“…Sanger sequencing was the first method used with variable size of amplified regions (St-Jean et al, 2004;Vijgen et al, 2005). Targeted viral nucleic acid capture and RNA sequencing library was recently used to sequence four human HCoV-OC43 isolates (Dinwiddie et al, 2018). The most usual method is to divide the genome into 2.5 kb regions which are amplified, fragmented and sequenced with HTS technologies (Cotten et al, 2013;Taboada et al, 2016).…”