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

A Sanger-based approach for scaling up screening of SARS-CoV-2 variants of interest and concern.

Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases - 1 Aug 2021

Bezerra Matheus Filgueira, Machado Lais Ceschini, De Carvalho Viviane do Carmo Vasconcelos, Docena Cássia, Brandão-Filho Sinval Pinto, Ayres Constância Flávia Junqueira, Paiva Marcelo Henrique Santos, Wallau Gabriel Luz

Abstract excerpt

The global spread of new SARS-CoV-2 variants of concern underscore an urgent need of simple deployed molecular tools that can differentiate these lineages. Several tools and protocols have been shared since the beginning of the COVID-19 pandemic, but they need to be timely adapted to cope with SARS-CoV-2 evolution. Although whole-genome sequencing (WGS) of the virus genetic material has been widely used, it still...

Read the complete abstract on PubMed

Topics

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

Share to COVID-19
Share to CRISPR and Genetic Engineering

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Regulation, Viral

Share to Genetic Variation

Share to Reproducibility of Results

Share to SARS-CoV-2

Share to SARS-CoV-2 and COVID-19 Research

Share to Viral Proteins

Source

Open in PubMed Open full text

Identifiers

PMID: 33975021
DOI: 10.1016/j.meegid.2021.104910
PMCID: PMC8105304

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

A Sanger-based approach for scaling up screening of SARS-CoV-2 variants of interest and concern.PMID 33975021Read ↗

A Sanger-based approach for scaling up screening of SARS-CoV-2 variants of interest and concernSemantic proximity Read ↗

Survey of SARS-CoV-2 genetic diversity in two major Brazilian cities using a fast and affordable Sanger sequencing strategy.Semantic proximity Read ↗

Survey of SARS-CoV-2 genetic diversity in two major Brazilian cities using a fast and affordable Sanger sequencing strategySemantic proximity Read ↗

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

A Rapid and Consistent Method To Identify SARS-CoV-2 Variants By RT-PCRSemantic proximity Read ↗

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 ↗

Rapid System to Detect the Main Variants of SARS-CoV-2 in Biological SpecimensSemantic proximity Read ↗

Epidemic Spread of SARS-CoV-2 Lineage B.1.1.7 in BrazilSemantic proximity Read ↗

Genomic monitoring unveil the early detection of the SARS-CoV-2 B.1.351 (beta) variant (20H/501Y.V2) in Brazil.Semantic proximity Read ↗

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