Evidence map›Paper›PMID 39611092›Full record

ArticleFrontiers in microbiology2024

Comparison of three source attribution methods applied to whole genome sequencing data of monophasic and biphasic

Jaromir Guzinski, Mark Arnold, Tim Whiteley, Yue Tang, Virag Patel, Jahcub Trew, Eva Litrup, Tine Hald, Richard Piers Smith, Liljana Petrovska

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2024. 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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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Jaromir GuzinskiDepartment of Bacteriology, Animal and Plant Health Agency, Addlestone, United Kingdom.
Mark ArnoldDepartment of Epidemiological Sciences, Animal and Plant Health Agency, Addlestone, United Kingdom.
Tim WhiteleyDepartment of Epidemiological Sciences, Animal and Plant Health Agency, Addlestone, United Kingdom.
Yue TangDepartment of Bacteriology, Animal and Plant Health Agency, Addlestone, United Kingdom.
Virag PatelDepartment of Epidemiological Sciences, Animal and Plant Health Agency, Addlestone, United Kingdom.
Jahcub TrewDepartment of Bacteriology, Animal and Plant Health Agency, Addlestone, United Kingdom.
Eva LitrupFoodborne Infections, Department of Bacteria, Parasites and Fungi, Statens Serum Institute, Copenhagen, Denmark.
Tine HaldResearch Group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.
Richard Piers SmithDepartment of Epidemiological Sciences, Animal and Plant Health Agency, Addlestone, United Kingdom.
Liljana PetrovskaDepartment of Bacteriology, Animal and Plant Health Agency, Addlestone, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Methodologies for source attribution (SA) of foodborne illnesses comprise a rapidly expanding suite of techniques for estimating the most important source or sources of human infection. Recently, the increasing availability of whole genome sequencing (WGS) data for a wide range of bacterial strains has led to the development of novel SA methods. These techniques utilize the unique features of bacterial genomes adapted to different host types and hence offer increased resolution of the outputs. Comparative studies of different SA techniques reliant on WGS data are currently lacking. Here, we critically assessed and compared the outputs of three SA methods: a supervised classification random forest machine learning algorithm (RandomForest), an Accessory genes-Based Source Attribution method (AB_SA), and a Bayesian frequency matching method (Bayesian). Each technique was applied to the WGS data of a panel of 902 reservoir host and human monophasic and biphasic

Indexed as

Accessory genes-Based Source Attributionbacterial genomicsBayesian modelingmachine learningmonophasic and biphasic Salmonella Typhimuriumrandom forestsource attribution

Identifiers

PMID39611092
PMCPMC11602282

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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.