Evidence map›Paper›PMID 37620118›Full record

ArticleGenome research2023

Accurate and fast graph-based pangenome annotation and clustering with ggCaller.

Samuel T Horsfield, Gerry Tonkin-Hill, Nicholas J Croucher, John A Lees

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. RefiningMicrobial genomics · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Pangenomics in the Mimulus guttatus Species Complex.Molecular ecology resources · 2026
    Article
  8. Article
  9. Article
  10. Pathogenomic Insights intoAnimals : an open access journal from MDPI · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Beyond H37Rv:Frontiers in microbiology · 2025
    Review
  15. Article
  16. Genomic Characterization ofMicroorganisms · 2024
    Article
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Samuel T HorsfieldMRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London W12 0BZ, United Kingdom; s.horsfield19@imperial.ac.uk.ORCID 0000-0002-3859-4073
Gerry Tonkin-HillDepartment of Biostatistics, University of Oslo, Blindern, 0372 Oslo, Norway.ORCID 0000-0003-4397-2224
Nicholas J Croucher *MRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London W12 0BZ, United Kingdom.ORCID 0000-0001-6303-8768
John A Lees *MRC Centre for Global Infectious Disease Analysis, Department of Infectious Disease Epidemiology, Imperial College London, London W12 0BZ, United Kingdom.ORCID 0000-0001-5360-1254
European Bioinformatics Institute · GBLondon Centre for Neglected Tropical Disease Research · GBUniversity of Oslo · NO

Funding

Medical Research Council MR/R015600/1Medical Research Council MR/S502388/1Medical Research Council MR/T016434/1Medical Research Council MR/X020258/1Wellcome TrustWellcome Trust 104169/Z/14/A
6 · The paper itself

Abstract

Bacterial genomes differ in both gene content and sequence mutations, which underlie extensive phenotypic diversity, including variation in susceptibility to antimicrobials or vaccine-induced immunity. To identify and quantify important variants, all genes within a population must be predicted, functionally annotated, and clustered, representing the "pangenome." Despite the volume of genome data available, gene prediction and annotation are currently conducted in isolation on individual genomes, which is computationally inefficient and frequently inconsistent across genomes. Here, we introduce the open-source software graph-gene-caller (ggCaller). ggCaller combines gene prediction, functional annotation, and clustering into a single workflow using population-wide de Bruijn graphs, removing redundancy in gene annotation and resulting in more accurate gene predictions and orthologue clustering. We applied ggCaller to simulated and real-world bacterial data sets containing hundreds or thousands of genomes, comparing it to current state-of-the-art tools. ggCaller has considerable speed-ups with equivalent or greater accuracy, particularly with data sets containing complex sources of error, such as assembly contamination or fragmentation. ggCaller is also an important extension to bacterial genome-wide association studies, enabling querying of annotated graphs for functional analyses. We highlight this application by functionally annotating DNA sequences with significant associations to tetracycline and macrolide resistance in

Indexed as

Anti-Bacterial AgentsGenome-Wide Association StudyAlgorithmsCluster AnalysisDrug Resistance, BacterialGenome, BacterialMacrolidesMolecular Sequence AnnotationSoftwareAnti-Bacterial AgentsMacrolides

Identifiers

PMID37620118
PMCPMC10620059
OpenAlexW4386122263

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.