01
Scan raw DNA
Turn a consumer export into readable findings instead of a wall of letters.
Use Case
Genome
Upload a consumer DNA export and get a readable report — including how your genes may affect common medications.
What Lunas supports
- Genome scan of consumer DNA raw-data exports
- CPIC pharmacogenomics: gene–drug interactions in plain language
- Genetic files stored privately, shared only by revocable grant
The opportunity
Why this work needs medical context
The raw-data file from a consumer DNA test sits in most people's downloads folder unopened — hundreds of thousands of rows of letters with no explanation. A clinical genetics report is the opposite problem: two pages of "heterozygous," "variant of uncertain significance," and "autosomal recessive" with no translator.
Lunas handles both. Upload the raw export and the genome scan works through it, surfacing findings worth knowing about — most usefully pharmacogenomics, built on CPIC guidelines: whether your genes suggest you may process certain common medications differently. Upload a clinical report and Stethos explains what was tested, what the language means, and what the lab itself says the test cannot rule out.
Genetics rarely stands alone, so findings live next to the rest of your record — lab trends, medications, history — and the most useful output is usually a short, informed list of questions for a professional.
Where Lunas fits
Useful work before the final decision
Stethos helps explain, organize, and investigate. People and qualified professionals stay responsible for the decisions that follow.
02
Check medications
See CPIC-based gene–drug notes worth raising with a pharmacist or prescriber.
03
Decode a report
Get "variant of uncertain significance" explained without the jargon.
04
Ask better questions
Walk into genetic counseling with a specific, prepared list.
A practical workflow
From a question to human review
A repeatable path makes the model easier to supervise and the result easier to trust.
- 01
Upload
Add your raw DNA export or a genetic report PDF.
- 02
Scan
Lunas processes the file and presents findings in plain language.
- 03
Understand limits
See what the test type can and can't tell you — a consumer array is not a whole genome.
- 04
Confirm professionally
Take medication-relevant findings to a pharmacist, counselor, or clinician before changing anything.
Product path
Start with Lunas today. Grow into governed workflows.
Lunas.One is available to individuals today. Team & Enterprise workspaces and a governed Stethos API are in active development — the roadmap below is directional, not a promise of present availability, and larger deployments will require the right privacy, security, evaluation, and human-review controls.
Available in Lunas
- Genome scan of consumer DNA raw-data exports
- CPIC-based pharmacogenomics findings
- Plain-language explanation of uploaded genetic reports
Team, Enterprise & API direction
- Deeper variant annotation and evidence grading
- Broader pharmacogenomics workflows
- Longitudinal personalized-medicine analysis under stronger consent controls
Questions
What people usually want to know
Can AI read my raw DNA data?
Yes. Download the raw-data export from your consumer DNA service and upload it to Lunas; the genome scan processes it and reports findings in plain language, including CPIC-based notes on how your genetics may affect common medications. Keep in mind a consumer array samples a small fraction of your genome, so a missing finding is not proof of absence.
Can my DNA tell me which medications work for me?
It can flag possibilities. CPIC pharmacogenomics links certain genes to how people process specific drugs, and Lunas surfaces those links from your data. But dose and drug choice depend on far more than one gene — never start, stop, or change a medication on your own; bring the finding to your prescriber instead.
Is it safe to upload my DNA to Lunas?
Genetic files are treated as the sensitive health data they are: private storage on HIPAA-ready infrastructure, BAAs with every vendor that touches health data, and access only through time-limited grants you create and can revoke.
Why does the type of genetic test matter?
A consumer array checks preselected positions; a clinical panel, exome, or whole genome each cover progressively more. A "no finding" on a narrow test doesn't mean the variant isn't there — Lunas states the limits of whichever file you upload.
Try the product
Bring one real health question into context.
Use Lunas for information and organization, then involve a qualified professional whenever a health decision is needed.