The full report · first, your file
Get your DNA file.
Everything in the report is read from the raw-data file your DNA service already holds. Download it once — it is the only thing you bring.
Where the file is
Two services today, 23andMe soon.
MyHeritage
Fully supported
DNA → Manage DNA kits → the three dots beside your kit → Download. The link arrives by email.
AncestryDNA
Fully supported
Download your raw DNA data from your account settings.
23andMe
Not read yet
Download your raw data from your account settings. The app accepts the file today and reads it once 23andMe support is live.
Upload the file as it came — .txt, .csv or .zip, up to 64 MB.
The report
Your genome, read honestly.
Your genes are the instructions your body uses to build, run and repair itself. The report reads the common variation in those instructions from your consumer chip, fills in what the chip did not read where that can be done with confidence, and says plainly where it could not look. It is longevity and wellness information, never a diagnosis.
For anyone who has taken a consumer DNA test and wants to know what it actually read — and what it did not.
Marks, not grades.
Notable · Worth a look · Typical · Beneficial · Not read — each result on its own scale, never against other people. A colour never means good or bad.
“Not read” is printed, never guessed.
Where the chip has no site, other laboratories write the common version by default. This report writes “not read”, so you can tell the two apart.
A plan of nine things.
Food you would eat anyway, a habit or two, and the blood tests that turn a tendency into a number. We do not dose supplements from a chip.
Blood tests outrank genes.
A measured value always outranks a genotype. Where a blood test would say more, the report names it and shows your last value — or “none on file”.
Get it
Checkout opens shortly.
We can’t take your email just yet — check back soon.
Have a 23andMe file? Hold off for now — the app accepts it today but reads it only once 23andMe support is live.
- 01
Get your DNA file
From your DNA service, as above.
- 02
Pay
- 03
Sign in and upload
Sign in at app.indaga.ai/login and upload your file.
- 04
Read your report
On screen at app.indaga.ai — and the printed edition.
Contents
What’s in the report
- 1
Your plan
Nine things your measured genotypes support, and the blood tests that would say more.
- 2
Where your signal sits
Every area on one page, in a fixed order, with its state and how much of it was read.
- 3
Your story
One page for each group of your biology: what it is, what your genes say, and what you can do.
- 4
Genes by area
The appendix: the genes the plan and the story rest on, with variant, your letters, how each was read and the evidence.
- 5
Not on this file
The markers this chip could not read, and why — listed, never guessed.
- 6
How we read it
The method, the rule behind every state, a glossary and the references.
- 7
Closing
The first steps, what to bring to a practitioner, and when this report changes.
After the report
Keep asking — with your own AI.
Everything on the printed pages comes from the same record your assistant can read. Indaga speaks MCP, the open protocol AI assistants use to reach your data: point Claude, ChatGPT, Grok or any other assistant at your record and ask in your own words. The assistant does the talking; Indaga supplies the evidence and its limits.
Claude
One tap. Add Indaga to Claude, sign in to Indaga and approve. Set it up once and it follows your Claude account — the web, the desktop app and the phone.
ChatGPT, Grok and everything else
Any MCP client connects with the same address and the same sign-in. Paste it where your assistant asks for a server, choose OAuth, sign in and approve.
The command line
Claude Code, Codex, Gemini CLI and Antigravity take a credential instead of signing in. Create one at app.indaga.ai/connect and paste the config it gives you — the Indaga MCP server is then one entry in the tool's config.
Parts of your record, including genetic data, go to your AI’s provider under its terms — that is the trade-off, and we say so before anything is shared.
Longevity and wellness information, never medicine or a diagnosis. A result here is a tendency read from common variation; a measured value always outranks it. Your record is yours. Deleting it is not yet self-serve on the web: the iOS app can erase your analysed record, and removing the uploaded file is a request you make of us.