L. Labriola, J. Ruelle, A. Scohy, F. Seghers, Q. Perlot, J. De Greef, C. Desmet, C. Romain, J. Cyr Yombi, H. Rodriguez-Villalobos, B. Kabamba, and M. Jadoul. Journal of Medical Virology, November 2021; Article link: doi:10.1002/jmv.27471.  This email address is being protected from spambots. You need JavaScript enabled to view it.

Citation: "... Fastq files were uploaded on the cloud-based ASP-IDNS®−5 analysis software (SmartGene). Analysis was made using [SmartGene's] ... Coronavirus pipeline .... Briefly, paired-end reads were generated and automatically filtered for low-quality sections. The resulting reads were mapped against the SARS-CoV-2 profiles and mutations were detected in a quantitative manner (% reads aligned). A consensus genome was generated using a 40% cut-off for base determination and a minimal number of 30 reads per position. ..."