TY - JOUR
T1 - GCPBayes
T2 - An R package for studying Cross-Phenotype Genetic Associations with Group-level Bayesian Meta-Analysis
AU - Baghfalaki, Taban
AU - Sugier, Pierre-Emmanuel
AU - Asgari, Yazdan
AU - Truong, Thérèse
AU - Liquet, Benoit
PY - 2023/3
Y1 - 2023/3
N2 - Several R packages have been developed to study cross-phenotypes associations (or pleiotropy) at the SNP-level, based on summary statistics data from genome-wide association studies (GWAS). However, none of them allow for consideration of the underlying group structure of the data. We developed an R package, entitled GCPBayes (Group level Bayesian Meta-Analysis for Studying Cross-Phenotype Genetic Associations), introduced by Baghfalaki et al. (2021), that implements continuous and Dirac spike priors for group selection, and also a Bayesian sparse group selection approach with hierarchical spike and slab priors, to select important variables at the group level and within the groups. The methods use summary statistics data from association studies or individual level data as inputs, and perform Bayesian meta-analysis approaches across multiple phenotypes to detect pleiotropy at both group-level (e.g., at the gene or pathway level) and within group (e.g., at the SNP level).
AB - Several R packages have been developed to study cross-phenotypes associations (or pleiotropy) at the SNP-level, based on summary statistics data from genome-wide association studies (GWAS). However, none of them allow for consideration of the underlying group structure of the data. We developed an R package, entitled GCPBayes (Group level Bayesian Meta-Analysis for Studying Cross-Phenotype Genetic Associations), introduced by Baghfalaki et al. (2021), that implements continuous and Dirac spike priors for group selection, and also a Bayesian sparse group selection approach with hierarchical spike and slab priors, to select important variables at the group level and within the groups. The methods use summary statistics data from association studies or individual level data as inputs, and perform Bayesian meta-analysis approaches across multiple phenotypes to detect pleiotropy at both group-level (e.g., at the gene or pathway level) and within group (e.g., at the SNP level).
UR - http://www.scopus.com/inward/record.url?scp=85172908160&partnerID=8YFLogxK
UR - https://journal.r-project.org/articles/RJ-2023-028/
U2 - 10.32614/RJ-2023-028
DO - 10.32614/RJ-2023-028
M3 - Article
AN - SCOPUS:85172908160
SN - 2073-4859
VL - 15
SP - 122
EP - 141
JO - R Journal
JF - R Journal
IS - 1
ER -