Curated clinical panels, a whole-genome pathogenic screen, and a graded interpretation universe — mapped, with every gene↔panel connection.
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named-panel genes
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genes shared across panels
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gene–disease validity
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polygenic scores
The genome coverage ring
Every panel and its sub-panels, sized by gene count. Hover a segment; click to expand its genes, provenance & source link.
Hover or click the ring
Panel provenance and gene list appear here. Center = de-duplicated union.
The gene ↔ panel network
The interconnection: bright nodes are hub genes shared across many panels. Hover to trace links; click a gene or panel to focus; drag to explore; search a gene.
shared genes onlyreset
Tip:hover MLH1 or COMT — they sit in 5 panels each.
Top hub genes — click to trace:
How the tiers overlap
The same gene often matters clinically and for wellness — one engine, all three tiers.
Chip vs sequencing — what the data can actually see
Coverage isn't one number. Chip+imputation is strong on common variants, near-blind on rare ones.
~90%
Chip · wellness layer
nutrigenetics · PGx · PGS · traits
~2%
Chip · rare-clinical
ACMG / carrier pathogenic (rare)
~99%
Sequencing (WES/WGS)
the honest upsell for the rest
Per-person coverage — measured, not assumed
On a panel ≠ callable in you ≠ a finding. Indaga screens broadly but reports, per person, which genes its data could read — “not measured” is never “negative.”