TREATMENT NOT WORKING
Your diagnosis may be right. Your treatment plan may be incomplete.
Many conditions have genetic subtypes that determine which therapies are effective. Without identifying the specific variant, treatment is guided by averages — not by your biology. Whole genome sequencing reveals the molecular detail your care team needs to refine the plan.
Genetic Subtypes
Same diagnosis. Different biology. Different treatment.
Oncology
Different genetic subtypes of the same cancer require entirely different drugs. A tumour's molecular signature — not just its location — determines which therapies will be effective.
Neurological
SCN1A mutations cause Dravet syndrome, where standard sodium-channel blockers can worsen seizures. Identifying the subtype changes the entire medication strategy.
Cardiac
Hypertrophic cardiomyopathy has dozens of causative variants, each with different risk profiles and management protocols. The wrong approach can be dangerous.
Pharmacogenomics
Your genome determines how you metabolise medications. Poor metabolisers may get no benefit; ultra-rapid metabolisers may experience toxicity at standard doses.
Why Whole Genome
The difference between a partial picture and the full one.
See every variant, not just the common ones
Targeted panels test for a pre-selected list of mutations. Whole genome sequencing reads all 6 billion base pairs — including rare and novel variants that panels miss entirely.
Connect your diagnosis to the right treatment
Many conditions have genetic subtypes that respond to different therapies. WGS identifies the specific variant driving your condition so your physician can match the treatment to the biology.
One test that never needs repeating
Your genome is sequenced once and stored permanently. As pharmacogenomic research advances and new gene-drug interactions are discovered, your data is re-analysed automatically.
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
