How it works
From scattered data to a daily edge.
Indaga runs the same class of open-source tools and public scientific databases that academic labs use — assembled into one engine, made daily, and kept on your machine.
Step 1 — what you bring
Start with the file you already have.
Tens of millions of people already took a DNA test and never got much from it. Bring that raw file — no new kit, no upload. Add your Watch, glucose and lab panels whenever you like; each one makes the picture sharper.
DNA file
23andMe · MyHeritage · AncestryDNA · VCF
Wearable
Apple Watch · sleep · HR · HRV
Glucose
Dexcom / CGM sessions
Blood panels
lab PDFs, structured
- 23andMeraw data (.txt / .zip)
- MyHeritageraw DNA export
- AncestryDNAraw DNA export
- VCF / gVCFsequencing output
The four stages
Connect, pulse, synthesize, optimize.
- 01
Connect & ingest
Bring the DNA file you already have, and connect your Watch, CGM and blood panels. Everything is structured into your private Healthlake — on your machine.
- 02
Daily pulse
Each morning your sleep and activity update your Biological Clock and locate your Biological Midnight, using a validated 2025 cosinor heart-rate method.
- 03
Deep synthesis
A multi-agent loop — a drafter, an adversarial reviewer that hunts overstated claims, and a reconciler — reads your DNA and history to unlock the “why”.
- 04
Optimize
You get today’s levers, the contextual glucose view, an ask-anything explorer, and a doctor-ready letter for your next visit. Every claim traces to a named source.
Every claim traces back to a named public source — and to a record in your own Healthlake. If you want to check our work, you can.
Be first in line.
Indaga is in active development. Join the waitlist for early access and occasional, substance-only updates.