|
Introduction and local transmission of SARS-CoV-2 cases in Kenya
|
|
0
|
11642
|
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
|
14563
|
May 29, 2020
|
|
Testing recombination in the pandemic SARS-CoV-2 strains
|
|
0
|
3841
|
May 28, 2020
|
|
Common Microdeletions in SARS-CoV-2 Sequences
|
|
0
|
4888
|
May 15, 2020
|
|
Pangolin web application release
|
|
0
|
15521
|
May 13, 2020
|
|
Selection analysis of GISAID SARS-CoV-2 data
|
|
3
|
9357
|
May 5, 2020
|
|
Early phylodynamics analysis of the COVID-19 epidemics in France using 194 genomes - April 10, 2020
|
|
3
|
7683
|
April 29, 2020
|
|
An 81 base-pair deletion in SARS-CoV-2 ORF7a identified from sentinel surveillance in Arizona (Jan-Mar 2020)
|
|
0
|
8081
|
April 22, 2020
|
|
A dynamic nomenclature proposal for SARS-CoV-2 to assist genomic epidemiology
|
|
0
|
13571
|
April 6, 2020
|
|
Phylogeography with whole genomes 24 Mar 2020
|
|
0
|
6820
|
March 24, 2020
|
|
First African SARS-CoV-2 genome sequence from Nigerian COVID-19 case
|
|
1
|
53566
|
March 21, 2020
|
|
Update report of COVID-19 in Scotland: continuing introductions & transmissions
|
|
3
|
7341
|
March 18, 2020
|
|
The Proximal Origin of SARS-CoV-2
|
|
4
|
237892
|
March 18, 2020
|
|
Response to “On the origin and continuing evolution of SARS-CoV-2”
|
|
11
|
120567
|
March 16, 2020
|
|
Phylodynamic Analyses of outbreaks in China, Italy, Washington State (USA), and the Diamond Princess
|
|
1
|
13856
|
March 13, 2020
|
|
Alignment of 58 Sarbecovirus genomes for conservation analysis of SARS-CoV-2
|
|
1
|
8430
|
March 12, 2020
|
|
Phylodynamic analysis of a densely sampled COVID19 outbreak in Weifang, China
|
|
0
|
6916
|
March 10, 2020
|
|
Update report of COVID-19 in Scotland: multiple introductions
|
|
0
|
7394
|
March 10, 2020
|
|
SARS-CoV-2 Samples from Same Early COVID-19 Patients Were Sequenced Repeatedly with Errors Distorting Phylogenetic Trees
|
|
0
|
7281
|
March 10, 2020
|
|
[Update 2] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
8317
|
March 6, 2020
|
|
Phylodynamic analysis of SARS-CoV-2 | Update 2020-03-06
|
|
0
|
12688
|
March 6, 2020
|
|
Phylodynamic Analyses based on 11 genomes from the Italian outbreak
|
|
0
|
6054
|
March 6, 2020
|
|
[Update] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
4137
|
March 4, 2020
|
|
First cases of coronavirus disease (COVID-19) in Brazil, South America (2 genomes, 3rd March 2020)
|
|
1
|
92418
|
February 29, 2020
|
|
Transparent analysis of raw COVID-19 data: lack and low quality of raw data
|
|
2
|
7421
|
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
|
57601
|
February 27, 2020
|
|
Evolutionary & epidemiological analysis of 93 genomes
|
|
1
|
11552
|
February 27, 2020
|
|
nCoV's relationship to bat coronaviruses & recombination signals (no snakes) - no evidence the 2019-nCoV lineage is recombinant
|
|
23
|
85983
|
February 25, 2020
|
|
How close are we to the 'phylodynamic threshold'? A simulation study
|
|
0
|
7788
|
January 31, 2020
|
|
Response to nCoV2019 Against Backdrop of Endogenous Retroviruses
|
|
1
|
49559
|
February 14, 2020
|