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Analysis of Wuhan Coronavirus: Deja Vu
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3
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25901
|
February 7, 2020
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Phylodynamic analysis of nCoV-2019 genomes – 29-Jan-2020
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3
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25808
|
January 31, 2020
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Temporal signal and the evolutionary rate of 2019 n-CoV using 47 genomes collected by Feb 01 2020
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4
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12773
|
February 5, 2020
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Long-term evolution of SARS-CoV-2 in an immunocompromised patient with non-Hodgkin lymphoma
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0
|
8902
|
February 18, 2021
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Two Ebola virus variants circulating during the 2020 Equateur Province outbreak
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0
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8820
|
August 15, 2020
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|
A preliminary selection analysis of the South African V501.V2 SARS-CoV-2 clade
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0
|
8646
|
December 29, 2020
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|
Selection analysis identifies significant mutational changes in Omicron that are likely to influence both antibody neutralization and Spike function (Part 2 of 2)
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0
|
8300
|
December 5, 2021
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|
Resurgence of SARS-CoV-2 19B clade corresponds with possible convergent evolution
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2
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4715
|
February 18, 2021
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Emergence of a novel reassortant Oropouche virus drives persistent outbreaks in the Brazilian Amazon region from 2022 to 2024
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1
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18047
|
July 24, 2024
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Phylodynamic analysis of a densely sampled COVID19 outbreak in Weifang, China
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0
|
7730
|
March 10, 2020
|
|
Phylogeography with whole genomes 24 Mar 2020
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0
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7606
|
March 24, 2020
|
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Electron microscopy and a sequence-independent, single-primer amplification (SISPA) viromics approach for monkeypox virus genome determination
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0
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7364
|
September 14, 2022
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B.1.258∆, a SARS-CoV-2 variant with ∆H69/∆V70 in the Spike protein circulating in the Czech Republic and Slovakia
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1
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28844
|
February 11, 2021
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|
Whole-Genome Sequence of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) obtained from a South African Coronavirus Disease 2019 (COVID-19) Patient
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0
|
40601
|
April 1, 2020
|
|
A Monkeypox virus genome from a second Belgian case
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0
|
7209
|
May 23, 2022
|
|
Circulation of 21A (Delta) SARS-CoV-2 variant in Rio Grande do Sul, Southern Brazil
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3
|
6389
|
October 5, 2021
|
|
Spike protein mutations in novel SARS-CoV-2 ‘variants of concern’ commonly occur in or near indels
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2
|
22662
|
April 17, 2022
|
|
Seasonal CoV & SARS CoV Live Full-Genome Builds
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2
|
7118
|
January 28, 2020
|
|
SARS comparison
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1
|
4669
|
February 3, 2020
|
|
Mpox Clade Ib cases in Goma
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0
|
6570
|
March 5, 2024
|
|
Transmission of SARS-CoV-2 Lineage B.1.1.7 in England: Insights from linking epidemiological and genetic data
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1
|
25860
|
December 30, 2020
|
|
Detection of the B.1.1.7 and B.1.351 SARS-CoV-2 variants in Bangladesh
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0
|
6423
|
March 26, 2021
|
|
Serratus: The ultra-deep search to discover novel coronaviruses
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7
|
12167
|
October 11, 2021
|
|
Genomic Surveillance of SARS-CoV-2 in the State of Rio de Janeiro, Brazil: technical briefing
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7
|
12127
|
September 3, 2021
|
|
Two draft Canadian monkeypox virus (MPXV) genomes, June 2022
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0
|
5943
|
June 21, 2022
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|
Omicron is a Multiply Recombinant Set of Variants That Have Evolved Over Many Months
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1
|
23428
|
January 29, 2022
|
|
Phylogenetic analysis of SARS-CoV-2 in DRC
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0
|
5837
|
July 17, 2020
|
|
Spike protein sequences of Cambodian, Thai and Japanese bat sarbecoviruses provide insights into the natural evolution of the Receptor Binding Domain and S1/S2 cleavage site
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1
|
23083
|
May 25, 2021
|
|
Evolutionary & epidemiological analysis of 93 genomes
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|
1
|
12230
|
February 27, 2020
|
|
SARS-CoV-2 diversity in Uganda, December, 2020
|
|
2
|
9914
|
January 6, 2021
|
|
Zika virus protein structure homology modelling
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|
8
|
9979
|
February 10, 2016
|
|
The ongoing evolution of variants of concern and interest of SARS-CoV-2 in Brazil revealed by convergent indels in the amino (N)-terminal domain of the Spike protein
|
|
3
|
14560
|
April 28, 2021
|
|
Tracking the international spread of SARS-CoV-2 lineages B.1.1.7 and B.1.351/501Y-V2
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0
|
29106
|
January 13, 2021
|
|
Assessing evolutionary pressures on the SARS-CoV-2 Mu (B.1.621) clade
|
|
0
|
4786
|
October 8, 2021
|
|
2019 Lassa virus sequencing in Nigeria - 23 additional sequences
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0
|
4683
|
March 12, 2019
|
|
Evidence Against the Veracity of SARS-CoV-2 Genomes Intermediate between Lineages A and B
|
|
0
|
25971
|
September 3, 2021
|
|
Note about availability of H5N1 2.3.4.4b consensus sequences from cattle and other species:
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1
|
10213
|
May 5, 2024
|
|
2018 LASV sequencing, continued
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|
6
|
9613
|
April 17, 2018
|
|
Testing recombination in the pandemic SARS-CoV-2 strains
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0
|
4518
|
May 28, 2020
|
|
Integration of JBrowse 2 genome browser with Nextstrain
|
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0
|
4324
|
March 16, 2021
|
|
Unbiased metagenomic sequencing reveals Hepatitis A virus as an underestimated cause of undiagnosed febrile illness in Kenya
|
|
0
|
4294
|
April 11, 2024
|
|
Vibrio Cholerae Genomics
|
|
0
|
4275
|
June 30, 2023
|
|
Wastewater samples CANNOT be used for genome assembly
|
|
7
|
8379
|
March 3, 2023
|
|
Phylogenetic evidence that B.1.1.7 has been circulating in the United States since early- to mid-November
|
|
0
|
23101
|
January 19, 2021
|
|
Early analysis of 1,093 SARS-CoV2 intra-host variation datasets and comparison with sites under selection
|
|
2
|
7397
|
June 8, 2020
|
|
Guinea 2021 EBOV outbreak
|
|
0
|
22697
|
March 12, 2021
|
|
Assemblies of putative SARS-CoV2-spike-encoding mRNA sequences for vaccines BNT-162b2 and mRNA-1273
|
|
0
|
22110
|
March 24, 2021
|
|
Phylodynamic estimation of incidence and prevalence of novel coronavirus (nCoV) infections through time
|
|
2
|
12659
|
February 14, 2020
|
|
First French draft genome sequence of Monkeypox virus, may 2022
|
|
5
|
8876
|
June 9, 2022
|
|
Report on Omicron Spike mutations on epitopes and immunological/epidemiological/kinetics effects from literature
|
|
0
|
21513
|
November 30, 2021
|