I-WGS (NGS)

Ukulandelana kabusha kwe-genome yonke ne-Illumina noma i-DNBSEQ kuyindlela edumile yokuhlonza okuhlukile kwe-genomic, okuhlanganisa ama-nucleotide polymorphisms (SNPs), okuhlukile kwesakhiwo (ama-SVs), nokuhluka kwenombolo yokukopisha (CNVs). Ipayipi le-BMKCloud WGS (NGS) lisetshenziswa kalula ngezinyathelo ezimbalwa, kusetshenziswa i-genome yereferensi yekhwalithi ephezulu nechazwe kahle ukukhomba okuhlukile kofuzo. Ngemuva kokulawula ikhwalithi, ukufundwa kuqondaniswe ne-reference genome futhi okuhlukile kuyahlonzwa. Umphumela wabo wokusebenza ubikezelwa ngokuchaza ukulandelana kwamakhodi okuhambisanayo (CDS).