Analytical performance of norovirus real-time RT-PCR detection protocols in Canadian laboratories.

doi:10.1016/j.jcv.2010.10.008

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Analytical performance of norovirus real-time RT-PCR detection protocols in Canadian laboratories.

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology - 1 Feb 2011

Mattison Kirsten, Grudeski Elsie, Auk Brian, Brassard Julie, Charest Hugues, Dust Kerry, Gubbay Jonathan, Hatchette Todd F, Houde Alain, Jean Julie, Jones Tineke, Lee Bonita E, Mamiya Hiroshi, McDonald Ryan, Mykytczuk Oksana, Pang Xiaoli, Petrich Astrid, Plante Daniel, Ritchie Gordon, Wong Julie, Booth Tim F

Abstract excerpt

BACKGROUND: Noroviruses (NoVs) are the leading cause of infectious gastroenteritis worldwide. Real-time reverse transcription PCR (real-time RT-PCR) is the preferred method of NoV detection for the majority of testing laboratories. Although the accepted target region for molecular detection assays is the conserved ORF1/ORF2 junction, multiple variations have been published with differences in primers, probes,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Caliciviridae Infections

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Canada

Share to Feces

Share to Gastroenteritis

Share to Limit of Detection

Share to Norovirus

Share to Open Reading Frames

Share to RNA, Viral

Source

Open in PubMed

Identifiers

PMID: 21071266
DOI: 10.1016/j.jcv.2010.10.008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analytical performance of norovirus real-time RT-PCR detection protocols in Canadian laboratories.PMID 21071266Read ↗

Use of TaqMan Real-Time Reverse Transcription-PCR for Rapid Detection, Quantification, and Typing of NorovirusSemantic proximity Read ↗

Evaluation of Various Real-Time Reverse Transcription Quantitative PCR Assays for Norovirus DetectionSemantic proximity Read ↗

Molecular detection and genotyping of noroviruses.Semantic proximity Read ↗

Multiplex real-time RT-PCR for the simultaneous detection and quantification of GI, GII and GIV noroviruses.Semantic proximity Read ↗

Evaluation of real-time RT-PCR assays for detection and quantification of norovirus genogroups I and II.Semantic proximity Read ↗

Validation of a point-of-need diagnostic tool for rapid diagnosis of norovirus gastroenteritis.Semantic proximity Read ↗

Optimization of one-step real-time reverse transcription-polymerase chain reaction assays for norovirus detection and molecular epidemiology of noroviruses in ThailandSemantic proximity Read ↗

A comparison of the efficiency of ELISA and selected primer sets to detect Norovirus isolates in southern Ireland over a four-year period (2002-2006): variation in detection rates and evidence for continuing predominance of NoV GII.4 genotype.Semantic proximity Read ↗

Evaluation of the RIDAGENE real-time PCR assay for the detection of GI and GII norovirus.Semantic proximity Read ↗

High genetic variability of norovirus leads to diagnostic test challenges.Semantic proximity Read ↗

Environmental detection of genogroup I, II, and IV noroviruses by using a generic real-time reverse transcription-PCR assay.Semantic proximity Read ↗

Development of a real-time RT-PCR and Reverse Line probe Hybridisation assay for the routine detection and genotyping of Noroviruses in Ireland.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.