|
Preliminary in silico assessment of the specificity of published molecular assays and design of new assays using the available whole genome sequences of 2019-nCoV
|
|
52
|
29443
|
June 21, 2021
|
|
The Sarbecovirus origin of SARS-CoV-2’s furin cleavage site
|
|
5
|
29204
|
November 23, 2021
|
|
B.1.258∆, a SARS-CoV-2 variant with ∆H69/∆V70 in the Spike protein circulating in the Czech Republic and Slovakia
|
|
1
|
27143
|
February 11, 2021
|
|
Tracking the international spread of SARS-CoV-2 lineages B.1.1.7 and B.1.351/501Y-V2
|
|
0
|
26706
|
January 13, 2021
|
|
Recombinant SARS-CoV-2 genomes involving lineage B.1.1.7 in the UK
|
|
0
|
26648
|
March 17, 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
|
24694
|
March 16, 2021
|
|
Selection analysis identifies significant mutational changes in Omicron that are likely to influence both antibody neutralization and Spike function (Part 1 of 2)
|
|
1
|
23421
|
January 20, 2022
|
|
Analysis of Wuhan Coronavirus: Deja Vu
|
|
3
|
23349
|
February 7, 2020
|
|
Transmission of SARS-CoV-2 Lineage B.1.1.7 in England: Insights from linking epidemiological and genetic data
|
|
1
|
23000
|
December 30, 2020
|
|
Evidence Against the Veracity of SARS-CoV-2 Genomes Intermediate between Lineages A and B
|
|
0
|
22058
|
September 3, 2021
|
|
Phylogenetic evidence that B.1.1.7 has been circulating in the United States since early- to mid-November
|
|
0
|
21815
|
January 19, 2021
|
|
Omicron is a Multiply Recombinant Set of Variants That Have Evolved Over Many Months
|
|
1
|
21514
|
January 29, 2022
|
|
Phylogenetic analysis of 23 nCoV-2019 genomes, 2020-01-23
|
|
7
|
20508
|
February 3, 2020
|
|
Putative host origins of RNA insertions in SARS-CoV-2 genomes
|
|
3
|
19968
|
December 6, 2021
|
|
Report on Omicron Spike mutations on epitopes and immunological/epidemiological/kinetics effects from literature
|
|
0
|
19644
|
November 30, 2021
|
|
Assemblies of putative SARS-CoV2-spike-encoding mRNA sequences for vaccines BNT-162b2 and mRNA-1273
|
|
0
|
18825
|
March 24, 2021
|
|
Phylodynamic analysis of nCoV-2019 genomes – 29-Jan-2020
|
|
3
|
18575
|
January 31, 2020
|
|
Masking strategies for SARS-CoV-2 alignments
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|
17
|
18375
|
September 28, 2021
|
|
Detection of SARS-CoV-2 P681H Spike Protein Variant in Nigeria
|
|
0
|
17819
|
December 23, 2020
|
|
Pango Lineage Nomenclature: provisional rules for naming recombinant lineages
|
|
0
|
17802
|
March 17, 2021
|
|
Genomic epidemiology of early introductions of SARS-CoV-2 into the Canadian province of Québec
|
|
0
|
16418
|
September 18, 2020
|
|
On the veracity of RaTG13
|
|
8
|
15614
|
September 19, 2020
|
|
Pangolin web application release
|
|
0
|
15393
|
May 13, 2020
|
|
Identification of a common deletion in the spike protein of SARS-CoV-2
|
|
15
|
15129
|
June 24, 2020
|
|
Year-letter Genetic Clade Naming for SARS-CoV-2 on Nextstrain.org
|
|
1
|
15068
|
June 2, 2020
|
|
Naturally occurring indels in multiple coronavirus spikes
|
|
3
|
14553
|
November 23, 2020
|
|
SARS-CoV-2 Genomes from Nigeria Reveal Community Transmission, Multiple Virus Lineages and Spike Protein Mutation Associated with Higher Transmission and Pathogenicity
|
|
0
|
14524
|
May 29, 2020
|
|
Initial assessment of the ability of published coronavirus primers sets to detect the Wuhan coronavirus
|
|
0
|
14250
|
January 15, 2020
|
|
Divergence of nCoV-2019 to closest non-human relative
|
|
2
|
14006
|
February 12, 2020
|
|
Phylodynamic Analyses of outbreaks in China, Italy, Washington State (USA), and the Diamond Princess
|
|
1
|
13791
|
March 13, 2020
|