07 / GEN
Clinical Genomics
Clinical-grade genomics. Consistent, auditable, at scale.
From secondary analysis through variant classification and reporting, aligned to ACMG/AMP standards, tuned for high-throughput clinical labs, and ready for regulated environments.
[ Overview ]
What we do
for your team.
Genomic testing shouldn't depend on which analyst reviewed the case. Our platforms standardize evidence gathering and classification while preserving expert judgment where it matters.
Every reported variant carries a full evidence chain: predictions, population data, literature, and prior interpretations. Reviewable, exportable, and defensible.
DiagnosticsClinical LabsBiopharma
[ Capabilities ]
- Germline & somatic variant calling at scale
- ACMG/AMP-aligned classification workflows
- Structural variant, CNV & fusion analysis
- Pharmacogenomics interpretation and reporting
- Clinical report generation with full evidence chains
[ Outcomes ]
- 01
Faster turnaround for diagnostic and clinical labs
- 02
Consistent interpretations across analysts and sites
- 03
Auditable evidence chains for every variant call