Evidence map›Paper›PMID 27004841›Full record

ReviewBMC medicine2016

Clinical use of whole genome sequencing for Mycobacterium tuberculosis.

Adam A Witney, Catherine A Cosgrove, Amber Arnold, Jason Hinds, Neil G Stoker, Philip D Butcher

Open access · goldAbstract readReview
In one paragraph

Review in BMC medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
13.6field-weighted citation impact, top 1% of its field
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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 113 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Protein Architecture and Composition in Mycobacterium tuberculosis.Advances in experimental medicine and biology · 2026
    Review
  5. Article
  6. Review
  7. Advanced Therapeutic Interventions TargetingArchives of Razi Institute · 2025
    Review
  8. Review
  9. Article
  10. Characterizing the resistome ofFrontiers in microbiology · 2025
    Article
  11. Culture-Free Whole Genome Sequencing ofOpen forum infectious diseases · 2024
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Direct detection of drug-resistantFrontiers in public health · 2023
    Article
  19. Deciphering complex antibiotic resistance patterns inFrontiers in cellular and infection microbiology · 2023
    Article
  20. Review
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

6 authors at 2 institutions in 1 country.

Adam A WitneyInstitute of Infection and Immunity, St George's University of London, Cranmer Terrace, London, SW17 0RE, UK. awitney@sgul.ac.uk.
Catherine A CosgroveInstitute of Infection and Immunity, St George's University of London, Cranmer Terrace, London, SW17 0RE, UK.
Amber ArnoldClinical Infection Unit, St George's University Hospitals NHS Foundation Trust, Blackshaw Road, London, SW17 0QT, UK.
Jason HindsInstitute of Infection and Immunity, St George's University of London, Cranmer Terrace, London, SW17 0RE, UK.
Neil G StokerInstitute of Infection and Immunity, St George's University of London, Cranmer Terrace, London, SW17 0RE, UK.
Philip D ButcherInstitute of Infection and Immunity, St George's University of London, Cranmer Terrace, London, SW17 0RE, UK.
St George's, University of London · GBSt George’s University Hospitals NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drug-resistant tuberculosis (TB) remains a major challenge to global health and to healthcare in the UK. In 2014, a total of 6,520 cases of TB were recorded in England, of which 1.4 % were multidrug-resistant TB (MDR-TB). Extensively drug-resistant TB (XDR-TB) occurs at a much lower rate, but the impact on the patient and hospital is severe. Current diagnostic methods such as drug susceptibility testing and targeted molecular tests are slow to return or examine only a limited number of target regions, respectively. Faster, more comprehensive diagnostics will enable earlier use of the most appropriate drug regimen, thus improving patient outcomes and reducing overall healthcare costs. Whole genome sequencing (WGS) has been shown to provide a rapid and comprehensive view of the genotype of the organism, and thus enable reliable prediction of the drug susceptibility phenotype within a clinically relevant timeframe. In addition, it provides the highest resolution when investigating transmission events in possible outbreak scenarios. However, robust software and database tools need to be developed for the full potential to be realized in this specialized area of medicine.

Indexed as

Genome, BacterialAntitubercular AgentsExtensively Drug-Resistant TuberculosisHumansMicrobial Sensitivity TestsMycobacterium tuberculosisPolymorphism, GeneticSequence Analysis, DNATuberculosis, Multidrug-ResistantUnited KingdomAntitubercular AgentsMultidrug resistanceTuberculosisWhole genome sequencing

Identifiers

PMID27004841
PMCPMC4804576
OpenAlexW2305393516

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.