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Alignment of 58 Sarbecovirus genomes for conservation analysis of SARS-CoV-2
|
|
1
|
8428
|
March 12, 2020
|
|
Genomic surveillance of SARS-CoV-2 reveals community transmission of a major lineage during the early pandemic phase in Brazil
|
|
0
|
8405
|
June 11, 2020
|
|
Detection of a large cluster and multiple introductions of the P.1 SARS-CoV-2 Variant of Concern in Massachusetts
|
|
0
|
8344
|
April 2, 2021
|
|
[Update 2] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
8309
|
March 6, 2020
|
|
An 81 base-pair deletion in SARS-CoV-2 ORF7a identified from sentinel surveillance in Arizona (Jan-Mar 2020)
|
|
0
|
8079
|
April 22, 2020
|
|
Long-term evolution of SARS-CoV-2 in an immunocompromised patient with non-Hodgkin lymphoma
|
|
0
|
8071
|
February 18, 2021
|
|
Spread of endemic SARS-CoV-2 lineages in Russia
|
|
2
|
7959
|
May 24, 2021
|
|
SARS-CoV-2 lineage assignment is more stable with UShER
|
|
0
|
7837
|
January 20, 2022
|
|
A preliminary selection analysis of the South African V501.V2 SARS-CoV-2 clade
|
|
0
|
7824
|
December 29, 2020
|
|
How close are we to the 'phylodynamic threshold'? A simulation study
|
|
0
|
7783
|
January 31, 2020
|
|
Early phylodynamics analysis of the COVID-19 epidemics in France using 194 genomes - April 10, 2020
|
|
3
|
7677
|
April 29, 2020
|
|
Repeated loss of ORF8 expression in circulating SARS-CoV-2 lineages
|
|
0
|
7651
|
April 26, 2023
|
|
Potential novel SARS-CoV-2 variant of interest from lineage AP.1 with N501Y and additional spike mutations identified in Saxony, Germany
|
|
0
|
7609
|
April 6, 2021
|
|
About the SARS-CoV-2 coronavirus category
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|
0
|
7541
|
January 9, 2020
|
|
Transparent analysis of raw COVID-19 data: lack and low quality of raw data
|
|
2
|
7420
|
February 27, 2020
|
|
Update report of COVID-19 in Scotland: multiple introductions
|
|
0
|
7392
|
March 10, 2020
|
|
Selection analysis identifies significant mutational changes in Omicron that are likely to influence both antibody neutralization and Spike function (Part 2 of 2)
|
|
0
|
7391
|
December 5, 2021
|
|
Update report of COVID-19 in Scotland: continuing introductions & transmissions
|
|
3
|
7335
|
March 18, 2020
|
|
SARS-CoV-2 Samples from Same Early COVID-19 Patients Were Sequenced Repeatedly with Errors Distorting Phylogenetic Trees
|
|
0
|
7280
|
March 10, 2020
|
|
The molecular clock of variants of concern
|
|
3
|
7252
|
August 7, 2021
|
|
Increasing frequency of SARS-CoV-2 lineages B.1.1.7, P.1 and P.2 and identification of a novel lineage harboring E484Q and N501T spike mutations in Minas Gerais, Southeast Brazil
|
|
0
|
7058
|
April 8, 2021
|
|
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
|
6970
|
February 5, 2022
|
|
Phylodynamic analysis of a densely sampled COVID19 outbreak in Weifang, China
|
|
0
|
6912
|
March 10, 2020
|
|
Spatio-temporal heterogeneity and the spread of lineage B.1.1.7 in the United Kingdom
|
|
1
|
6908
|
January 20, 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
|
6856
|
December 22, 2021
|
|
Phylogeography with whole genomes 24 Mar 2020
|
|
0
|
6818
|
March 24, 2020
|
|
Phylogenetic and Recombination Analysis of SARS-CoV-2-like Viruses
|
|
1
|
6779
|
April 17, 2021
|
|
Wastewater samples CANNOT be used for genome assembly
|
|
7
|
6731
|
March 3, 2023
|
|
Recent evolution and international transmission of SARS-CoV-2 clade 19B (Pango A lineages)
|
|
0
|
6690
|
June 2, 2021
|
|
Early analysis of 1,093 SARS-CoV2 intra-host variation datasets and comparison with sites under selection
|
|
2
|
6582
|
June 8, 2020
|