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A Direct Approach to False Discovery Rates
Abstract
Summary: Multiple-hypothesis testing involves guarding against much more complicated errors than single-hypothesis testing. Whereas we typically control the type I error rate for a single-hypothesis test, a compound error rate is controlled for multiple-hypothesis tests. For example, controlling the false discovery rate FDR traditionally involves intricate sequential p-value rejection methods based on the observed data. Whereas a sequential p-value method fixes the error rate and estimates its corresponding rejection region, we propose the opposite approach—we fix the rejection region and then estimate its corresponding error rate. This new approach offers increased applicability, accuracy and power. We apply the methodology to both the positive false discovery rate pFDR and FDR, and provide evidence for its benefits. It is shown that pFDR is probably the quantity of interest over FDR. Also discussed is the calculation of the q-value, the pFDR analogue of the p-value, which eliminates the need to set the error rate beforehand as is traditionally done. Some simple numerical examples are presented that show that this new approach can yield an increase of over eight times in power compared with the Benjamini–Hochberg FDR method.
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“The 2982 MLG that contained over 100 genes were tested for enrichment or depletion in individuals with ACVD (218 ACVD cases and 187 controls) according to the non-parametric method, Wilcoxon rank-sum test, and controlled for multiple testing (q-value <0.05)55, 60.”
From The gut microbiome in atherosclerotic cardiovascular disease (2017) · cites this paper as [60]
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Joint analysis of SNP and gene expression data in genetic association studies of complex diseases
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Cortico-cortical feedback engages active dendrites in visual cortex
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Comparing connectomes across subjects and populations at different scales
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Profiling bacterial community in upper respiratory tracts
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Species comparison of liver proteomes reveals links to naked mole-rat longevity and human aging
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Genetic association analyses of PDYN polymorphisms with heroin and cocaine addiction
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Eating patterns and food intake of persons with type 1 diabetes within the T1D Exchange
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Metadata
- Authors
- Storey, J. D.
- Affiliations
- Stanford University (US)
- Corresponding author
- Storey, John D.
- ORCID
- Storey, John D.
- Venue
- Journal of the Royal Statistical Society Series B: Statistical Methodology
- Publisher
- Oxford University Press (OUP)
- Published
- 2002-08-01
- Volume
- 64
- Issue
- 3
- Pages
- 479-498
- ISSN
- 1369-7412 (ISSN-L)
- 1467-9868
- OpenAlex
- W2105381419
- Cited by
- 5,603
- References
- 12
- Citations by year
- 2026: 164 · 2025: 183 · 2024: 239 · 2023: 245 · 2022: 201 · 2021: 278 · 2020: 249 · 2019: 249 · 2018: 279 · 2017: 274 · 2016: 297 · 2015: 255 · 2014: 340 · 2013: 348 · 2012: 363
- FWCI
- 96.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of the Royal Statistical Society Series B (Statistical Methodology) (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Science Foundation
- Topics
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods in Clinical Trials
- Physical Sciences › Mathematics › Statistics and Probability › Statistical Methods and Inference
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
- Keywords
- false discovery rate, multiple comparisons, Q-value, Benjamini-Hochberg procedure, statistical power
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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