interpretable approach to signal identification in high-dimensional data.
- HC thresholding aligns with FDR-based methods, offering a robust statistical framework.
- The findings are validated across diverse datasets, including cancer gene expression data, highlighting practical applicability.