Evidence map›Paper›PMID 36000741›Full record

ArticlemSphere2022

Comparison of Metagenomic Sequencing and the NanoString nCounter Analysis System for the Characterization of Bacterial and Viral Communities in Vaginal Samples.

Todd N Wylie, Jane Schrimpf, Haley Gula, Brandi N Herter, Kristine M Wylie

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 46% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
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

5 authors at 2 institutions in 1 country.

Todd N Wylie *Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID 0000-0001-8834-8404
Jane Schrimpf *Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Haley GulaDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Brandi N HerterDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.
Kristine M WylieDepartment of Pediatrics, Washington University School of Medicine, St. Louis, Missouri, USA.ORCID 0000-0002-2504-0661
Washington University in St. Louis · USJames S. McDonnell Foundation · US

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Rapid Characterization of the Vaginal Microbiome/Virome in Pregnant WomenR03AI159038 · NIAID · WASHINGTON UNIVERSITY · PI WYLIE, KRISTINE M. · 2021 to 2022
$158k
NCATS NIH HHS UL1 TR002345NIAID NIH HHS R03 AI159038
6 · The paper itself

Abstract

DNA sequencing assays have been used to characterize the vaginal microbiome and to identify associations with clinical outcomes. The purpose of this study was to evaluate the utility of the NanoString nCounter platform, a more efficient assay compared to sequencing, for the characterization of vaginal microbial communities. A panel of NanoString nCounter probes was designed to detect common vaginal bacteria and viruses with relevance to reproductive health. A defined synthetic community of microbes and 43 clinical samples were interrogated with NanoString nCounter assays and compared to known compositions or metagenomic shotgun sequencing (MSS) results. The NanoString nCounter platform and MSS were able to distinguish closely related microbes. In clinical samples, the relative abundance of bacterial species was similar between the two assays. The assays sometimes disagreed when targets were present at low abundance. More viruses were detected by MSS than by nCounter. However, the nCounter assays are able to provide results in about 30 h with minimal hands-on time, whereas MSS requires at least 138 to 178 h with extensive hands-on time. The reagent cost for the two assays was similar, but the overall cost of the nCounter was lower due to the minimal hands-on time. MSS can be used to inform the design of a targeted multiplex panel for the assessment of vaginal microbial communities, thereby allowing for more cost-effective and rapid screening of patient samples for research studies. The sensitivity for low abundance microbes could be improved, possibly by adding additional target amplification cycles before nCounter assessment. This approach has potential as an assay with both research and clinical applications.

Indexed as

MetagenomicsVirusesBacteriaFemaleHumansMetagenomeSequence Analysis, DNAmicrobiomeNanoString nCountersequencingvaginavirome

Identifiers

PMID36000741
PMCPMC9599496
OpenAlexW4293212224

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.