How it works

Upload. Analyse. Delivered.

A high-throughput pipeline turns your raw genomic file into a clinical-grade report inside an 8 to 12 hour window, 99% of the time.

Processing begins on receipt, no queue

1

Secure upload

Drop your raw file into the portal. It's encrypted in transit and at rest the moment it arrives, keyed to your account. No one browses your data.

2

Automated pipeline

Validated bioinformatic pipelines parse, quality-check, and call your variants, then score them against curated clinical and population reference databases.

3

Report + export

You receive an encrypted PDF report and a structured JSON/CSV export in your portal, with the AI Assistant unlocked on the Max Plan.

Accepted formats

Bring a file from any major provider

Consumer genotype exports, clinical VCFs, and raw sequence reads are all supported.

.txt .csv .vcf .fastq .zip

Have an unusual format or a very large file? Check with us first ›

The deliverables

What lands in your portal

Each tier adds a file. The Max Plan delivers all three plus the AI engine.

File 01
BasicAdvancedMax

Advanced Genome File

Encrypted PDF · JSON · CSV · ~36 pages

Encrypted PDF report plus a structured raw export (JSON/CSV). Your foundational read.

  • Primary genetic traits
  • General wellness indicators
  • Carrier status highlights
  • Basic metabolic gene variant calls
Your snapshot 434,818 SNPs 🩸 A (A/O) BLOOD TYPE 👁️ Brown EYE COLOUR 🌅 Early bird BODY CLOCK 🥛 Intolerant DAIRY 🧬 Slow (MTHFR) FOLATE 💊 Sensitive STATINS
Sample: your trait snapshot
File 02
AdvancedMax

Advanced Medical File

Adds ~18 clinical pages · ClinVar + PharmGKB sourced

Specialised clinical-grade medical analysis layered on top of the genome file.

  • Pharmacogenomic profiling (drug–gene)
  • Hereditary disease risk assessment
  • Cardiovascular markers
  • Oncological risk factors
  • Actionable clinical & lifestyle summaries
PHARMACOGENOMICS METABOLISER STATUS BY GENE CYP2D6 NORMAL CYP2C19 POOR SLCO1B1 RAPID CARDIO RISK 72nd pct
Sample: pharmacogenomics panel
File 03
Max only

Gene Integration File

Polygenic model · cross-system synthesis

Cross-functional biological analysis evaluating how multiple variants interact synergistically across systems.

  • Polygenic interaction scoring
  • Cross-system trait synthesis
  • Combined-risk interpretation
INTEGRATION MAP APOE LDLR PCSK9 TCF7L2 FTO CARDIO-METABOLIC CLUSTER · 5 LOCI
Sample: variant interaction map
File 04
Max only

Interactive Health AI Engine

Conversational · cited to source · HIPAA-compliant

A HIPAA-compliant conversational interface that reads your genomic reports alongside uploaded lab results.

  • Blood panel, CBC & lipid ingestion
  • Genotype-aware answers in real time
  • Cited to the exact variant or marker
HEALTH AI LIVE SOURCE · rs762551 Ask about your results...
Sample: assistant with cited sources
8–12 hours away

Pick a tier and upload your file.

Your report is waiting in the portal before the window closes.