|
Response to “On the origin and continuing evolution of SARS-CoV-2”
|
|
11
|
125177
|
March 16, 2020
|
|
Phylodynamic Analyses of outbreaks in China, Italy, Washington State (USA), and the Diamond Princess
|
|
1
|
14699
|
March 13, 2020
|
|
Alignment of 58 Sarbecovirus genomes for conservation analysis of SARS-CoV-2
|
|
1
|
9092
|
March 12, 2020
|
|
Phylodynamic analysis of a densely sampled COVID19 outbreak in Weifang, China
|
|
0
|
7604
|
March 10, 2020
|
|
Update report of COVID-19 in Scotland: multiple introductions
|
|
0
|
8090
|
March 10, 2020
|
|
SARS-CoV-2 Samples from Same Early COVID-19 Patients Were Sequenced Repeatedly with Errors Distorting Phylogenetic Trees
|
|
0
|
7825
|
March 10, 2020
|
|
[Update 2] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
9350
|
March 6, 2020
|
|
Phylodynamic analysis of SARS-CoV-2 | Update 2020-03-06
|
|
0
|
13810
|
March 6, 2020
|
|
Phylodynamic Analyses based on 11 genomes from the Italian outbreak
|
|
0
|
6643
|
March 6, 2020
|
|
[Update] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
4507
|
March 4, 2020
|
|
First cases of coronavirus disease (COVID-19) in Brazil, South America (2 genomes, 3rd March 2020)
|
|
1
|
95724
|
February 29, 2020
|
|
Transparent analysis of raw COVID-19 data: lack and low quality of raw data
|
|
2
|
7874
|
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
|
60913
|
February 27, 2020
|
|
Evolutionary & epidemiological analysis of 93 genomes
|
|
1
|
12075
|
February 27, 2020
|
|
nCoV's relationship to bat coronaviruses & recombination signals (no snakes) - no evidence the 2019-nCoV lineage is recombinant
|
|
23
|
91823
|
February 25, 2020
|
|
How close are we to the 'phylodynamic threshold'? A simulation study
|
|
0
|
8917
|
January 31, 2020
|
|
Response to nCoV2019 Against Backdrop of Endogenous Retroviruses
|
|
1
|
53247
|
February 14, 2020
|
|
Phylodynamic estimation of incidence and prevalence of novel coronavirus (nCoV) infections through time
|
|
2
|
12381
|
February 14, 2020
|
|
Wuhan Convalescent Serum and Cells
|
|
0
|
3511
|
February 8, 2020
|
|
Divergence of nCoV-2019 to closest non-human relative
|
|
2
|
15502
|
February 12, 2020
|
|
Number of mutations along a transmission chain
|
|
0
|
5053
|
January 31, 2020
|
|
Sequencing technology and sequence variation in nCoV-2019
|
|
0
|
5620
|
February 2, 2020
|
|
Analysis of Wuhan Coronavirus: Deja Vu
|
|
3
|
25478
|
February 7, 2020
|
|
Novel 2019 coronavirus genome
|
|
27
|
419003
|
February 5, 2020
|
|
Temporal signal and the evolutionary rate of 2019 n-CoV using 47 genomes collected by Feb 01 2020
|
|
4
|
12508
|
February 5, 2020
|
|
SARS comparison
|
|
1
|
4591
|
February 3, 2020
|
|
Genome sequences by date and location
|
|
2
|
5291
|
February 3, 2020
|
|
Initial assessment of the ability of published coronavirus primers sets to detect the Wuhan coronavirus
|
|
0
|
15225
|
January 15, 2020
|
|
Phylodynamic analysis of nCoV-2019 genomes – 29-Jan-2020
|
|
3
|
24669
|
January 31, 2020
|
|
Seasonal CoV & SARS CoV Live Full-Genome Builds
|
|
2
|
6972
|
January 28, 2020
|