Evidence map›Paper›PMID 30232133›Full record

ArticleJournal of clinical microbiology2018

Detection of Viruses in Clinical Samples by Use of Metagenomic Sequencing and Targeted Sequence Capture.

Kristine M Wylie, Todd N Wylie, Richard Buller, Brandi Herter, Maria T Cannella, Gregory A Storch

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 59 citations in OpenAlex.

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  12. The plasma virome in longitudinal samples from pregnant patients.Frontiers in cellular and infection microbiology · 2023
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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

6 authors at 2 institutions in 1 country.

Kristine M WylieDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA kwylie@wustl.edu.ORCID 0000-0002-2504-0661
Todd N WylieDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Richard BullerDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Brandi HerterDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Maria T CannellaDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Gregory A StorchDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Washington University in St. Louis · USJames S. McDonnell Foundation · US

Funding

DEFINING THE HUMAN VIROME IN IMMUNOCOMPROMISED CHILDRENR01AI097213 · NIAID · WASHINGTON UNIVERSITY · PI STORCH, GREGORY A. · 2012 to 2016
$3.2M
NIAID NIH HHS R01 AI097213
6 · The paper itself

Abstract

Metagenomic shotgun sequencing (MSS) is a revolutionary approach to viral diagnostic testing that allows simultaneous detection of a broad range of viruses, detailed taxonomic assignment, and detection of mutations associated with antiviral drug resistance. To enhance sensitivity for virus detection, we previously developed ViroCap, a targeted sequence capture panel designed to enrich nucleic acid from a comprehensive set of eukaryotic viruses prior to sequencing. To demonstrate the utility of MSS with targeted sequence capture for detecting clinically important viruses and characterizing clinically important viral features, we used ViroCap to analyze clinical samples from a diagnostic virology laboratory containing a broad range of medically relevant viruses. From 26 samples, MSS with ViroCap detected all of the expected viruses and 30 additional viruses. Comparing sequencing after capture enrichment with standard MSS, we detected 13 viruses only with capture enrichment and observed a consistent increase in the number and percentage of viral sequence reads as well as the breadth and depth of coverage of the viral genomes. Compared with clinical testing, MSS enhanced taxonomic assignment for 15 viruses, and codons associated with antiviral drug resistance in influenza A virus, herpes simplex virus (HSV), human immunodeficiency virus (HIV), and hepatitis C virus (HCV) could be analyzed. Overall, in clinical samples, MSS with targeted sequence capture provides enhanced virus detection and information of clinical and epidemiologic relevance compared with clinical testing and MSS without targeted sequence capture.

Indexed as

MetagenomicsDNA, ViralGenome, ViralHumansMolecular Diagnostic TechniquesRNA, ViralVirus DiseasesVirusesDNA, ViralRNA, Viraldiagnostic testingsequencingtargeted sequence capturevirology

Identifiers

PMID30232133
PMCPMC6258860
OpenAlexW2890665816

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.