Related Experiment Video
Updated: Nov 20, 2025

Quantification and Whole Genome Characterization of SARS-CoV-2 RNA in Wastewater and Air Samples
Published on: June 30, 2023
Partial N Gene Sequencing for SARS-CoV-2 Verification and Pathway Tracing.
Sin Hang Lee1, Jonathan McGrath2, Stephen P Connolly2
1Milford Molecular Diagnostics Laboratory, Milford, CT, USA.
Sequencing SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) nucleocapsid gene amplicons can confirm positive RT-qPCR results and track virus strains. This method helps reduce false positives, preventing unnecessary disruptions from inaccurate COVID-19 diagnoses.
Area of Science:
- Virology
- Genetics
- Public Health
Background:
- Real-time quantitative polymerase chain reaction (RT-qPCR) tests for SARS-CoV-2 can yield false positives, especially during periods of low virus prevalence.
- Accurate confirmation of positive results is crucial for effective disease management and preventing unnecessary public health measures.
Observation:
- A case of mild COVID-19 was confirmed using partial sequencing of the SARS-CoV-2 nucleocapsid (N) gene.
- The sequencing identified a specific mutation pattern (GGG-to-AAC) linked to strains originating in Continental Europe.
- Re-testing reference samples revealed mutations, including one associated with New York state strains and a novel frameshift mutation.
Findings:
- Partial N gene sequencing accurately verifies SARS-CoV-2 positive RT-qPCR results.
- The method can differentiate between various SARS-CoV-2 strains, aiding in tracking virus transmission.
- Identified mutations included known European and New York variants, as well as a novel insertion.
Implications:
- Routine sequencing of RT-qPCR positive samples can significantly reduce false-positive diagnoses.
- Minimizing false positives can prevent undue public anxiety and avoid unnecessary closures of schools and businesses.
- This approach supports more reliable monitoring of SARS-CoV-2 strain movement and evolution.
More Related Videos
09:34Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
09:33Author Spotlight: Finding New Therapeutic Targets for Malignant Peripheral Nerve Sheath Tumor Through Genome-Scale shRNA Screens
Published on: August 25, 2023
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
Sanger Sequencing