WGS (NGS)

Totum Genome rursus sequencing cum Illumina vel DNBSEQ est vulgaris modum ad identifying genomic variants, comprehendo una nucleotide polymorphisms (Snps), structural variants (SVS), et copy pluribus variants (SVS), et copy pluribus variants (SVS) et copy variants (CNVS). Et BMKCloud WGS (NGS) Pipeline facile deployed in paucis gradus, usura summus qualitas et bene-annotated reference genome ad identify genomic variants. Post qualis imperium, legit sunt aligned ad reference Genome et variants sunt identified. Effectus eorum eget praedicitur per annotating correspondentes coding sequentia (CDS).