Coverage
Exactly what the report reads — and what your chip can’t see.
The report reads your DNA file across sixteen areas, then annotates what it finds from public, peer-reviewed databases. Every lookup runs against our own copies of those databases, and all of it is honest about its limits.
~600–700k
positions directly genotyped
A consumer chip reads a fixed set of SNPs — a tiny, deliberately-chosen slice of the genome.
~70M
variants after imputation
Indaga imputes to a reference genome (Beagle + the 1000 Genomes 30× panel), reaching tens of millions of variants — with quality scores kept and surfaced.
callable / not
stated for every finding
Where a position can’t be trusted from your file, it’s reported as not callable — never as “you’re fine.”
What the report reads
Sixteen areas, in six groups.
Fourteen wellness areas, where each reading names the gene behind it and how it was read, and two panels, where on a chip “not read” is most of the story: written down, never guessed.
- Cellular
- Methylation · Detox and histamine · Immunity · Longevity
- Systems
- Hormones · Mood and focus · Sleep and body clock · Senses · Skin and hair
- Heart and metabolism
- Heart and lipids · Blood sugar and liver
- Nutrients
- Food and vitamins · Gut and digestion
- Activity
- Training and recovery
- Panels
- Hereditary-cancer genes (not interpreted) · How your genes may affect some medicines
The report does not interpret the hereditary-cancer genes. A chip carries common sites in them, but the rare changes that matter mostly lie elsewhere, and only clinical sequencing reads those reliably. Medicine results are preliminary: a clinical test must confirm one before any medical decision. Never start, stop or change a medicine because of your DNA. Ask your doctor or pharmacist.
Annotation sources
Public databases, downloaded once and queried in-house.
Every interpretation is grounded in named, public, peer-reviewed sources. We download them once and query our own copies on our server, so your individual genes are never looked up in someone else’s database.
- ClinVar
- gnomAD (gene constraint)
- PGS Catalog
- GWAS Catalog
- AlphaMissense
- REVEL
- MANE Select
- GenCC + ClinGen
- PanelApp
- Reactome
- Human Protein Atlas
- Gene Ontology
- 1000 Genomes
- ExAC + GO-ESP (frequencies)
Indaga provides longevity and wellness information, not medical advice or a diagnosis. Its insights are designed to be reviewed with a qualified clinician.
Indaga is in active development.
We’re building it privacy-first, cited, and honest about what it can and can’t see.
Free: what your file covers and five trait readings (lactose, alcohol flush, caffeine sensitivity, skin and sun, muscle fibre). $69: the full report and the full analysis. No card needed for the free report.