Evidence map›Paper›PMID 27535685›Full record

ArticleJournal of clinical microbiology2016

Comparative Performance of Reagents and Platforms for Quantitation of Cytomegalovirus DNA by Digital PCR.

R T Hayden, Z Gu, S S Sam, Y Sun, L Tang, S Pounds, A M Caliendo

Abstract readComparative StudyEvaluation Study
In one paragraph

Article in Journal of clinical microbiology, 2016. 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
–field-weighted citation impact
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.

  1. Review
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  10. Article
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  12. Article
  13. Absolute Enumeration of Probiotic StrainsFrontiers in microbiology · 2018
    Article
  14. Applications of Digital PCR for Clinical Microbiology.Journal of clinical microbiology · 2017
    Review
  15. 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

7 authors.

R T HaydenDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA Randall.Hayden@stjude.org.
Z GuDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
S S SamMiriam Hospital, Providence, Rhode Island, USA.
Y SunDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
L TangDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
S PoundsDepartment of Biostatistics, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
A M CaliendoDepartment of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A potential benefit of digital PCR is a reduction in result variability across assays and platforms. Three sets of PCR reagents were tested on two digital PCR systems (Bio-Rad and RainDance), using three different sets of PCR reagents for quantitation of cytomegalovirus (CMV). Both commercial quantitative viral standards and 16 patient samples (n = 16) were tested. Quantitative accuracy (compared to nominal values) and variability were determined based on viral standard testing results. Quantitative correlation and variability were assessed with pairwise comparisons across all reagent-platform combinations for clinical plasma sample results. The three reagent sets, when used to assay quantitative standards on the Bio-Rad system, all showed a high degree of accuracy, low variability, and close agreement with one another. When used on the RainDance system, one of the three reagent sets appeared to have a much better correlation to nominal values than did the other two. Quantitative results for patient samples showed good correlation in most pairwise comparisons, with some showing poorer correlations when testing samples with low viral loads. Digital PCR is a robust method for measuring CMV viral load. Some degree of result variation may be seen, depending on platform and reagents used; this variation appears to be greater in samples with low viral load values.

Indexed as

Indicators and ReagentsCytomegalovirusCytomegalovirus InfectionsDNA, ViralHumansPolymerase Chain ReactionReproducibility of ResultsViral LoadDNA, ViralIndicators and Reagents

Identifiers

PMID27535685
PMCPMC5035403

What OpenQuestion holds

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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.