1Single query
Enter a variant
Type a gene plus HGVS, rsID, or genomic coordinate into the zero-trust search. Eamos normalises whatever you paste.
> RPE65 c.260A>G
parsed: NM_000329.3
normalised: chr1:g.68894…
Genomic intelligence platform
Instant, evidence-aggregated variant interpretation.
One variant in, one structured report out. Eamos aggregates ClinVar, gnomAD, SpliceAI, VEP, and PubMed into a single clinician-readable report — so you stop opening five tabs per variant.
Try
Eamos runs a live, parallel evidence aggregator across global genomics data.
0Tracked variants indexedacross the aggregated source graph
0Mined functional papersunique PMIDs, deduplicated
0Submissions to ClinVarpassed through the ledger messenger
Sample figures — live counters wire in at launch.
How it works
One variant in. One structured report out.
2Parallel sweep
Eamos queries every source at once
ClinVar, gnomAD, VEP, SpliceAI, and PubMed in parallel — aggregated and deduplicated, with the ACMG rules engine on top.
ClinVar … ok
gnomAD … ok
SpliceAI … ok
VEP … ok
3Instant rendering
Read the report
A clean four-card matrix with an AI-led summary, ACMG verdict, evidence table, and trials — every claim cited.
Verdict: Likely path.
PM1, PM2, PP3
Trials: 3 recruiting
Why Eamos
Built for the actual variant-interpretation workflow.
Eamos folds the databases you already open into one structured, cited, ACMG-aware report — engineered for speed and clinical trust.
Four-card evidence matrix
Population, splicing, functional, and consensus — the four pillars of evidence mapped cleanly above the fold, no nested tabs to dig through.
Cognitive summary generator
An immediate, conversational AI paragraph explains the biological verdict right below the matrix — with inline citations to every source.
Zero-trust aggregation
Records are pulled live, per query, over secure requests. No identifiable patient sequence files are ever stored on the platform.
Pass-through ClinVar messenger
Found a new functional assay? Wire it straight to ClinVar from your dashboard — no wrestling with complex federal submission forms.
From the bench · illustrative
Eamos completely changed our laboratory workflow. The dual-badge functional card alone saved our curation team over 100 hours of tedious manual review this year.
Dr Sarah Jenkins, PhDPrincipal Molecular Geneticist
Pricing
Start free. Scale to the whole lab.
Free
For individual research use.
$0forever free
Get started- Unlimited variant searches*
- Full variant evidence report
- 3 AI queries / day
- Community support
Most popular
Pro
For working clinicians and curators.
$9.95per month
Choose plan- 10 AI queries / day
- ClinVar & evidence submissions
- VCF upload (batch variants)
- Workbench — 1 active project
- Reclassification alerts & PDF export
Max
For power users and heavy workflows.
$24.95per month
Choose plan- Unlimited AI queries*
- Unlimited Workbench projects*
- Bulk VCF uploads*
- Priority support & evidence refresh
*Usage limits apply. Sample pricing — not final.
FAQ