PT  - JOURNAL ARTICLE
AU  - Alexandra Rehn
AU  - Peter Braun
AU  - Mandy Knüpfer
AU  - Roman Wölfel
AU  - Markus H. Antwerpen
AU  - Mathias C. Walter
TI  - Catching SARS-CoV-2 by sequence hybridization: a comparative analysis
AID  - 10.1101/2021.02.05.429917
DP  - 2021 Jan 01
TA  - bioRxiv
PG  - 2021.02.05.429917
4099  - http://biorxiv.org/content/early/2021/02/10/2021.02.05.429917.short
4100  - http://biorxiv.org/content/early/2021/02/10/2021.02.05.429917.full
AB  - Controlling and monitoring the still ongoing SARS-CoV-2 pandemic regarding geographical distributions, evolution and emergence of new mutations of the SARS-CoV-2 virus is only possible due to continuous next-generation sequencing (NGS) and worldwide sequence data sharing. Efficient sequencing strategies enabling the retrieval of the maximum number of high quality, full-length genomes are hence indispensable. Here, we describe for the first time a combined approach of digital droplet PCR (ddPCR) and NGS to evaluate five commercially available sequence capture panels targeting SARS-CoV-2. In doing so, we were not only able to determine the most sensitive and specific capture panel, but to discriminate their mode of action and number of read pairs needed to recover a high quality full length genome. Thereby, we are providing essential information for all sequencing laboratories worldwide striving for maximizing the sequencing output and simultaneously minimizing time, costs and sequencing resources.Competing Interest StatementThe authors have declared no competing interest.