Read, not estimated.
A consumer chip measures selected positions, and the common variants it didn’t measure are estimated from a reference panel. A whole genome is read directly.
Whole-genome sequencing
Your whole genome, read honestly.
We post you a saliva kit and a laboratory in Europe reads your whole genome. Indaga turns it into one cited record: a report for you, and evidence your own AI can read, with what was never measured kept in view.
Already took a DNA test? Start with its file.
- Saliva kitPosted to you. You post your sample back.
- A lab in EuropeYour whole genome, about 90 Gb of data or more, PCR-free.
- Your filesFASTQ, BAM and VCF, yours to keep.
- Your AIClaude, ChatGPT or another assistant, over MCP.
Why a whole genome
A chip reads chosen spots. A genome reads the whole book.
A consumer DNA test reads selected positions, hundreds of thousands of them. Whole-genome sequencing reads your DNA itself: about three billion letters, nearly every gene from end to end.
Whole genes, not single spots.
No chip reads a whole gene. Sequencing covers nearly all of each gene, including the stretches a chip never looks at.
Your files, yours to keep.
FASTQ, BAM and VCF: about 90 Gb of data or more from a PCR-free library, in the standard formats genetics tools read.
Tested once.
Your genome doesn’t change. We keep the file so your report can be rebuilt when our methods improve.
The saliva kit
Your whole genome, read by a lab.
For a DNA reading without a file: we post you a saliva kit, and a lab reads your whole genome.
- You order.You sign in to Indaga and pay. Until your kit is posted, you can cancel for a full refund.
- We post you a saliva kit.Within 5 business days of your payment. We email you first to ask for your shipping address.
- You give a saliva sample.You follow the kit’s instructions and post your sample back.
- A laboratory in Europe reads your whole genome.
- You get your Indaga report and your data files.
From €749 including VAT
Available nowNot available in France. Not available in the US yet.
Already had your whole genome sequenced? We read the file your lab gave you.
Indaga Connect · MCP
Your record, read by your own AI.
Connect Claude, ChatGPT or another assistant to your record, then ask about your report in your own words. Included with the full report for as long as you have it, or €7 a month without it. The assistant you connect sees what it reads, under its provider’s terms, and most providers process data outside the EU.
What your AI is told
- What was never measured is unknown, never normal.
- Old values are quoted with their date.
- A percentile or a “Pathogenic” label is not a diagnosis.
- It cannot erase your whole record, export it or change your settings.
- 01
One record
Your genome becomes a small, structured record, not the raw file. Apple Health and blood results add context, in beta.
- 02
Add the connector
Claude, ChatGPT and Claude Code each sign in to Indaga with OAuth, over MCP at
app.indaga.ai/v1/mcp. - 03
Ask
The assistant asks Indaga for the evidence and answers in its own words, and can cite its sources.
Privacy
As little about you as we can.
Your record is yours. Every route says what it keeps, where, and who can see it.
An email is enough to sign in
We email you a code to sign in. For sign-in, we keep only your email address and an account ID, on our server in the Netherlands (EU).
Hosted in the Netherlands, encrypted on disk
We hold your record in a store of its own, on our server in the Netherlands (EU), encrypted on disk. There is no separate key per person, and we say so. You choose whether to connect an AI. Never sold, never used to train AI.
Delete it
To delete it, use “Withdraw consent and delete my DNA data” on your dashboard at app.indaga.ai, or email support@indaga.ai; we delete within 30 days.
It’s honest about uncertainty
Absence is never “normal.” A test you never took returns “not measured,” not “you’re fine.” We’d rather drop a finding than alarm you with a false one.
Research
We do research, and publish what we test.
Alongside the record, Indaga studies what DNA and AI can honestly say about health and aging. Research, never a diagnosis.
Human lives eight times longer. Eight years to find the way.
Our moonshot, and the research behind it. Nobody knows how yet, and nothing Indaga offers makes anyone live longer.
Read the moonshot
How honestly does an AI read DNA?
We test AI models on DNA questions whose answers are known, and publish the data on Hugging Face.
Our datasets
A second look, with the family’s doctor.
Research for families whose genetic tests came back negative or uncertain: all their data read again, together, with their doctor. Research, not diagnosis.
We’re looking for research partners: clinicians, laboratories and groups who study aging or rare disease. Write to support@indaga.ai.
Already tested? The DNA report
A report worth spending time with.
A clear plan, the biology behind it, and the evidence beneath every finding. Designed to be read, revisited and brought to a better conversation about your health.
- 01
Your next stepsOnly what your measured genotypes support.
- 02
Your biology, explainedFrom cellular processes to everyday habits.
- 03
The full picture, including the gapsEvery unread marker stays visible.
Start with the DNA file you already have.
INDAGATHE GENOME REPORT
The story of you.
Your genome, read honestly.DESIGN PREVIEW · NO PERSONAL DATA01
Explore the edition
Indaga
There’s a story in your biology.
Longevity and wellness information. Never a diagnosis.