Highlighting the Expertise Behind StrandOmics: Advancing Germline and Somatic Variant Classification
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.
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