2022
DOI: 10.1101/2022.06.20.22276625
|View full text |Cite
Preprint
|
Sign up to set email alerts
|

Analysis of Whole-Genome Sequencing of SARS-CoV-2 Reveals Recurrent Mutations among Iranian Patients

Abstract: BackgroundSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new emerging coronavirus that causes coronavirus disease 2019 (COVID-19). Whole-genome tracking of the SARS-CoV-2 enhanced our understanding of the mechanism of disease, control, and prevent COVID-19 infections.Materials and MethodsIn the current study, we investigated 1221 SARS-CoV-2 protein sequences of Iranian SARS-CoV-2 in the public database of the GISAID from January 2019 to April 2022. Prepare a list of suitable samples and prep… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
1
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 159 publications
0
1
0
Order By: Relevance
“…Abbasian et al reported the frequency of 21.1% for N-D3L in 1221 SARS-CoV-2 genome sequences of Iran which retrieved from GISAID. They concluded that the occurrence of N-D3L/E/Q has increased from May to December 2020 and wasstablished for several months 23. The emergence of D3Q and D3E in immunocompromised patients after treatment might help to infectivity enhancement in the immunosuppressed situation.Our results in agreement with the previous studies showed some disparate mutations in nonstructural nsp3 protein.…”
mentioning
confidence: 99%
“…Abbasian et al reported the frequency of 21.1% for N-D3L in 1221 SARS-CoV-2 genome sequences of Iran which retrieved from GISAID. They concluded that the occurrence of N-D3L/E/Q has increased from May to December 2020 and wasstablished for several months 23. The emergence of D3Q and D3E in immunocompromised patients after treatment might help to infectivity enhancement in the immunosuppressed situation.Our results in agreement with the previous studies showed some disparate mutations in nonstructural nsp3 protein.…”
mentioning
confidence: 99%