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

Receptor-Binding-Motif-Targeted Sanger Sequencing: a Quick and Cost-Effective Strategy for Molecular Surveillance of SARS-CoV-2 Variants.

Microbiology spectrum - 29 Jun 2022

Chaki Sankar Prasad, Kahl-McDonagh Melissa M, Neuman Benjamin W, Zuelke Kurt A

Abstract excerpt

Whole-genome sequencing (WGS) is the gold standard for characterizing the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome and identification of new variants. However, the cost involved and time needed for WGS prevent routine, rapid clinical use. This study aimed to develop a quick and cost-effective surveillance strategy for SARS-CoV-2 variants in saliva and nasal swab samples by spike protein...

Read the complete abstract on PubMed

Topics

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

Share to Cost-Benefit Analysis
Share to COVID-19

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Viral

Share to Mutation

Share to Pandemics

Share to SARS-CoV-2

Source

Open in PubMed Open full text

Identifiers

PMID: 35638906
DOI: 10.1128/spectrum.00665-22
PMCID: PMC9241651

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Receptor-Binding-Motif-Targeted Sanger Sequencing: a Quick and Cost-Effective Strategy for Molecular Surveillance of SARS-CoV-2 Variants.PMID 35638906Read ↗

Targeted Sanger sequencing to recover key mutations in SARS-CoV-2 variant genome assemblies produced by next-generation sequencing.Semantic proximity Read ↗

Identification of SARS-CoV-2 Variants of Concern Using Amplicon Next-Generation Sequencing.Semantic proximity Read ↗

PCR-Sequencing Approaches to Assess Informative Mutations in SARS-Cov-2 Spike (S) and ORF7, ORF8 and N Genes Characterizing Variants of Concern and Variants of InterestSemantic proximity Read ↗

Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations.Semantic proximity Read ↗

Use of Sanger protocols to identify variants of concern, key mutations and track evolution of SARS-CoV-2.Semantic proximity Read ↗

SpikeSeq: A rapid, cost efficient and simple method to identify SARS-CoV-2 variants of concern by Sanger sequencing part of the spike protein gene.Semantic proximity Read ↗

Digital PCR Discriminates between SARS-CoV-2 Omicron Variants and Immune Escape Mutations.Semantic proximity Read ↗

SARS-CoV-2 spike gene Sanger sequencing methodology to identify variants of concern.Semantic proximity Read ↗

SpikeID: Rapid and unbiased identification of SARS-CoV-2 variants by spike sequencing.Semantic proximity Read ↗

A rapid, cost efficient and simple method to identify current SARS-CoV-2 variants of concern by Sanger sequencing part of the spike protein geneSemantic proximity Read ↗

Molecular biology of SARS-CoV-2 and techniques of diagnosis and surveillance.Semantic proximity Read ↗

Unveiling Inter- and Intra-Patient Sequence Variability with a Multi-Sample Coronavirus Target Enrichment Approach.Semantic proximity Read ↗

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