Discover Community Create You

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

Article

Transcription-mediated amplification linked to line probe assay as a routine tool for HCV typing in clinical laboratories.

Journal of clinical laboratory analysis - 1 Jan 2007

Ross R S, Viazov S, Kpakiwa S S, Roggendorf M

Abstract excerpt

Typing of hepatitis C virus (HCV) isolates is currently a prerequisite for adequate tailoring of antiviral combination therapy. In many diagnostic laboratories, there seems to be a tendency toward convenient and time-saving procedures utilizing amplification products, which are already available from preceding qualitative or quantitative HCV ribonucleic acid (RNA) assays. In this context, we evaluated the...

Read the complete abstract on PubMed

Topics

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

Share to Aged, 80 and over
Share to Hepacivirus
Share to Hepatitis C

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Nucleic Acid Amplification Techniques

Share to Reverse Transcriptase Polymerase Chain Reaction

Share to RNA, Viral

Share to Sequence Alignment

Share to Sequence Analysis, RNA

Source

Open in PubMed Open full text

Identifiers

PMID: 17847116
DOI: 10.1002/jcla.20195
PMCID: PMC6648968

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Transcription-mediated amplification linked to line probe assay as a routine tool for HCV typing in clinical laboratories.PMID 17847116Read ↗

Genotyping of hepatitis C virus isolates by a new line probe assay using sequence information from both the 5'untranslated and the core regions.Semantic proximity Read ↗

Genotyping hepatitis C viruses from Southeast Asia by a novel line probe assay that simultaneously detects core and 5' untranslated regions.Semantic proximity Read ↗

Evaluation of a new-generation line-probe assay that detects 5' untranslated and core regions to genotype and subtype hepatitis C virus.Semantic proximity Read ↗

Comparison of line probe assay and DNA sequencing of 5' untranslated region for genotyping hepatitis C virus: description of novel line probe patterns.Semantic proximity Read ↗

Improvement of hepatitis C virus (HCV) genotype determination with the new version of the INNO-LiPA HCV assay.Semantic proximity Read ↗

Comparison of three different HCV genotyping methods: core, NS5B sequence analysis and line probe assay.Semantic proximity Read ↗

Clinical evaluation of a newly developed automated massively parallel sequencing assay for hepatitis C virus genotyping and detection of resistance-association variants. Comparison with a line probe assay.Semantic proximity Read ↗

[Investigation of Hepatitis C Virus (HCV) Genotypes by "Reverse Hybridisation Strip Assay" and DNA Sequence Analysis Methods].Semantic proximity Read ↗

Successful HCV genotyping of previously failed and low viral load specimens using an HCV RNA qualitative assay based on transcription-mediated amplification in conjunction with the line probe assay.Semantic proximity Read ↗

Analysis of hepatitis C virus genotypes by a line probe assay and correlation with antibody profiles.Semantic proximity Read ↗

Comparison of Abbott RealTime HCV Genotype II with Versant Line Probe Assay 2.0 for Hepatitis C Virus GenotypingSemantic proximity Read ↗

Clinical evaluation of two methods for genotyping hepatitis C virus based on analysis of the 5' noncoding region.Semantic proximity Read ↗

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