Genomics
Blood shows how you're doing now. Your DNA shows what you're predisposed to over a lifetime. Sequenced once, it personalizes every protocol we ever build for you.
Talk to us about genomics How it works
Run via accredited partner labs · onboarding during your consultation
Why sequence your genome
For many conditions, your genome explains more of your lifetime risk than any lifestyle factor. It lets us act years earlier, not after diagnosis.
Gene variants change how you metabolize statins, caffeine, B-vitamins and more. We use this to choose what actually works for you.
Your genome doesn't change, so you read it once. Every subsequent 90-day cycle is more precise because of it.
Most polygenic risk scores were trained on European-ancestry data. We interpret yours with South Asian risk patterns in mind.
How it works
We confirm fit and arrange sequencing through an accredited partner lab.
A simple saliva or blood collection, no clinic visit required.
Whole-genome sequencing, then interpreted through our open engine and reviewed for safety.
Risk, pharmacogenomics and gene-informed protocol changes, in plain language. Yours to keep.
We read your DNA against your live biomarkers, so the protocol reflects both what you're predisposed to and what's happening right now.