Performing highly parallelized and reproducible GWAS analysis on biobank-scale data.


Journal

NAR genomics and bioinformatics
ISSN: 2631-9268
Titre abrégé: NAR Genom Bioinform
Pays: England
ID NLM: 101756213

Informations de publication

Date de publication:
Mar 2024
Historique:
received: 05 10 2023
revised: 21 12 2023
accepted: 24 01 2024
medline: 8 2 2024
pubmed: 8 2 2024
entrez: 8 2 2024
Statut: epublish

Résumé

Genome-wide association studies (GWAS) are transforming genetic research and enable the detection of novel genotype-phenotype relationships. In the last two decades, over 60 000 genetic associations across thousands of traits have been discovered using a GWAS approach. Due to increasing sample sizes, researchers are increasingly faced with computational challenges. A reproducible, modular and extensible pipeline with a focus on parallelization is essential to simplify data analysis and to allow researchers to devote their time to other essential tasks. Here we present nf-gwas, a Nextflow pipeline to run biobank-scale GWAS analysis. The pipeline automatically performs numerous pre- and post-processing steps, integrates regression modeling from the REGENIE package and supports single-variant, gene-based and interaction testing. It includes an extensive reporting functionality that allows to inspect thousands of phenotypes and navigate interactive Manhattan plots directly in the web browser. The pipeline is tested using the unit-style testing framework nf-test, a crucial requirement in clinical and pharmaceutical settings. Furthermore, we validated the pipeline against published GWAS datasets and benchmarked the pipeline on high-performance computing and cloud infrastructures to provide cost estimations to end users. nf-gwas is a highly parallelized, scalable and well-tested Nextflow pipeline to perform GWAS analysis in a reproducible manner.

Identifiants

pubmed: 38327871
doi: 10.1093/nargab/lqae015
pii: lqae015
pmc: PMC10849172
doi:

Types de publication

Journal Article

Langues

eng

Pagination

lqae015

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics.

Auteurs

Sebastian Schönherr (S)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.

Johanna F Schachtl-Riess (JF)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.

Silvia Di Maio (S)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.

Michele Filosi (M)

Institute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, Italy. Institutional Address: Via Alessandro Volta, 21, 39100 Bolzano BZ, Italy.

Marvin Mark (M)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.

Claudia Lamina (C)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.

Christian Fuchsberger (C)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.
Institute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, Italy. Institutional Address: Via Alessandro Volta, 21, 39100 Bolzano BZ, Italy.

Florian Kronenberg (F)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.

Lukas Forer (L)

Institute of Genetic Epidemiology, Medical University of Innsbruck, Innsbruck, Austria. Institutional Address: Schoepfstrasse 41, A-6020 Innsbruck, Austria.

Classifications MeSH