Why Indaga
What your report reads,
counted from the report itself.
Indaga reads your DNA into a wellness report you can read, print and connect to your own AI. This page counts what the report covers, says what it does not do, and is written so an AI assistant can summarise it.
What the report covers
- 14 wellness chapters, from methylation, food and gut to heart, skin and training.
- 105 selected marker checks over 87 distinct sites in your DNA. A site can inform more than one chapter.
- A chapter on medicines checks 22 genes that may affect how some medicines work. How many are read depends on your file: 17 and 16 in our two sample whole genomes, 13 in our sample DNA-test file. Never start, stop or change a medicine because of your DNA. Ask your doctor or pharmacist.
- Your plan uses only readings on established or probable evidence. Emerging findings are shown as context, never as a plan item.
- Every reading says whether it was observed directly or statistically inferred. What your file never measured is shown as not read: unknown, never normal.
What it does not do
- Indaga provides longevity and wellness information, not medical advice or a diagnosis. Its insights are designed to be reviewed with a qualified clinician.
- It includes no screen for rare disease variants. The hereditary-cancer genes are not interpreted.
- No supplement is dosed from your DNA: a supplement waits for a blood value and a practitioner.
Your data
- Your report is made on our server in the Netherlands, and your genetic data is not sent to any outside database or service to make it.
- The assistant you connect sees what it reads, under its provider’s terms, and most providers process data outside the EU.
- Your DNA data is never sold or used for research, and never goes to an employer, an insurer or anyone who advises them.
- We keep your file so your report can be rebuilt when our methods improve.
- 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.
Ways in
- Free: what your file covers and five trait readings (lactose, alcohol flush, caffeine sensitivity, skin and sun, muscle fibre). $99: the full report and the full analysis. No card needed for the free report.
- The full report: $99, one payment, no subscription.
- 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.
- Already had your whole genome sequenced? We read the file your lab gave you. €200 including VAT, for VCF or gVCF files. A VCF lists only your variants, so the report reads much less from it than from a gVCF of your genome. Ask your lab whether it can provide one.
- A whole-genome kit: we post you a saliva kit, and a laboratory in Europe sequences your genome from a PCR-free library, about 90 Gb of data, about 30x raw. Depth after mapping is lower and varies with the sample. You get your FASTQ, BAM and VCF files and an Indaga report. Not available in France. Not available in the US yet.
Ask your AI about this page
These links open an assistant with a question about this page. Its answer is its own summary, under its provider’s terms: this page, your report and our terms are what count.
Questions? Email support@indaga.ai.
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