|
About the SARS-CoV-2 coronavirus category
|
|
0
|
8411
|
January 9, 2020
|
|
SARS-CoV-2 Spike displays multiple adaptive changes in addition to the furin cleavage site
|
|
3
|
2595
|
July 18, 2025
|
|
SARS-CoV-2 evolution, post-Omicron
|
|
1
|
44192
|
August 30, 2023
|
|
Detection of a SARS-CoV-2 Beta-like Variant with Additional Mutations in Coastal Kenya after >1 Year of Disappearance
|
|
0
|
10899
|
November 7, 2022
|
|
Towards Pandemic-Scale Ancestral Recombination Graphs of SARS-CoV-2
|
|
0
|
4260
|
June 9, 2023
|
|
Repeated loss of ORF8 expression in circulating SARS-CoV-2 lineages
|
|
0
|
9778
|
April 26, 2023
|
|
Wastewater samples CANNOT be used for genome assembly
|
|
7
|
8410
|
March 3, 2023
|
|
The comparative recency of the proximal ancestors of SARS-CoV-1 and SARS-CoV-2
|
|
1
|
14140
|
December 22, 2022
|
|
Issue with pipelines using bcftools to calling consensus in low-coverage regions
|
|
1
|
7488
|
October 19, 2022
|
|
Linking Genotype to Phenotype: Further Exploration of Mutations in SARS-CoV-2 Associated with Mild or Severe Outcomes
|
|
0
|
6946
|
April 15, 2022
|
|
Rapid Establishment of Omicron Variant in Rio Grande do Sul State, Brazil
|
|
3
|
7493
|
May 30, 2022
|
|
Using VariantHunter for detecting emerging SARS-CoV-2 variants
|
|
0
|
3011
|
May 11, 2022
|
|
Spike protein mutations in novel SARS-CoV-2 ‘variants of concern’ commonly occur in or near indels
|
|
2
|
22703
|
April 17, 2022
|
|
Evolutionary rate of SARS-CoV-2 increases during zoonotic infection of farmed mink
|
|
0
|
3880
|
April 7, 2022
|
|
Issues with SARS-CoV-2 sequencing data
|
|
15
|
73115
|
April 5, 2022
|
|
Tackling Rumors of a Suspicious Origin of nCoV2019
|
|
29
|
104198
|
April 1, 2022
|
|
Erroneous Mutations Associated with 64_L-60_R Primer-Dimer in ARTIC 4/4.1
|
|
0
|
3200
|
March 31, 2022
|
|
Mutations arising in SARS-CoV-2 spike on sustained human-to-human transmission and human-to-animal passage
|
|
12
|
65706
|
February 22, 2022
|
|
The dissemination of the Omicron variant in the highly seroprevalent Amazonas state, Brazil, is associated with a rapid upsurge of SARS-CoV-2 cases
|
|
0
|
7798
|
February 5, 2022
|
|
Continued genomic Surveillance of SARS-CoV-2 in the state of Rio de Janeiro, Brazil, by the Corona-ômica-RJ Network
|
|
0
|
3640
|
January 31, 2022
|
|
Omicron is a Multiply Recombinant Set of Variants That Have Evolved Over Many Months
|
|
1
|
23447
|
January 29, 2022
|
|
SARS-CoV-2 lineage assignment is more stable with UShER
|
|
0
|
9674
|
January 20, 2022
|
|
Selection analysis identifies significant mutational changes in Omicron that are likely to influence both antibody neutralization and Spike function (Part 1 of 2)
|
|
1
|
26150
|
January 20, 2022
|
|
Evidence for coordinated evolution at SARS-CoV-2 spike sites that carry Omicron characteristic mutations
|
|
0
|
5143
|
December 30, 2021
|
|
Computational analysis of the effect of SARS-CoV-2 variant Omicron Spike protein mutations on dynamics, ACE2 binding and propensity for immune escape
|
|
1
|
7899
|
December 22, 2021
|
|
A fool’s errand: predicting the evolutionary future of the Omicron SARS-CoV-2 lineage
|
|
0
|
7203
|
December 10, 2021
|
|
Putative host origins of RNA insertions in SARS-CoV-2 genomes
|
|
3
|
22102
|
December 6, 2021
|
|
Selection analysis identifies significant mutational changes in Omicron that are likely to influence both antibody neutralization and Spike function (Part 2 of 2)
|
|
0
|
8307
|
December 5, 2021
|
|
Report on Omicron Spike mutations on epitopes and immunological/epidemiological/kinetics effects from literature
|
|
0
|
21527
|
November 30, 2021
|
|
Mutagenic antivirals: the evolutionary risk of low doses
|
|
0
|
12254
|
November 29, 2021
|