21/01/2026
Key Features of BGI cWES (Clinical Whole Exome Sequencing)
💡Comprehensive Gene Coverage: Sequences over 180,000 exons, covering ~22,000 genes, to find disease-causing mutations.
💡Technology: Utilizes BGI's DNBseq™ platform (combining cPAS, RCR, and DNBs) for high accuracy.
💡Variant Detection: Identifies Single Nucleotide Variants (SNVs), Insertions/Deletions (Indels), Copy Number Variations (CNVs), Aneuploidy, and mitochondrial variants.
💡Clinical Focus: Designed for rare genetic disorders and complex diseases, aiding in diagnosis and personalized treatment.
💡Data & Reporting: Provides raw data and offers standard/custom bioinformatics for analysis, with quality guaranteed.
Contact us immediately to learn more.