|
Masking strategies for SARS-CoV-2 alignments
|
|
13
|
9095
|
April 13, 2021
|
|
Issues with SARS-CoV-2 sequencing data
|
|
13
|
33501
|
April 13, 2021
|
|
Detection of the recurrent substitution Q677H in the spike protein of SARS-CoV-2 in cases descended from the lineage B.1.429
|
|
0
|
3232
|
March 20, 2021
|
|
CoVizu: Rapid analysis and visualization of the global diversity of SARS-CoV-2 genomes
|
|
0
|
1611
|
April 12, 2021
|
|
Potential novel SARS-CoV-2 variant of interest from lineage AP.1 with N501Y and additional spike mutations identified in Saxony, Germany
|
|
0
|
2487
|
April 6, 2021
|
|
Increasing frequency of SARS-CoV-2 lineages B.1.1.7, P.1 and P.2 and identification of a novel lineage harboring E484Q and N501T spike mutations in Minas Gerais, Southeast Brazil
|
|
0
|
3957
|
April 8, 2021
|
|
Identification of a new B.1.1.33 SARS-CoV-2 Variant of Interest (VOI) circulating in Brazil with mutation E484K and multiple deletions in the amino (N)-terminal domain of the Spike protein
|
|
0
|
5420
|
April 6, 2021
|
|
Ready-to-use global platform for variant detection in SARS-CoV-2
|
|
0
|
1236
|
April 2, 2021
|
|
Global framework for SARS-CoV-2 data analysis: Application to intrahost variation | Part 2
|
|
1
|
2259
|
April 2, 2021
|
|
Detection of a large cluster and multiple introductions of the P.1 SARS-CoV-2 Variant of Concern in Massachusetts
|
|
0
|
5689
|
April 2, 2021
|
|
Genomic characterisation of sylvatic yellow fever virus epizootic in Trinidad
|
|
0
|
1358
|
March 29, 2021
|
|
Detection of the B.1.1.7 and B.1.351 SARS-CoV-2 variants in Bangladesh
|
|
0
|
2167
|
March 26, 2021
|
|
Assemblies of putative SARS-CoV2-spike-encoding mRNA sequences for vaccines BNT-162b2 and mRNA-1273
|
|
0
|
4042
|
March 24, 2021
|
|
Recombinant SARS-CoV-2 genomes involving lineage B.1.1.7 in the UK
|
|
0
|
17550
|
March 17, 2021
|
|
Pango Lineage Nomenclature: provisional rules for naming recombinant lineages
|
|
0
|
4138
|
March 17, 2021
|
|
Integration of JBrowse 2 genome browser with Nextstrain
|
|
0
|
1075
|
March 16, 2021
|
|
Tracking SARS-CoV-2 VOC 202012/01 (lineage B.1.1.7) dissemination in Portugal: insights from nationwide RT-PCR Spike gene drop out data
|
|
10
|
18208
|
March 16, 2021
|
|
A potential SARS-CoV-2 variant of interest (VOI) harboring mutation E484K in the Spike protein was identified within lineage B.1.1.33 circulating in Brazil
|
|
0
|
9753
|
March 11, 2021
|
|
Guinea 2021 EBOV outbreak
|
|
0
|
14778
|
March 12, 2021
|
|
Guinea 2021 EBOV genomes
|
|
0
|
8846
|
March 12, 2021
|
|
The emergence and ongoing convergent evolution of the N501Y lineages coincided with a major global shift in the SARS-Cov-2 selective landscape
|
|
1
|
6490
|
March 6, 2021
|
|
Emergence and spread of SARS-CoV-2 lineage B.1.1.7 in Brazil
|
|
0
|
2363
|
March 4, 2021
|
|
The emergence of the B.1.1.7 lineage in Jordan
|
|
0
|
2819
|
February 27, 2021
|
|
Phylogenetic relationship of SARS-CoV-2 sequences from Amazonas with emerging Brazilian variants harboring mutations E484K and N501Y in the Spike protein
|
|
2
|
28903
|
February 27, 2021
|
|
Global framework for SARS-CoV-2 data analysis: Application to intrahost variation | Part 1
|
|
0
|
1666
|
February 22, 2021
|
|
Long-term evolution of SARS-CoV-2 in an immunocompromised patient with non-Hodgkin lymphoma
|
|
0
|
4005
|
February 18, 2021
|
|
Resurgence of SARS-CoV-2 19B clade corresponds with possible convergent evolution
|
|
2
|
2018
|
February 18, 2021
|
|
B.1.258∆, a SARS-CoV-2 variant with ∆H69/∆V70 in the Spike protein circulating in the Czech Republic and Slovakia
|
|
1
|
20321
|
February 11, 2021
|
|
A novel, room temperature-stable, multiplexed RT-qPCR assay to distinguish lineage B.1.1.7 from the remaining SARS-CoV-2 lineages
|
|
0
|
2021
|
February 5, 2021
|
|
Tracking the international spread of SARS-CoV-2 lineages B.1.1.7 and B.1.351/501Y-V2
|
|
0
|
17586
|
January 13, 2021
|
