Eagle

Eagle performs multi-locus association mapping on genome-wide genotype-phenotype data to detect SNP-trait associations using model selection, linear mixed models, and random effects.


Key Features:

  • R implementation: Provided as an R package for computational analysis of genetic association data.
  • Multi-locus association mapping: Tests associations across multiple loci genome-wide rather than relying on single-locus tests.
  • Linear mixed models: Applies linear mixed models to account for population structure and relatedness among individuals.
  • Model selection: Integrates model selection techniques to identify significant SNP-trait associations.
  • Random effects modeling: Incorporates random effects to capture additional genetic variance and refine association signals.
  • Enhanced detection power: Improves detection of SNP-trait associations compared to conventional single-locus methods.
  • GWAS scale: Designed for genome-wide association study (GWAS) analyses.

Scientific Applications:

  • Genome-wide association studies (GWAS): Identification of SNP-trait associations while accounting for confounding due to structure and relatedness.
  • Complex trait mapping: Detection of multi-locus genetic interactions and subtle genetic influences on phenotypes.
  • Mouse genetics: Analysis of real mouse genotype-phenotype datasets to refine and extend single-locus findings.
  • Refinement of single-locus results: Complementing single-locus analyses by identifying additional loci and interactions.

Methodology:

Eagle integrates model selection with linear mixed models and random-effects modeling to account for population structure and relatedness when identifying significant SNP-trait associations.

Topics

Details

License:
GPL-3.0
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R
Added:
2/24/2022
Last Updated:
2/24/2022

Operations

Publications

George AW, Verbyla A, Bowden J. Eagle for better genome-wide association mapping. G3 Genes|Genomes|Genetics. 2021;11(9). doi:10.1093/g3journal/jkab204. PMID:34544142. PMCID:PMC8496271.

Links