01 / YOUR BIOLOGY
See the connections.
The systems behind your signals, explained in language you can use.
The Indaga genome report
Your DNA.
Made meaningful.
A beautifully readable account of your biology. What your genes can tell you, what your file couldn’t read, and a thoughtful place to begin.
01A personal plan
02The science behind your story
03Every blind spot, in plain sight
From your existing MyHeritage, AncestryDNA or 23andMe file.
INDAGATHE GENOME REPORT
The story of you.
Your genome, read honestly.DESIGN PREVIEW · NO PERSONAL DATA01
Explore the edition
A closer look
A little more understanding.
A useful next step.
Move from your biology to your everyday life, with space to understand what each finding actually means.
02 / YOUR EVERYDAY
Make it practical.
Food, habits and the blood tests that turn a tendency into a measured value.
03 / YOUR PLAN
Know where to begin.
Nine things your measured genotypes support, with the reasoning close by.
The complete edition
Seven chapters.
One connected story.
From the first page to the references. Explore what each section contains.
01Your plan+
Nine things your measured genotypes support, and the blood tests that would say more.
02Where your signal sits+
Every area on one page, in a fixed order, with its state and how much of it was read.
03Your story+
One page for each group of your biology: what it is, what your genes say, and what you can do.
04Genes by area+
The appendix: the genes the plan and the story rest on, with variant, your letters, how each was read and the evidence.
05Not on this file+
The markers this chip could not read, and why — listed, never guessed.
06How we read it+
The method, the rule behind every state, a glossary and the references.
07Closing+
The first steps, what to bring to a practitioner, and when this report changes.
The way we read
Clarity includes
what we don’t know.
Your DNA describes tendencies. The report keeps that distinction visible on every page.
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”.
Already tested? Start here.
One file.
A fresh perspective.
Download the raw-data file from your DNA provider. You don’t need a new kit.
Original .txt, .csv or .zip · up to 64 MB
MyHeritageFully supported+
DNA → Manage DNA kits → the three dots beside your kit → Download. The link arrives by email.
AncestryDNAFully supported+
Download your raw DNA data from your account settings.
23andMeFully supported+
Download your raw DNA data from your account settings.
Your next chapter
Your story starts here.
The report begins with your DNA file. Your questions can keep growing from there.
- 01
Get your DNA file
From your DNA service, as above.
- 02
Wait for checkout to open
- 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.
The full genome report
Checkout opens shortly.
We’re preparing the next release. In the meantime, explore the interactive sample.
Explore the on-screen sampleThe interactive sample uses a synthetic person.
Beyond the page
Keep the conversation
going.
Connect your own AI to the same record behind your report. Ask a new question and follow it back to the evidence.
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.
Connect your AI via MCP
Parts of your record, including genetic data, go to your AI’s provider under its terms. You choose whether to connect.
Longevity and wellness information, never a diagnosis. A measured value always outranks a genetic tendency. Your record is yours: the iOS app can erase your analysed record; deletion on the web and removal of the uploaded file require a request.