Step 01 — Sequence
From blood draw to base pairs in hours
Our CLIA-certified laboratory processes samples using Illumina NovaSeq X Plus, achieving 30x whole genome coverage with industry-leading turnaround times.
- Whole genome sequencing — 3.2 billion base pairs
- RNA sequencing for gene expression analysis
- Methylation profiling for epigenetic insights
- Structural variant detection at single-nucleotide resolution
Step 02 — Analyze
AI that thinks like a geneticist
Our proprietary Helix Neural Engine is trained on 14 million sequenced genomes and 40 years of clinical outcomes data. It detects patterns invisible to human review.
- Variant classification across 8 pathogenicity tiers
- Drug-gene interaction prediction for 3,200+ medications
- Polygenic risk scoring for 50+ complex traits
- Rare disease differential with 98.7% sensitivity
Step 03 — Act
Clinical reports that drive decisions
Helix reports integrate directly into Epic and Cerner workflows, surfacing genetic insights at the point of care — when they matter most.
- EHR-integrated variant alerts and clinical flags
- Pharmacogenomic dosing recommendations
- Cascade testing guidance for at-risk family members
- Patient-facing summary reports in 14 languages