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COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest Chen, Albert Tian; Altschuler, Kevin; Zhan, Shing Hei; Chan, Yujia Alina; Deverman, Benjamin E.
Abstract
COVID-19 CG (covidcg.org) is an open resource for tracking SARS-CoV-2 singlenucleotide variations (SNVs), lineages, and clades using the virus genomes on the GISAID database while filtering by location, date, gene, and mutation of interest. COVID-19 CG provides significant time, labor, and cost-saving utility to projects on SARS-CoV-2 transmission, evolution, diagnostics, therapeutics, vaccines, and intervention tracking. Here, we describe case studies in which users can interrogate (1) SNVs in the SARS-CoV-2 spike receptor binding domain (RBD) across different geographical regions to inform the design and testing of therapeutics, (2) SNVs that may impact the sensitivity of commonly used diagnostic primers, and (3) the emergence of a dominant lineage harboring an S477N RBD mutation in Australia in 2020. To accelerate COVID-19 efforts, COVID-19 CG will be upgraded with new features for users to rapidly pinpoint mutations as the virus evolves throughout the pandemic and in response to therapeutic and public health interventions.
Item Metadata
Title |
COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest
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Creator | |
Contributor | |
Publisher |
eLife
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Date Issued |
2021-02-23
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Description |
COVID-19 CG (covidcg.org) is an open resource for tracking SARS-CoV-2 singlenucleotide variations (SNVs), lineages, and clades using the virus genomes on the GISAID database
while filtering by location, date, gene, and mutation of interest. COVID-19 CG provides significant
time, labor, and cost-saving utility to projects on SARS-CoV-2 transmission, evolution, diagnostics,
therapeutics, vaccines, and intervention tracking. Here, we describe case studies in which users can
interrogate (1) SNVs in the SARS-CoV-2 spike receptor binding domain (RBD) across different
geographical regions to inform the design and testing of therapeutics, (2) SNVs that may impact
the sensitivity of commonly used diagnostic primers, and (3) the emergence of a dominant lineage
harboring an S477N RBD mutation in Australia in 2020. To accelerate COVID-19 efforts, COVID-19
CG will be upgraded with new features for users to rapidly pinpoint mutations as the virus evolves
throughout the pandemic and in response to therapeutic and public health interventions.
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Genre | |
Type | |
Language |
eng
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Date Available |
2021-04-13
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Provider |
Vancouver : University of British Columbia Library
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Rights |
Attribution 4.0 International
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DOI |
10.14288/1.0396668
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URI | |
Affiliation | |
Citation |
Chen, A. T., Altschuler, K., Zhan, S. H., Chan, Y. A., & Deverman, B. E. (2021). COVID-19 CG enables SARS-CoV-2 mutation and lineage tracking by locations and dates of interest. Elife, 10.
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Publisher DOI |
10.7554/eLife.63409
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Peer Review Status |
Reviewed
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Scholarly Level |
Faculty; Researcher; Other
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Copyright Holder |
Chen et al.
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Rights URI | |
Aggregated Source Repository |
DSpace
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Item Media
Item Citations and Data
Rights
Attribution 4.0 International