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.

PMID: 16400608
PMCID: PMC1380233
Funding: - National Institutes of Health: MH057881

Documentation

Links