Evidence map›Paper›PMID 38954842›Full record

ArticleBioinformatics (Oxford, England)2024

DODGE: automated point source bacterial outbreak detection using cumulative long term genomic surveillance.

Michael Payne, Dalong Hu, Qinning Wang, Geraldine Sullivan, Rikki M Graham, Irani U Rathnayake, Amy V Jennison, Vitali Sintchenko, Ruiting Lan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. CharacterizingmSystems · 2025
    Article
  4. 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

9 authors.

Michael PayneSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.ORCID 0000-0003-1911-7033
Dalong HuSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.
Qinning WangCentre for Infectious Diseases and Microbiology-Public Health, Institute of Clinical Pathology and Medical Research-NSW Health Pathology, Westmead Hospital, Sydney, NSW 2145, Australia.
Geraldine SullivanCentre for Infectious Diseases and Microbiology-Public Health, Institute of Clinical Pathology and Medical Research-NSW Health Pathology, Westmead Hospital, Sydney, NSW 2145, Australia.
Rikki M GrahamPublic Health Microbiology, Queensland Health Forensic and Scientific Services, Coopers Plains, Brisbane, QLD 4108, Australia.
Irani U RathnayakePublic Health Microbiology, Queensland Health Forensic and Scientific Services, Coopers Plains, Brisbane, QLD 4108, Australia.
Amy V JennisonPublic Health Microbiology, Queensland Health Forensic and Scientific Services, Coopers Plains, Brisbane, QLD 4108, Australia.
Vitali SintchenkoCentre for Infectious Diseases and Microbiology-Public Health, Institute of Clinical Pathology and Medical Research-NSW Health Pathology, Westmead Hospital, Sydney, NSW 2145, Australia.
Ruiting LanSchool of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW 2052, Australia.ORCID 0000-0001-9834-5258

Funding

National Health and Medical Research Council of Australia 1146938
6 · The paper itself

Abstract

summaryThe reliable and timely recognition of outbreaks is a key component of public health surveillance for foodborne diseases. Whole genome sequencing (WGS) offers high resolution typing of foodborne bacterial pathogens and facilitates the accurate detection of outbreaks. This detection relies on grouping WGS data into clusters at an appropriate genetic threshold. However, methods and tools for selecting and adjusting such thresholds according to the required resolution of surveillance and epidemiological context are lacking. Here we present DODGE (Dynamic Outbreak Detection for Genomic Epidemiology), an algorithm to dynamically select and compare these genetic thresholds. DODGE can analyse expanding datasets over time and clusters that are predicted to correspond to outbreaks (or "investigation clusters") can be named with established genomic nomenclature systems to facilitate integrated analysis across jurisdictions. DODGE was tested in two real-world Salmonella genomic surveillance datasets of different duration, 2 months from Australia and 9 years from the United Kingdom. In both cases only a minority of isolates were identified as investigation clusters. Two known outbreaks in the United Kingdom dataset were detected by DODGE and were recognized at an earlier timepoint than the outbreaks were reported. These findings demonstrated the potential of the DODGE approach to improve the effectiveness and timeliness of genomic surveillance for foodborne diseases and the effectiveness of the algorithm developed. AVAILABILITY AND IMPLEMENTATION: DODGE is freely available at https://github.com/LanLab/dodge and can easily be installed using Conda.

Indexed as

AlgorithmsDisease OutbreaksFoodborne DiseasesGenome, BacterialAustraliaGenomicsHumansSalmonellaUnited KingdomWhole Genome Sequencing

Identifiers

PMID38954842
PMCPMC11244691

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LicenceCC BY
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Registered trials

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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.