Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Nov 1;39(11):btad656.
doi: 10.1093/bioinformatics/btad656.

Expanded utility of the R package, qgg, with applications within genomic medicine

Affiliations

Expanded utility of the R package, qgg, with applications within genomic medicine

Palle Duun Rohde et al. Bioinformatics. .

Abstract

Summary: Here, we present an expanded utility of the R package qgg for genetic analyses of complex traits and diseases. One of the major updates of the package is, that it now includes Bayesian linear regression modeling procedures, which provide a unified framework for mapping of genetic variants, estimation of heritability and genomic prediction from either individual level data or from genome-wide association study summary data. With this release, the qgg package now provides a wealth of the commonly used methods in analysis of complex traits and diseases, without the need to switch between software and data formats.

Availability and implementation: The methodologies are implemented in the publicly available R software package, qgg, using fast and memory efficient algorithms in C++ and is available on CRAN or as a developer version at our GitHub page (https://github.com/psoerensen/qgg). Notes on the implemented statistical genetic models, tutorials and example scripts are available at our GitHub page https://psoerensen.github.io/qgg/.

PubMed Disclaimer

Conflict of interest statement

None declared.

Figures

Figure 1.
Figure 1.
Overview of the simple and streamlined workflow for genetic analysis of complex traits that takes PLINK files as input. The output from each function is designed to match the input format of downstream analyses.

References

    1. Bycroft C, Freeman C, Petkova D. et al. The UK Biobank resource with deep phenotyping and genomic data. Nature 2018;562:203–9. - PMC - PubMed
    1. Chang CC, Chow CC, Tellier LC. et al. Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience 2015;4:7–16. - PMC - PubMed
    1. Ehsani A, Janss L, Pomp D. et al. Decomposing genomic variance using information from GWA, GWE and eQTL analysis. Anim Genet 2016;47:165–73. - PubMed
    1. Ehsani A, Sørensen P, Pomp D. et al. Inferring genetic architecture of complex traits using Bayesian integrative analysis of genome and transcriptome data. BMC Genomics 2012;13:456. - PMC - PubMed
    1. Euesden J, Lewis CM, O'Reilly PF. et al. PRSice: polygenic risk score software. Bioinformatics 2015;31:1466–8. - PMC - PubMed

Publication types