Evidence map›Paper›PMID 24699691›Full record

ArticlePloS one2014

Deep sequencing to identify the causes of viral encephalitis.

Benjamin K Chan, Theodore Wilson, Kael F Fischer, John D Kriesel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
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  6. Article
  7. Review
  8. High-throughput sequencing for the aetiologic identification of viral encephalitis, meningoencephalitis, and meningitis. A narrative review and clinical appraisal.Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases · 2019
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Aseptic central nervous system infections in adults: what predictor for unknown etiological diagnosis?Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2018
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. MicroRNA-125b in peripheral blood: a potential biomarker for severity and prognosis of children with viral encephalitis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2017
    Article
  19. Application of next generation sequencing for the detection of human viral pathogens in clinical specimens.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2017
    Article
  20. 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

4 authors at 1 institution in 1 country.

Benjamin K ChanDivision of Infectious Diseases, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
Theodore WilsonDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
Kael F FischerDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
John D KrieselDivision of Infectious Diseases, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
University of Utah · US

Funding

Deep Sequencing for the Detection of Viral Sequences in Primary Progressive MultiR21NS077023 · NINDS · UNIVERSITY OF UTAH · PI KRIESEL, JOHN D · 2011 to 2012
$411k
NINDS NIH HHS R21 NS077023NINDS NIH HHS R21NS077023
6 · The paper itself

Abstract

Deep sequencing allows for a rapid, accurate characterization of microbial DNA and RNA sequences in many types of samples. Deep sequencing (also called next generation sequencing or NGS) is being developed to assist with the diagnosis of a wide variety of infectious diseases. In this study, seven frozen brain samples from deceased subjects with recent encephalitis were investigated. RNA from each sample was extracted, randomly reverse transcribed and sequenced. The sequence analysis was performed in a blinded fashion and confirmed with pathogen-specific PCR. This analysis successfully identified measles virus sequences in two brain samples and herpes simplex virus type-1 sequences in three brain samples. No pathogen was identified in the other two brain specimens. These results were concordant with pathogen-specific PCR and partially concordant with prior neuropathological examinations, demonstrating that deep sequencing can accurately identify viral infections in frozen brain tissue.

Indexed as

High-Throughput Nucleotide SequencingBrainEncephalitis, ViralHerpes SimplexHerpesvirus 1, HumanHumansMeaslesMeasles virusRNA, ViralRNA, Viral

Identifiers

PMID24699691
PMCPMC3974838
OpenAlexW1970342753

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.