Your browser doesn't support javascript.
loading
SARS-CoV-2 testing in the community: Testing positive samples with the TaqMan SARS-CoV-2 Mutation Panel to find variants in real-time
Fiona Ashford; Angus Best; Steven Dunn; Zahra Ahmed; Henna Siddiqui; Jordan Melville; Samuel Wilkinson; Jeremy Mirza; Nicola Cumley; Joanna Stockton; Jack Ferguson; Lucy Wheatley; Elizabeth Ratcliffe; Anna Casey; - The COVID-19 Genomics UK (COG-UK) Consortium5; Joshua Quick; Alex Richter; Nicholas James Loman; Alan McNally.
Afiliação
  • Fiona Ashford; University of Birmingham
  • Angus Best; University of Birmingham
  • Steven Dunn; University of Birmingham
  • Zahra Ahmed; University of Birmingham
  • Henna Siddiqui; University of Birmingham
  • Jordan Melville; University of Birmingham
  • Samuel Wilkinson; University of Birmingham
  • Jeremy Mirza; University of Birmingham
  • Nicola Cumley; University of Birmingham
  • Joanna Stockton; University of Birmingham
  • Jack Ferguson; University of Birmingham
  • Lucy Wheatley; University of Birmingham
  • Elizabeth Ratcliffe; University Hospital Birmingham
  • Anna Casey; University Hospital Birmingham
  • - The COVID-19 Genomics UK (COG-UK) Consortium5; -
  • Joshua Quick; University of Birmingham
  • Alex Richter; University of Birmingham
  • Nicholas James Loman; University of Birmingham
  • Alan McNally; University of Birmingham
Preprint em En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21266297
ABSTRACT
Genome sequencing is a powerful tool for identifying SARS-CoV-2 variant lineages, however there can be limitations due to sequence drop-out when used to identify specific key mutations. Recently, Thermo Fisher Scientific have developed genotyping assays to help bridge the gap between testing capacity and sequencing capability to generate real-time genotyping results based on specific variants. Over a 6-week period during the months of April and May 2021, we set out to assess the Thermo Fisher TaqMan Mutation Panel Genotyping Assay, initially for three mutations of concern and then an additional two mutations of concern, against SARS-CoV-2 positive clinical samples and the corresponding COG-UK sequencing data. We demonstrate that genotyping is a powerful in-depth technique for identifying specific mutations, an excellent complement to genome sequencing and has real clinical health value potential allowing laboratories to report and action variants of concern much quicker.
Licença
cc_by
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: 1 Coleções: 09-preprints Base de dados: PREPRINT-MEDRXIV Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Preprint