|
Introduction and spread of SARS-CoV-2 in the greater Boston area
|
|
0
|
8876
|
June 4, 2020
|
|
Year-letter Genetic Clade Naming for SARS-CoV-2 on Nextstrain.org
|
|
1
|
15379
|
June 2, 2020
|
|
Introduction and local transmission of SARS-CoV-2 cases in Kenya
|
|
0
|
11810
|
June 2, 2020
|
|
SARS-CoV-2 Genomes from Nigeria Reveal Community Transmission, Multiple Virus Lineages and Spike Protein Mutation Associated with Higher Transmission and Pathogenicity
|
|
0
|
14720
|
May 29, 2020
|
|
Testing recombination in the pandemic SARS-CoV-2 strains
|
|
0
|
3963
|
May 28, 2020
|
|
Common Microdeletions in SARS-CoV-2 Sequences
|
|
0
|
4997
|
May 15, 2020
|
|
Pangolin web application release
|
|
0
|
15892
|
May 13, 2020
|
|
Selection analysis of GISAID SARS-CoV-2 data
|
|
3
|
9491
|
May 5, 2020
|
|
Early phylodynamics analysis of the COVID-19 epidemics in France using 194 genomes - April 10, 2020
|
|
3
|
7869
|
April 29, 2020
|
|
An 81 base-pair deletion in SARS-CoV-2 ORF7a identified from sentinel surveillance in Arizona (Jan-Mar 2020)
|
|
0
|
8200
|
April 22, 2020
|
|
A dynamic nomenclature proposal for SARS-CoV-2 to assist genomic epidemiology
|
|
0
|
13732
|
April 6, 2020
|
|
Phylogeography with whole genomes 24 Mar 2020
|
|
0
|
6971
|
March 24, 2020
|
|
First African SARS-CoV-2 genome sequence from Nigerian COVID-19 case
|
|
1
|
53967
|
March 21, 2020
|
|
Update report of COVID-19 in Scotland: continuing introductions & transmissions
|
|
3
|
7489
|
March 18, 2020
|
|
The Proximal Origin of SARS-CoV-2
|
|
4
|
239716
|
March 18, 2020
|
|
Response to “On the origin and continuing evolution of SARS-CoV-2”
|
|
11
|
121226
|
March 16, 2020
|
|
Phylodynamic Analyses of outbreaks in China, Italy, Washington State (USA), and the Diamond Princess
|
|
1
|
14018
|
March 13, 2020
|
|
Alignment of 58 Sarbecovirus genomes for conservation analysis of SARS-CoV-2
|
|
1
|
8540
|
March 12, 2020
|
|
Phylodynamic analysis of a densely sampled COVID19 outbreak in Weifang, China
|
|
0
|
7053
|
March 10, 2020
|
|
Update report of COVID-19 in Scotland: multiple introductions
|
|
0
|
7568
|
March 10, 2020
|
|
SARS-CoV-2 Samples from Same Early COVID-19 Patients Were Sequenced Repeatedly with Errors Distorting Phylogenetic Trees
|
|
0
|
7365
|
March 10, 2020
|
|
[Update 2] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
8579
|
March 6, 2020
|
|
Phylodynamic analysis of SARS-CoV-2 | Update 2020-03-06
|
|
0
|
12864
|
March 6, 2020
|
|
Phylodynamic Analyses based on 11 genomes from the Italian outbreak
|
|
0
|
6161
|
March 6, 2020
|
|
[Update] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
4200
|
March 4, 2020
|
|
First cases of coronavirus disease (COVID-19) in Brazil, South America (2 genomes, 3rd March 2020)
|
|
1
|
92902
|
February 29, 2020
|
|
Transparent analysis of raw COVID-19 data: lack and low quality of raw data
|
|
2
|
7483
|
February 27, 2020
|
|
nCoV-2019 Spike Protein Receptor Binding Domain Shares High Amino Acid Identity With a Coronavirus Recovered from a Pangolin Viral Metagenomic Dataset
|
|
22
|
58063
|
February 27, 2020
|
|
Evolutionary & epidemiological analysis of 93 genomes
|
|
1
|
11635
|
February 27, 2020
|
|
nCoV's relationship to bat coronaviruses & recombination signals (no snakes) - no evidence the 2019-nCoV lineage is recombinant
|
|
23
|
86793
|
February 25, 2020
|