HiGwas
HiGwas performs longitudinal genome-wide association analyses to integrate longitudinal phenotypic data with high-dimensional single-nucleotide polymorphism (SNP) genotypes and identify additive and dominant genetic effects in "big p, small n" GWAS settings.
Key Features:
- Longitudinal Data Integration: Integrates longitudinal phenotypic data to capture temporal variation in traits that single-time-point measurements may miss.
- Statistical Models: Implements dimension reduction methods and longitudinal data analysis techniques that handle the autocorrelative nature of repeated measures.
- Single-SNP and High-Dimensional SNP-Set Handling: Performs single SNP analyses and high-dimensional SNP-set handling including significance-level adjustment, preconditioning, and model selection.
- Estimation of Genetic Parameters: Provides estimates of genetic parameters with confidence intervals for additive and dominant effects.
Scientific Applications:
- Functional Genomics and Complex Trait Genetics: Facilitates investigation of genetic architectures underlying complex traits using longitudinal GWAS data.
- Longitudinal Disease Studies: Supports analysis of diseases with progressive or fluctuating courses, such as cardiovascular diseases, diabetes, and neurodegenerative disorders, by linking genetic variation to phenotypic change over time.
Methodology:
Implements dimension reduction methods and longitudinal data analysis techniques that account for autocorrelation, performs single-SNP analyses and high-dimensional SNP-set handling with significance-level adjustment, preconditioning, and model selection, and estimates genetic parameters (additive and dominant effects) with confidence intervals.
Topics
Details
- Tool Type:
- command-line tool
- Programming Languages:
- C++, R, C
- Added:
- 1/18/2021
- Last Updated:
- 1/30/2021
Operations
Publications
Wang Z, Wang N, Wang Z, Jiang L, Wang Y, Li J, Wu R. <i>HiG</i>was: how to compute longitudinal GWAS data in population designs. Bioinformatics. 2020;36(14):4222-4224. doi:10.1093/bioinformatics/btaa294. PMID:32502244.