Evidence map›Paper›PMID 41896736›Full record

ArticleBMC microbiology2026

BaGPipe: an automated, reproducible, and flexible pipeline for bacterial genome-wide association studies.

Kuangyi Charles Wei, Beth Blane, Jacqueline Toussaint, Sandra Reuter, Michelle S Toleman, Mili Estee Torok, Sharon J Peacock, Ewan M Harrison, Dinesh Aggarwal, William Roberts-Sengier

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Kuangyi Charles WeiParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK. kw524@cam.ac.uk.
Beth BlaneParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Jacqueline ToussaintEuropean Bioinformatics Institute, Cambridge, UK.
Sandra ReuterMedical Center - University of Freiburg, Freiburg, Germany.
Michelle S TolemanCambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Mili Estee TorokDepartment of Medicine, University of Cambridge, Cambridge, UK.
Sharon J PeacockDepartment of Medicine, University of Cambridge, Cambridge, UK.
Ewan M HarrisonParasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
Dinesh Aggarwal *Parasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK.
William Roberts-Sengier *Parasites and Microbes Programme, Wellcome Sanger Institute, Hinxton, UK. wr7@sanger.ac.uk.

Funding

German Ministry of Education and Research 01KI2018Wellcome Trust 220540/Z/20/AWellcome Trust 222903/Z/21/Z
6 · The paper itself

Abstract

backgroundMicrobial genome-wide association studies (GWAS) are crucial for linking genetic variation to phenotypic traits in bacteria. However, current tools often involve complex manual processing, limited scalability, and fragmented workflows, which constrain large-scale or routine bacterial GWAS.

resultsWe developed BaGPipe, an automated and flexible bacterial GWAS pipeline built using Nextflow and incorporating Pyseer for association analysis. BaGPipe integrates pre-processing, statistical analysis, and downstream visualisation into a unified workflow that is reproducible and easy to deploy across diverse computational environments. BaGPipe was validated on a publicly available dataset of Streptococcus pneumoniae whole-genome sequences, and reproduced published findings with improved computational efficiency. BaGPipe was then applied to a dataset of Staphylococcus aureus whole-genome sequences, successfully identifying known and novel antibiotic resistance associations.

conclusionsBy offering an accessible, efficient, and reproducible platform, BaGPipe accelerates bacterial GWAS and facilitates deeper exploration into the genetic underpinnings of phenotypic traits. BaGPipe is freely available at https://github.com/sanger-pathogens/BaGPipe .

Indexed as

BacteriaComputational BiologyGenome, BacterialGenome-Wide Association StudySoftwarePhenotypeReproducibility of ResultsStaphylococcus aureusStreptococcus pneumoniaeWhole Genome SequencingGenome-wide association studyMicrobial GWASNextflow pipelinePyseerWhole genome sequencing

Identifiers

PMID41896736
PMCPMC13147680

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.