|
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
|
14790
|
March 11, 2021
|
|
Phylogenetic relationship of SARS-CoV-2 sequences from Amazonas with emerging Brazilian variants harboring mutations E484K and N501Y in the Spike protein
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2
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44443
|
February 27, 2021
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B.1.258∆, a SARS-CoV-2 variant with ∆H69/∆V70 in the Spike protein circulating in the Czech Republic and Slovakia
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1
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28861
|
February 11, 2021
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Tracking the international spread of SARS-CoV-2 lineages B.1.1.7 and B.1.351/501Y-V2
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0
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29162
|
January 13, 2021
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Genomic characterisation of an emergent SARS-CoV-2 lineage in Manaus: preliminary findings
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1
|
188967
|
January 25, 2021
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Spatio-temporal heterogeneity and the spread of lineage B.1.1.7 in the United Kingdom
|
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1
|
7787
|
January 20, 2021
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|
Phylogenetic evidence that B.1.1.7 has been circulating in the United States since early- to mid-November
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0
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23170
|
January 19, 2021
|
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Detection of non-B.1.1.7 Spike ∆69/70 sequences (B.1.375) in the United States
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1
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11347
|
January 14, 2021
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Spike E484K mutation in the first SARS-CoV-2 reinfection case confirmed in Brazil, 2020
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0
|
74981
|
January 10, 2021
|
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Spike E484K mutation in the first SARS-CoV-2 reinfection case confirmed in Brazil
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0
|
2620
|
January 10, 2021
|
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Updated Nextstain SARS-CoV-2 clade naming strategy
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0
|
61321
|
January 5, 2021
|
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Transmission of SARS-CoV-2 Lineage B.1.1.7 in England: Insights from linking epidemiological and genetic data
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1
|
25906
|
December 30, 2020
|
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Lineage-specific growth of SARS-CoV-2 B.1.1.7 during the English national lockdown
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1
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39386
|
December 30, 2020
|
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Detection of SARS-CoV-2 P681H Spike Protein Variant in Nigeria
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0
|
19120
|
December 23, 2020
|
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Preliminary genomic characterisation of an emergent SARS-CoV-2 lineage in the UK defined by a novel set of spike mutations
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4
|
423251
|
December 21, 2020
|
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Genomic epidemiology of the early stages of SARS-CoV-2 outbreak in Russia
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6
|
5975
|
December 8, 2020
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Genomic epidemiology of hCoV-19 in Guangdong Province, China
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0
|
12783
|
March 9, 2020
|
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SARS-CoV-2 spatial structure 2: New evidence from RNA and protein sequences
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0
|
4059
|
July 22, 2020
|
|
Genomic epidemiology of early introductions of SARS-CoV-2 into the Canadian province of Québec
|
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0
|
18370
|
September 18, 2020
|
|
SARS-CoV-2 genomic epidemiology in Sierra Leone
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0
|
4842
|
August 26, 2020
|
|
How many imports of virus from Asian and Europe into USA?
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0
|
2829
|
July 19, 2020
|
|
Phylogenetic analysis of SARS-CoV-2 in DRC
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0
|
5852
|
July 17, 2020
|
|
Spike protein D614G variant paper published in Cell today
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2
|
6152
|
July 3, 2020
|
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Preliminary analysis of SARS-CoV-2 importation & establishment of UK transmission lineages
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6
|
62216
|
June 26, 2020
|
|
Genomic surveillance of SARS-CoV-2 reveals community transmission of a major lineage during the early pandemic phase in Brazil
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0
|
9474
|
June 11, 2020
|
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Introduction and spread of SARS-CoV-2 in the greater Boston area
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0
|
9737
|
June 4, 2020
|
|
Testing recombination in the pandemic SARS-CoV-2 strains
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0
|
4532
|
May 28, 2020
|
|
Common Microdeletions in SARS-CoV-2 Sequences
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0
|
5636
|
May 15, 2020
|
|
Early phylodynamics analysis of the COVID-19 epidemics in France using 194 genomes - April 10, 2020
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|
3
|
8729
|
April 29, 2020
|
|
Phylogeography with whole genomes 24 Mar 2020
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0
|
7628
|
March 24, 2020
|