Evidence map›Paper›PMID 34128695›Full record

ArticlemSystems2021

Predicting Antimicrobial Resistance Using Partial Genome Alignments.

D Aytan-Aktug, M Nguyen, P T L C Clausen, R L Stevens, F M Aarestrup, O Lund, J J Davis

Abstract read
In one paragraph

Article in mSystems, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. bioRxiv : the preprint server for biology · 2026
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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

7 authors.

D Aytan-AktugNational Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.
M NguyenConsortium for Advanced Science and Engineering, University of Chicago, Chicago, Illinois, USA.
P T L C ClausenNational Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.
R L StevensConsortium for Advanced Science and Engineering, University of Chicago, Chicago, Illinois, USA.
F M AarestrupNational Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.
O LundNational Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.
J J DavisConsortium for Advanced Science and Engineering, University of Chicago, Chicago, Illinois, USA.

Funding

BIOINFORMATICS RESOURCE CENTERS FOR INFECTIOUS DISEASES: SARS-CoV-2 ACTIVITIES75N93019C00076 · NIAID · UNIVERSITY OF CHICAGO · PI STEVENS, RICK · 2019 to 2023
$32.6M
DOD | Defense Advanced Research Projects Agency (DARPA) HR0011150042NIAID NIH HHS 75N93019C00076Novo Nordisk Fonden (NNF) NNF16OC0021856
6 · The paper itself

Abstract

Antimicrobial resistance (AMR) is an important global health threat that impacts millions of people worldwide each year. Developing methods that can detect and predict AMR phenotypes can help to mitigate the spread of AMR by informing clinical decision making and appropriate mitigation strategies. Many bioinformatic methods have been developed for predicting AMR phenotypes from whole-genome sequences and AMR genes, but recent studies have indicated that predictions can be made from incomplete genome sequence data. In order to more systematically understand this, we built random forest-based machine learning classifiers for predicting susceptible and resistant phenotypes for Klebsiella pneumoniae (1,640 strains), Mycobacterium tuberculosis (2,497 strains), and Salmonella enterica (1,981 strains). We started by building models from alignments that were based on a reference chromosome for each species. We then subsampled each chromosomal alignment and built models for the resulting subalignments, finding that very small regions, representing approximately 0.1 to 0.2% of the chromosome, are predictive. In K. pneumoniae, M. tuberculosis, and S. enterica, the subalignments are able to predict multiple AMR phenotypes with at least 70% accuracy, even though most do not encode an AMR-related function. We used these models to identify regions of the chromosome with high and low predictive signals. Finally, subalignments that retain high accuracy across larger phylogenetic distances were examined in greater detail, revealing genes and intergenic regions with potential links to AMR, virulence, transport, and survival under stress conditions.

Indexed as

AMRantimicrobial resistancemachine learningMLrandom forest

Identifiers

PMID34128695
PMCPMC8269213

What OpenQuestion holds

Textmetadata
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.