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 rapid, cost-effective tailed amplicon method for sequencing SARS-CoV-2.

BMC genomics - 4 Dec 2020

Gohl Daryl M, Garbe John, Grady Patrick, Daniel Jerry, Watson Ray H B, Auch Benjamin, Nelson Andrew, Yohe Sophia, Beckman Kenneth B

Abstract excerpt

BACKGROUND: The global COVID-19 pandemic has led to an urgent need for scalable methods for clinical diagnostics and viral tracking. Next generation sequencing technologies have enabled large-scale genomic surveillance of SARS-CoV-2 as thousands of isolates are being sequenced around the world and deposited in public data repositories. A number of methods using both short- and long-read technologies are currently...

Read the complete abstract on PubMed

Topics

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

Share to Benchmarking
Share to COVID-19
Share to Genome, Viral

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Molecular Epidemiology

Share to Mutation

Share to RNA, Viral

Share to SARS-CoV-2

Share to Sequence Analysis

Source

Open in PubMed Open full text

Identifiers

PMID: 33276717
DOI: 10.1186/s12864-020-07283-6
PMCID: PMC7716288

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A rapid, cost-effective tailed amplicon method for sequencing SARS-CoV-2.PMID 33276717Read ↗

A Rapid, Cost-Effective Tailed Amplicon Method for Sequencing SARS-CoV-2Semantic proximity Read ↗

Evaluation of NGS-based approaches for SARS-CoV-2 whole genome characterisationSemantic proximity Read ↗

Rapid and Inexpensive Whole-Genome Sequencing of SARS-CoV-2 using 1200 bp Tiled Amplicons and Oxford Nanopore Rapid BarcodingSemantic proximity Read ↗

Development and Validation of a High-Throughput Next-Generation Sequencing Workflow for SARS-CoV-2 Whole Genome Sequencing: Results from Over 65,000 Clinical CasesSemantic proximity Read ↗

Performance of amplicon and capture based next-generation sequencing approaches for the epidemiological surveillance of Omicron SARS-CoV-2 and other variants of concern.Semantic proximity Read ↗

Performance of amplicon and capture based next-generation sequencing approaches for the epidemiological surveillance of Omicron SARS-CoV-2 and other variants of concernSemantic proximity Read ↗

Evaluation of NGS-based approaches for SARS-CoV-2 whole genome characterisationSemantic proximity Read ↗

Detection of SARS-CoV-2 in saliva using tailed amplicon sequencingSemantic proximity Read ↗

A comparison of five Illumina, Ion Torrent, and nanopore sequencing technology-based approaches for whole genome sequencing of SARS-CoV-2Semantic proximity Read ↗

Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratory.Semantic proximity Read ↗

Multiple approaches for massively parallel sequencing of SARS-CoV-2 genomes directly from clinical samples.Semantic proximity Read ↗

A Comparison of Five Illumina, Ion Torrent, and Nanopore Sequencing Technology-Based Approaches for Whole Genome Sequencing of SARS-CoV-2Semantic proximity Read ↗

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