|
Global framework for SARS-CoV-2 data analysis: Application to intrahost variation | Part 2
|
|
1
|
2121
|
April 2, 2021
|
|
Detection of a large cluster and multiple introductions of the P.1 SARS-CoV-2 Variant of Concern in Massachusetts
|
|
0
|
5552
|
April 2, 2021
|
|
Genomic characterisation of sylvatic yellow fever virus epizootic in Trinidad
|
|
0
|
1237
|
March 29, 2021
|
|
Detection of the B.1.1.7 and B.1.351 SARS-CoV-2 variants in Bangladesh
|
|
0
|
1962
|
March 26, 2021
|
|
Assemblies of putative SARS-CoV2-spike-encoding mRNA sequences for vaccines BNT-162b2 and mRNA-1273
|
|
0
|
3514
|
March 24, 2021
|
|
Recombinant SARS-CoV-2 genomes involving lineage B.1.1.7 in the UK
|
|
0
|
16164
|
March 17, 2021
|
|
Pango Lineage Nomenclature: provisional rules for naming recombinant lineages
|
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0
|
3039
|
March 17, 2021
|
|
Integration of JBrowse 2 genome browser with Nextstrain
|
|
0
|
952
|
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
|
17693
|
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
|
9332
|
March 11, 2021
|
|
Guinea 2021 EBOV outbreak
|
|
0
|
14392
|
March 12, 2021
|
|
Guinea 2021 EBOV genomes
|
|
0
|
8461
|
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
|
6299
|
March 6, 2021
|
|
Emergence and spread of SARS-CoV-2 lineage B.1.1.7 in Brazil
|
|
0
|
2167
|
March 4, 2021
|
|
The emergence of the B.1.1.7 lineage in Jordan
|
|
0
|
2708
|
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
|
28000
|
February 27, 2021
|
|
Global framework for SARS-CoV-2 data analysis: Application to intrahost variation | Part 1
|
|
0
|
1526
|
February 22, 2021
|
|
Long-term evolution of SARS-CoV-2 in an immunocompromised patient with non-Hodgkin lymphoma
|
|
0
|
3769
|
February 18, 2021
|
|
Resurgence of SARS-CoV-2 19B clade corresponds with possible convergent evolution
|
|
2
|
1857
|
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
|
19785
|
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
|
1918
|
February 5, 2021
|
|
Tracking the international spread of SARS-CoV-2 lineages B.1.1.7 and B.1.351/501Y-V2
|
|
0
|
16859
|
January 13, 2021
|
|
Genomic coordinates for B.1.1.7, P.1, and B.1.351
|
|
2
|
3109
|
January 27, 2021
|
|
Gained stops in data from The Peter Doherty Institute for Infection and Immunity
|
|
11
|
3726
|
January 26, 2021
|
|
Multiplexed RT-qPCR to screen for SARS-COV-2 B.1.1.7 variants: Preliminary results
|
|
1
|
6933
|
January 25, 2021
|
|
Genomic characterisation of an emergent SARS-CoV-2 lineage in Manaus: preliminary findings
|
|
1
|
118515
|
January 25, 2021
|
|
Exploring the natural origins of SARS-CoV-2
|
|
0
|
7341
|
January 16, 2021
|
|
Spike protein mutations in novel SARS-CoV-2 ‘variants of concern’ commonly occur in or near indels
|
|
0
|
9555
|
January 21, 2021
|
|
Spatio-temporal heterogeneity and the spread of lineage B.1.1.7 in the United Kingdom
|
|
1
|
2991
|
January 20, 2021
|
|
Phylogenetic evidence that B.1.1.7 has been circulating in the United States since early- to mid-November
|
|
0
|
16851
|
January 19, 2021
|
