Response to βOn the origin and continuing evolution of SARS-CoV-2β
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|
11
|
119849
|
March 16, 2020
|
Phylodynamic Analyses of outbreaks in China, Italy, Washington State (USA), and the Diamond Princess
|
|
1
|
13739
|
March 13, 2020
|
Phylodynamic analysis of a densely sampled COVID19 outbreak in Weifang, China
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|
0
|
6782
|
March 10, 2020
|
[Update 2] Evolutionary & epidemiological analysis of 128 genomes
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|
0
|
8128
|
March 6, 2020
|
Phylodynamic analysis of SARS-CoV-2 | Update 2020-03-06
|
|
0
|
12518
|
March 6, 2020
|
Phylodynamic Analyses based on 11 genomes from the Italian outbreak
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|
0
|
5959
|
March 6, 2020
|
[Update] Evolutionary & epidemiological analysis of 128 genomes
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|
0
|
4103
|
March 4, 2020
|
Evolutionary & epidemiological analysis of 93 genomes
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|
1
|
11492
|
February 27, 2020
|
How close are we to the 'phylodynamic threshold'? A simulation study
|
|
0
|
7595
|
January 31, 2020
|
Phylodynamic estimation of incidence and prevalence of novel coronavirus (nCoV) infections through time
|
|
2
|
10816
|
February 14, 2020
|
Number of mutations along a transmission chain
|
|
0
|
4656
|
January 31, 2020
|
Sequencing technology and sequence variation in nCoV-2019
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|
0
|
5106
|
February 2, 2020
|
Temporal signal and the evolutionary rate of 2019 n-CoV using 47 genomes collected by Feb 01 2020
|
|
4
|
10864
|
February 5, 2020
|
SARS comparison
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|
1
|
4226
|
February 3, 2020
|
Genome sequences by date and location
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|
2
|
4816
|
February 3, 2020
|
Phylodynamic analysis of nCoV-2019 genomes β 29-Jan-2020
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|
3
|
18450
|
January 31, 2020
|
Phylogenetic analysis of 23 nCoV-2019 genomes, 2020-01-23
|
|
7
|
20381
|
February 3, 2020
|
Clock and TMRCA based on 27 genomes
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|
5
|
64170
|
January 28, 2020
|
Further musings on the tMRCA
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|
5
|
6353
|
January 27, 2020
|
Epidemiological Data from the nCoV-2019 Outbreak: Early Descriptions from Publicly Available Data
|
|
2
|
32029
|
January 25, 2020
|
Preliminary phylogenetic analysis of 11 nCoV2019 genomes, 2020-01-19
|
|
2
|
55057
|
January 29, 2020
|