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Volume 27, Number 5—May 2021
Research

Monitoring SARS-CoV-2 Circulation and Diversity through Community Wastewater Sequencing, the Netherlands and Belgium

Ray Izquierdo-Lara, Goffe Elsinga, Leo Heijnen, Bas B. Oude Munnink, Claudia M.E. Schapendonk, David Nieuwenhuijse, Matthijs Kon, Lu Lu, Frank M. Aarestrup, Samantha Lycett, Gertjan Medema1, Marion P.G. Koopmans1, and Miranda de Graaf1Comments to Author 
Author affiliations: Erasmus University Medical Center, Rotterdam, the Netherlands (R. Izquierdo-Lara, B.B. Oude Munnink, C.M.E. Schapendonk, D. Nieuwenhuijse, M. Kon, M.P.G. Koopmans, M. de Graaf); KWR Water Research Institute, Nieuwegein, the Netherlands (G. Elsinga, L. Heijnen, G. Medema); University of Edinburgh, Edinburgh, Scotland, UK (L. Lu, S. Lycett); Technical University of Denmark, Kongens Lyngby, Denmark (F.M. Aarestrup)

Main Article

Figure 1

Quantitative reverse transcription PCR Ct of severe acute respiratory syndrome coronavirus 2 RNA in sewage samples as determined by N gene (N1–N3) and E gene assays against the percentage of genome covered (>10×) by nanopore reads, the Netherlands and Belgium. A) N1 gene; B) N2 gene; C) N3 gene; D) E gene. Ct, cycle threshold.

Figure 1. Quantitative reverse transcription PCR Ct of severe acute respiratory syndrome coronavirus 2 RNA in sewage samples as determined by N gene (N1–N3) and E gene assays against the percentage of genome covered (>10×) by nanopore reads, the Netherlands and Belgium. A) N1 gene; B) N2 gene; C) N3 gene; D) E gene. Ct, cycle threshold.

Main Article

1These senior authors contributed equally to this article.

Page created: March 02, 2021
Page updated: April 20, 2021
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