01
Understand the report
Explain terminology, inheritance language, evidence categories, and the stated limitations of the test.
Use Case
Genome
A careful path from difficult genetic reports toward useful, evidence-aware personalized health context.
What Lunas supports
- Plain-language genome report understanding
- Context across genetics, labs, medications, and history
- A phased path toward pharmacogenomics and evidence grading
The opportunity
Why this work needs medical context
Genetic data is becoming easier to obtain and harder to interpret. A consumer array, clinical panel, exome, and whole-genome sequence do not have the same coverage or meaning, and a reported variant is not automatically a diagnosis.
Lunas is building the interface between that complexity and the person who needs to understand it. The first useful step is report understanding: what was tested, what the report says, what remains uncertain, and what may be worth discussing with a genetics professional. Over time, genome context can sit alongside laboratory trends, medications, symptoms, and history to support more personalized questions.
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
Separate signal from uncertainty
Distinguish actionable findings from informational results and variants of uncertain significance.
03
Connect health context
Relate a report to relevant medications, laboratory values, symptoms, and family-history questions without claiming causation.
04
Prepare for expert review
Build a concise list of questions for a genetic counselor, pharmacist, or clinician.
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
Identify the test
Start with the test type, report source, sample date, and the limitations stated by the laboratory.
- 02
Review the findings
Use Stethos to explain the report language and preserve uncertainty.
- 03
Add relevant context
Compare the report with permitted medication, laboratory, symptom, and history information.
- 04
Confirm professionally
Use qualified genetics or clinical review before making health or medication decisions.
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
- Secure upload support for genome reports and permitted text/CSV data
- File-aware explanations in Lunas
- Early pharmacogenomics knowledge and human-review foundations
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
Does Lunas diagnose from DNA?
No. Lunas can assist with understanding a report, but it does not diagnose a person from genetic data.
Can Lunas tell me which medication to take?
No. Pharmacogenomic information may help frame questions, but prescribing and medication changes require a qualified professional who can consider the complete clinical picture.
Why does the type of genetic test matter?
Different tests examine different portions of the genome and have different limitations. A missing result on a consumer array, for example, does not prove that a variant is absent.
How is genetic data handled?
Genetic files are sensitive health data. Lunas uses private storage and controlled access, and deeper genome workflows are being phased alongside stronger genetic-data consent and retention controls.
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.