|
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
|
13639
|
March 11, 2021
|
|
A dynamic nomenclature proposal for SARS-CoV-2 to assist genomic epidemiology
|
|
0
|
13567
|
April 6, 2020
|
|
Identification of a novel SARS-CoV-2 Spike 69-70 deletion lineage circulating in the United States
|
|
1
|
13362
|
December 31, 2020
|
|
The ongoing evolution of variants of concern and interest of SARS-CoV-2 in Brazil revealed by convergent indels in the amino (N)-terminal domain of the Spike protein
|
|
3
|
13163
|
April 28, 2021
|
|
First report of COVID-19 in Scotland
|
|
1
|
12986
|
June 9, 2020
|
|
Phylodynamic analysis of SARS-CoV-2 | Update 2020-03-06
|
|
0
|
12688
|
March 6, 2020
|
|
The comparative recency of the proximal ancestors of SARS-CoV-1 and SARS-CoV-2
|
|
1
|
12324
|
December 22, 2022
|
|
Genomic epidemiology of hCoV-19 in Guangdong Province, China
|
|
0
|
12062
|
March 9, 2020
|
|
Exploring the natural origins of SARS-CoV-2
|
|
0
|
11784
|
January 16, 2021
|
|
Introduction and local transmission of SARS-CoV-2 cases in Kenya
|
|
0
|
11642
|
June 2, 2020
|
|
Evolutionary & epidemiological analysis of 93 genomes
|
|
1
|
11552
|
February 27, 2020
|
|
Temporal signal and the evolutionary rate of 2019 n-CoV using 47 genomes collected by Feb 01 2020
|
|
4
|
11101
|
February 5, 2020
|
|
Multiplexed RT-qPCR to screen for SARS-COV-2 B.1.1.7 variants: Preliminary results
|
|
1
|
11058
|
January 25, 2021
|
|
Phylodynamic estimation of incidence and prevalence of novel coronavirus (nCoV) infections through time
|
|
2
|
11001
|
February 14, 2020
|
|
New SARS-CoV-2 Genomes from Nigeria Reveals Dominance of Viruses with Spike Protein Mutation (D614G), and Additional Virus Lineages in Circulation
|
|
0
|
10997
|
July 12, 2020
|
|
Mutagenic antivirals: the evolutionary risk of low doses
|
|
0
|
10757
|
November 29, 2021
|
|
Genomic Surveillance of SARS-CoV-2 in the State of Rio de Janeiro, Brazil: technical briefing
|
|
7
|
10722
|
September 3, 2021
|
|
Serratus: The ultra-deep search to discover novel coronaviruses
|
|
7
|
10718
|
October 11, 2021
|
|
Detection of Spike Mutations; D80G, T95I, G142D, △144, N439K, E484K, P681H, I1130V, and D1139H, in B.1.1.482 Lineage (AV.1) Samples from South Yorkshire, UK
|
|
1
|
10420
|
May 23, 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
|
10401
|
April 6, 2021
|
|
Identification of SARS-CoV-2 P.1-related lineages in Brazil provides new insights about the mechanisms of emergence of Variants of Concern
|
|
0
|
10158
|
May 16, 2021
|
|
Detection of non-B.1.1.7 Spike ∆69/70 sequences (B.1.375) in the United States
|
|
1
|
10122
|
January 14, 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
|
9894
|
March 6, 2021
|
|
Detection of a SARS-CoV-2 Beta-like Variant with Additional Mutations in Coastal Kenya after >1 Year of Disappearance
|
|
0
|
9428
|
November 7, 2022
|
|
Selection analysis of GISAID SARS-CoV-2 data
|
|
3
|
9353
|
May 5, 2020
|
|
Missing G21987A mutation in SARS-CoV-2 delta variants due to non-specific amplification by ARTIC v3 primers
|
|
11
|
9287
|
October 20, 2021
|
|
Emergence and spread of SARS-CoV-2 P.1 (Gamma) lineage variants carrying Spike mutations 𝚫141-144, N679K or P681H during persistent viral circulation in Amazonas, Brazil
|
|
0
|
9239
|
July 4, 2021
|
|
SARS-CoV-2 diversity in Uganda, December, 2020
|
|
2
|
9003
|
January 6, 2021
|
|
Introduction and spread of SARS-CoV-2 in the greater Boston area
|
|
0
|
8675
|
June 4, 2020
|
|
Emergence of lineage B.1.621 in Latin America and the Caribbean
|
|
1
|
8604
|
September 1, 2021
|