2020
DOI: 10.1101/2020.09.15.20195420
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SARS-CoV-2 genomes from Oklahoma, USA

Abstract: Genomic sequencing has played a major role in understanding the pathogenicity of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). With the current pandemic, it is essential that SARS-CoV-2 viruses are sequenced regularly to determine mutations and genomic modifications in different geographical locations. In this study we sequenced SARS-CoV-2 from 5 clinical samples obtained in Oklahoma, USA during different time points of pandemic presence in the state. One sample from the initial days of the pan… Show more

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Cited by 3 publications
(4 citation statements)
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“…Q27Stop mutation in ORF 8 was detected in 3 out of these 4 samples. N501Y and the previously described D614G mutations (14,15) were detected in all 6 samples (Table 2).…”
Section: Tablesupporting
confidence: 52%
See 1 more Smart Citation
“…Q27Stop mutation in ORF 8 was detected in 3 out of these 4 samples. N501Y and the previously described D614G mutations (14,15) were detected in all 6 samples (Table 2).…”
Section: Tablesupporting
confidence: 52%
“…Annotated genes and the whole genomes were aligned using MUSCLE aligner in MEGA-X (12). The genome sequences were submitted to GISAID (1) and their GISAID classification and PANGO lineages (13) (14,15) were detected in all 6 samples (Table 2).…”
Section: Introductionmentioning
confidence: 99%
“…Due to Covid-19's pandemic magnitude, an immense effort to sequence SARS-CoV-2 genetic variants and its relations to clinical and epidemiological findings has been made worldwide. There are nearly a thousand preprints available about genetic variants, published in https://www.medrxiv.org 1 , https://www.biorxiv.org 2 and some other preprint platforms, which promote the rapid data exchange about SARS-CoV-2 genetic sequences [3][4][5][6][7][8][9][10] , infectivity and lethality (https://nextstrain.org/sars-cov-2/; https://www.ncbi.nlm.nih.gov; https://www.gisaid.org; https://covid.pages.uni.lu; https://www.covid19dataportal.org) [11][12][13][14][15] . Updated mutations on any sequence can be tested in different countries and time periods.…”
Section: Introductionmentioning
confidence: 99%
“…PA acknowledges a grant from NIGMS under award number GM105978. This manuscript has been released as pre-print at medRxiv ( Narayanan et al, 2020 ).…”
mentioning
confidence: 99%