|
Recombinant SARS-CoV-2 genomes involving lineage B.1.1.7 in the UK
|
|
0
|
27642
|
March 17, 2021
|
|
Pango Lineage Nomenclature: provisional rules for naming recombinant lineages
|
|
0
|
19380
|
March 17, 2021
|
|
Integration of JBrowse 2 genome browser with Nextstrain
|
|
0
|
3835
|
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
|
25543
|
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
|
14147
|
March 11, 2021
|
|
Guinea 2021 EBOV genomes
|
|
0
|
14845
|
March 12, 2021
|
|
Guinea 2021 EBOV outbreak
|
|
0
|
21599
|
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
|
10366
|
March 6, 2021
|
|
Emergence and spread of SARS-CoV-2 lineage B.1.1.7 in Brazil
|
|
0
|
5210
|
March 4, 2021
|
|
The emergence of the B.1.1.7 lineage in Jordan
|
|
0
|
5201
|
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
|
42582
|
February 27, 2021
|
|
Global framework for SARS-CoV-2 data analysis: Application to intrahost variation | Part 1
|
|
0
|
4305
|
February 22, 2021
|
|
Long-term evolution of SARS-CoV-2 in an immunocompromised patient with non-Hodgkin lymphoma
|
|
0
|
8407
|
February 18, 2021
|
|
Resurgence of SARS-CoV-2 19B clade corresponds with possible convergent evolution
|
|
2
|
4332
|
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
|
27976
|
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
|
4835
|
February 5, 2021
|
|
Tracking the international spread of SARS-CoV-2 lineages B.1.1.7 and B.1.351/501Y-V2
|
|
0
|
27935
|
January 13, 2021
|
|
Genomic coordinates for B.1.1.7, P.1, and B.1.351
|
|
2
|
5228
|
January 27, 2021
|
|
Gained stops in data from The Peter Doherty Institute for Infection and Immunity
|
|
11
|
6805
|
January 26, 2021
|
|
Multiplexed RT-qPCR to screen for SARS-COV-2 B.1.1.7 variants: Preliminary results
|
|
1
|
11499
|
January 25, 2021
|
|
Genomic characterisation of an emergent SARS-CoV-2 lineage in Manaus: preliminary findings
|
|
1
|
180149
|
January 25, 2021
|
|
Exploring the natural origins of SARS-CoV-2
|
|
0
|
12279
|
January 16, 2021
|
|
Spatio-temporal heterogeneity and the spread of lineage B.1.1.7 in the United Kingdom
|
|
1
|
7367
|
January 20, 2021
|
|
Phylogenetic evidence that B.1.1.7 has been circulating in the United States since early- to mid-November
|
|
0
|
22382
|
January 19, 2021
|
|
Detection of non-B.1.1.7 Spike ∆69/70 sequences (B.1.375) in the United States
|
|
1
|
10750
|
January 14, 2021
|
|
Spike E484K mutation in the first SARS-CoV-2 reinfection case confirmed in Brazil, 2020
|
|
0
|
73224
|
January 10, 2021
|
|
Spike E484K mutation in the first SARS-CoV-2 reinfection case confirmed in Brazil
|
|
0
|
2412
|
January 10, 2021
|
|
SARS-CoV-2 diversity in Uganda, December, 2020
|
|
2
|
9505
|
January 6, 2021
|
|
Updated Nextstain SARS-CoV-2 clade naming strategy
|
|
0
|
60726
|
January 5, 2021
|
|
Identification of a novel SARS-CoV-2 Spike 69-70 deletion lineage circulating in the United States
|
|
1
|
13835
|
December 31, 2020
|