UNEXPLAINED SYMPTOMS
Your results came back normal. The answer may be in your DNA.
When blood work, imaging, and specialist visits haven't provided answers, whole genome sequencing looks where standard tests can't — across your entire genetic code — to uncover the root cause of unexplained symptoms.
What We Screen
The conditions standard tests miss.
Real Outcomes
Answers that changed lives.
Why Whole Genome
More than a test. A permanent health resource.
Your full DNA, not a panel
Gene panels test 50–500 genes. Whole genome sequencing reads all 20,000+ genes and the regulatory regions between them — nothing is excluded.
810+ clinical reports
Every test generates 810+ physician-ready reports covering hereditary risk, carrier status, pharmacogenomics, and more — all from a single sample.
Your test gets smarter over time
As new gene-disease associations are published, your stored genome data can be re-analysed. You sequence once and benefit from every future discovery.
The Process
Four steps to get started. No clinic visit required.
Order your kit
Free delivery worldwide.
Collect your sample
Simple finger-prick blood spot collection at home. Takes 5 minutes. Everything you need is in the kit.
Send it back
Pre-paid return label included. Drop it in any post box.
Access your results
Reports delivered to your Genome Manager in 6–8 weeks. Review every finding and share directly with your physician.
One test. A lifetime of answers.
One kit, sent to your home. Your entire genome sequenced at the clinical standard used for diagnostic decisions. 810+ physician-ready reports with Premium, delivered to your Genome Manager in 6–8 weeks — permanent and updated as science advances.
Free shipping · Results in 6–8 weeks
