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.

PMID: 32502244
Funding: - NSFC: 31470675