Complete viral genome sequencing is critical for identifying mutational variants that will impact research in the fields of virology, immunology, epidemiology, and molecular evolution, among others. However, maximizing viral RNA sequencing reads from clinical specimens or laboratory samples can be challenging, particularly due to the amount of host background RNA. Here, we present a targeted NGS strategy that pairs the Swift Biosciences RNA Library Kit with the Daicel Arbor Biosciences myBaits Expert SARS-CoV-2 kit with excellent enrichment sensitivity and specificity.
Application Note: Targeted Sequencing of SARS-CoV-2