weighted_FDR
weighted_FDR applies a weighted false discovery rate to multiple hypothesis testing to increase statistical power for detecting genetic associations in genome-wide association studies and association genome scans.
Key Features:
- Multiple Testing Problem: Addresses loss of power from stringent corrections such as Bonferroni when hundreds of thousands of polymorphisms are tested.
- False Discovery Rate (FDR) Principle: Leverages FDR control to balance type I error control with higher statistical power compared to traditional methods.
- Weighted Hypotheses: Allows hypotheses to be weighted using prior data, for example from previous linkage scans, to enhance detection of modest genetic effects.
- Linkage Data Utilization: Uses linkage data to assign weights to association P values, integrating prior information into association testing.
- Power Improvement: Demonstrates substantial power gains when linkage studies are informative and minimal power loss when linkage information is limited.
- Sample Size Calculation: Provides a framework to calculate the sample size needed to obtain useful prior information from linkage studies.
Scientific Applications:
- Genome-wide association studies (GWAS): Improves detection of associations between genetic markers and complex diseases by managing the multiple testing burden.
- Association genome scans: Enables exploration of genomic regions with greater confidence even when prior evidence from linkage studies is weak.
Methodology:
Implements a weighted FDR procedure for multiple hypothesis testing that assigns weights to association P values using linkage data and includes a sample size calculation framework for obtaining prior information from linkage studies.
Topics
Details
- Tool Type:
- library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- R
- Added:
- 8/3/2017
- Last Updated:
- 11/24/2024
Operations
Publications
Roeder K, Bacanu S, Wasserman L, Devlin B. Using Linkage Genome Scans to Improve Power of Association in Genome Scans. The American Journal of Human Genetics. 2006;78(2):243-252. doi:10.1086/500026. PMID:16400608. PMCID:PMC1380233.
DOI: 10.1086/500026
PMID: 16400608
PMCID: PMC1380233
Funding: - National Institutes of Health: MH057881