Response to βOn the origin and continuing evolution of SARS-CoV-2β
|
|
11
|
123275
|
March 16, 2020
|
Phylodynamic Analyses of outbreaks in China, Italy, Washington State (USA), and the Diamond Princess
|
|
1
|
14419
|
March 13, 2020
|
Phylodynamic analysis of a densely sampled COVID19 outbreak in Weifang, China
|
|
0
|
7372
|
March 10, 2020
|
[Update 2] Evolutionary & epidemiological analysis of 128 genomes
|
|
0
|
8953
|
March 6, 2020
|
Phylodynamic analysis of SARS-CoV-2 | Update 2020-03-06
|
|
0
|
13326
|
March 6, 2020
|
Phylodynamic Analyses based on 11 genomes from the Italian outbreak
|
|
0
|
6400
|
March 6, 2020
|
[Update] Evolutionary & epidemiological analysis of 128 genomes
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|
0
|
4376
|
March 4, 2020
|
Evolutionary & epidemiological analysis of 93 genomes
|
|
1
|
11832
|
February 27, 2020
|
How close are we to the 'phylodynamic threshold'? A simulation study
|
|
0
|
8485
|
January 31, 2020
|
Phylodynamic estimation of incidence and prevalence of novel coronavirus (nCoV) infections through time
|
|
2
|
11834
|
February 14, 2020
|
Number of mutations along a transmission chain
|
|
0
|
4895
|
January 31, 2020
|
Sequencing technology and sequence variation in nCoV-2019
|
|
0
|
5432
|
February 2, 2020
|
Temporal signal and the evolutionary rate of 2019 n-CoV using 47 genomes collected by Feb 01 2020
|
|
4
|
12019
|
February 5, 2020
|
SARS comparison
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|
1
|
4477
|
February 3, 2020
|
Genome sequences by date and location
|
|
2
|
5158
|
February 3, 2020
|
Phylodynamic analysis of nCoV-2019 genomes β 29-Jan-2020
|
|
3
|
21311
|
January 31, 2020
|
Phylogenetic analysis of 23 nCoV-2019 genomes, 2020-01-23
|
|
7
|
21598
|
February 3, 2020
|
Clock and TMRCA based on 27 genomes
|
|
5
|
73044
|
January 28, 2020
|
Further musings on the tMRCA
|
|
5
|
7092
|
January 27, 2020
|
Epidemiological Data from the nCoV-2019 Outbreak: Early Descriptions from Publicly Available Data
|
|
2
|
34071
|
January 25, 2020
|
Preliminary phylogenetic analysis of 11 nCoV2019 genomes, 2020-01-19
|
|
2
|
57614
|
January 29, 2020
|