GWAR
GWAR implements robust statistical tests and meta-analysis procedures for genome-wide association studies (GWAS) to maximize analytical power while maintaining nominal type I error rates.
Key Features:
- Robust statistical tests: Implements the Cochran-Armitage trend test (CATT) under recessive, additive, and dominant genetic models, the Maximum Efficiency Robust Test statistic (MAX), and the MIN2 statistic.
- Asymptotic null distributions: Computes asymptotic null distributions for the MAX and MIN2 statistics using numerical integration to improve computational efficiency and accuracy.
- Type I error control: Maintains nominal type I error rates while maximizing analytical power in association testing.
- Meta-analysis capabilities: Performs fixed- and random-effects meta-analysis on summary data with weights equal to the reciprocal of combined cases and controls.
- Stata implementation: Implemented as a program within the Stata environment.
Scientific Applications:
- Association testing under model uncertainty: Detects genetic associations when the underlying genetic model (recessive, additive, or dominant) is unknown.
- GWAS meta-analysis: Synthesizes summary data across multiple studies using fixed- and random-effects models to increase statistical power and generalizability.
- Control of false positives: Provides analyses that preserve nominal type I error rates in genome-wide association studies.
Methodology:
Implements CATT (recessive, additive, dominant), MAX and MIN2 statistics, derives asymptotic null distributions for MAX and MIN2 via numerical integration, and supports fixed- and random-effects meta-analysis using summary-data weights equal to the reciprocal of combined cases and controls.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 7/27/2017
- Last Updated:
- 11/25/2024
Operations
Publications
Dimou NL, Tsirigos KD, Elofsson A, Bagos PG. GWAR: robust analysis and meta-analysis of genome-wide association studies. Bioinformatics. 2017;33(10):1521-1527. doi:10.1093/bioinformatics/btx008. PMID:28108451.
PMID: 28108451