I-WGS (NGS)

Ukulandelana kabusha kwe-genome ephelele nge-Illumina noma i-DNBSEQ kuyindlela ethandwayo yokuhlonza izinhlobo ze-genomic, okuhlanganisa i-single nucleotide polymorphisms (SNPs), izinhlobo zesakhiwo (ama-SV), kanye nokwehluka kwenombolo yokukopisha (ama-CNV). Ipayipi le-BMKCloud WGS (NGS) lisetshenziswa kalula ngezinyathelo ezimbalwa, kusetshenziswa i-genome yokubhekisela esezingeni eliphezulu futhi enezincazelo ezinhle ukuhlonza izinhlobo ze-genomic. Ngemva kokulawulwa kwekhwalithi, ukufunda kuhambisana ne-genome yokubhekisela futhi izinhlobo ziyahlonzwa. Umphumela wazo wokusebenza ubikezelwa ngokuchaza ukulandelana kwekhodi okuhambisanayo (ama-CDS).