Evidence map›Paper›PMID 29960078›Full record

ArticleInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases2019

Towards better prediction of Mycobacterium tuberculosis lineages from MIRU-VNTR data.

Nithum Thain, Christopher Le, Aldo Crossa, Shama Desai Ahuja, Jeanne Sullivan Meissner, Barun Mathema, Barry Kreiswirth, Natalia Kurepina, Ted Cohen, Leonid Chindelevitch

Abstract read
In one paragraph

Article in Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 2019. 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. Genotyping and drug susceptibility testing ofNew microbes and new infections · 2020
    Article
  3. 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

10 authors.

Nithum ThainSchool of Computing Science, Simon Fraser University, Burnaby, BC, Canada.
Christopher LeSchool of Computing Science, Simon Fraser University, Burnaby, BC, Canada.
Aldo CrossaNew York City Department of Health and Mental Hygiene, Queens, NY, USA.
Shama Desai AhujaNew York City Department of Health and Mental Hygiene, Queens, NY, USA.
Jeanne Sullivan MeissnerNew York City Department of Health and Mental Hygiene, Queens, NY, USA.
Barun MathemaDepartment of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.
Barry KreiswirthPublic Health Research Institute TB Center, Rutgers University, Newark, NJ, USA.
Natalia KurepinaPublic Health Research Institute TB Center, Rutgers University, Newark, NJ, USA.
Ted CohenEpidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
Leonid ChindelevitchSchool of Computing Science, Simon Fraser University, Burnaby, BC, Canada. Electronic address: leonid@sfu.ca.

Funding

Understanding and controlling antibiotic resistanceU54GM088558 · NIGMS · HARVARD SCHOOL OF PUBLIC HEALTH · PI HANAGE, WILLIAM · 2009 to 2018
$26.4M
NIGMS NIH HHS U54 GM088558
6 · The paper itself

Abstract

The determination of lineages from strain-based molecular genotyping information is an important problem in tuberculosis. Mycobacterial interspersed repetitive unit-variable number tandem repeat (MIRU-VNTR) typing is a commonly used molecular genotyping approach that uses counts of the number of times pre-specified loci repeat in a strain. There are three main approaches for determining lineage based on MIRU-VNTR data - one based on a direct comparison to the strains in a curated database, and two others, on machine learning algorithms trained on a large collection of labeled data. All existing methods have limitations. The direct approach imposes an arbitrary threshold on how much a database strain can differ from a given one to be informative. On the other hand, the machine learning-based approaches require a substantial amount of labeled data. Notably, all three methods exhibit suboptimal classification accuracy without additional data. We explore several computational approaches to address these limitations. First, we show that eliminating the arbitrary threshold improves the performance of the direct approach. Second, we introduce RuleTB, an alternative direct method that proposes a concise set of rules for determining lineages. Lastly, we propose StackTB, a machine learning approach that requires only a fraction of the training data to outperform the accuracy of both existing machine learning methods. Our approaches demonstrate superior performance on a training dataset collected in New York City over 10 years, and the improvement in performance translates to a held-out testing set. We conclude that our methods provide opportunities for improving the determination of pathogenic lineages based on MIRU-VNTR data.

Indexed as

Machine LearningComputational BiologyDatabases, Nucleic AcidGenetic VariationHumansInterspersed Repetitive SequencesMinisatellite RepeatsMolecular EpidemiologyMycobacterium tuberculosisNew York CityPhylogenyTuberculosisInterpretabilityLineageMachine learningMIRU-VNTRMycobacterium tuberculosis

Identifiers

PMID29960078
PMCPMC6708508

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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.