|
About the nCoV-2019 Evolutionary History category
|
|
0
|
1167
|
January 31, 2020
|
|
Tackling Rumors of a Suspicious Origin of nCoV2019
|
|
22
|
48824
|
October 22, 2020
|
|
On the veracity of RaTG13
|
|
8
|
4701
|
September 19, 2020
|
|
Time dependence of SARS-CoV-2 substitution rates
|
|
3
|
2033
|
August 31, 2020
|
|
The Sarbecovirus origin of SARS-CoV-2’s furin cleavage site
|
|
4
|
5766
|
August 9, 2020
|
|
Missed ORFs in nCoV?
|
|
1
|
4285
|
June 9, 2020
|
|
Selection analysis of GISAID SARS-CoV-2 data
|
|
3
|
6167
|
May 5, 2020
|
|
The Proximal Origin of SARS-CoV-2
|
|
4
|
197679
|
March 18, 2020
|
|
Alignment of 58 Sarbecovirus genomes for conservation analysis of SARS-CoV-2
|
|
1
|
4060
|
March 12, 2020
|
|
SARS-CoV-2 Samples from Same Early COVID-19 Patients Were Sequenced Repeatedly with Errors Distorting Phylogenetic Trees
|
|
0
|
4471
|
March 10, 2020
|
|
nCoV-2019 Spike Protein Receptor Binding Domain Shares High Amino Acid Identity With a Coronavirus Recovered from a Pangolin Viral Metagenomic Dataset
|
|
22
|
44498
|
February 27, 2020
|
|
nCoV's relationship to bat coronaviruses & recombination signals (no snakes) - no evidence the 2019-nCoV lineage is recombinant
|
|
23
|
67107
|
February 25, 2020
|
|
Response to nCoV2019 Against Backdrop of Endogenous Retroviruses
|
|
1
|
6109
|
February 14, 2020
|
|
Divergence of nCoV-2019 to closest non-human relative
|
|
2
|
8794
|
February 12, 2020
|
|
Analysis of Wuhan Coronavirus: Deja Vu
|
|
3
|
13074
|
February 7, 2020
|
|
Seasonal CoV & SARS CoV Live Full-Genome Builds
|
|
2
|
3207
|
January 28, 2020
|
|
nCoV-2019 codon usage and reservoir (not snakes v2)
|
|
3
|
19051
|
January 27, 2020
|
