Evidence map›Paper›PMID 33028602›Full record

ArticleJournal of clinical microbiology2020

Sensitive Identification of Bacterial DNA in Clinical Specimens by Broad-Range 16S rRNA Gene Enrichment.

Sara Rassoulian Barrett, Noah G Hoffman, Christopher Rosenthal, Andrew Bryan, Desiree A Marshall, Joshua Lieberman, Alexander L Greninger, Vikas Peddu, Brad T Cookson, Stephen J Salipante

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Sara Rassoulian BarrettDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Noah G HoffmanDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Christopher RosenthalDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Andrew BryanDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Desiree A MarshallDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Joshua LiebermanDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Alexander L GreningerDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-7443-0527
Vikas PedduDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Brad T CooksonDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA.
Stephen J SalipanteDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, Washington, USA stevesal@uw.edu.ORCID 0000-0001-8355-6992
University of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The broad-range detection and identification of bacterial DNA from clinical specimens are a foundational approach in the practice of molecular microbiology. However, there are circumstances under which conventional testing may yield false-negative or otherwise uninterpretable results, including the presence of multiple bacterial templates or degraded nucleic acids. Here, we describe an alternative, next-generation sequencing approach for the broad range detection of bacterial DNA using broad-range 16S rRNA gene hybrid capture ("16S Capture"). The method is able to deconvolute multiple bacterial species present in a specimen, is compatible with highly fragmented templates, and can be readily implemented when the overwhelming majority of nucleic acids in a specimen derive from the human host. We find that this approach is sensitive to detecting as few as 17

Indexed as

MetagenomicsDNA, BacterialGenes, rRNAHumansRNA, Ribosomal, 16SSequence Analysis, DNADNA, BacterialRNA, Ribosomal, 16S16S rRNAbroad rangeenrichmenthybridization capturemetagenomicsmolecular diagnosisnext-generation sequencingsequencing

Identifiers

PMID33028602
PMCPMC7685877
OpenAlexW3092434199

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.