Precision Genomics for Accurate Variant Classification

• Comprehensive Clinical Genomics Platform: StrandOmics provides end-to-end tertiary NGS analysis for both germline and somatic variant classification and interpretation.
• Proven Expertise: Successfully interpreted and reported over 30,000 germline cases for rare inherited disorders and hereditary cancer predisposition, and generated more than 10,000 somatic reports.
• Accurate and Reliable: StrandOmics ensures precise variant classification and reporting, supporting both germline and somatic analyses.