Start with the patient’s genome
Explore the genetic information behind your patient’s questions, in the context of their individual record.
Genome Computer
for Clinicians
Bring your patient’s whole genome into care, with clinically relevant insights that stay current as the evidence changes.
Request accessFree whole genome sequencing for verified U.S. clinicians.
A new perspective
on every patient.
Bring genomes and other diagnostic results into one conversation.
Add other results for context
Bring other test results and reports into the conversation. View them alongside the patient’s genome to explore their genetic context.
Ask in your own words
Move from a patient record to a conversation. Explore findings, ask follow-up questions, and work through the details.
Genome Alerts
Be notified when something changes. Keep up with new evidence and changes in variant interpretation relevant to your patient’s genome, with context to help you decide what needs attention.
- Get notified about updated variant classifications.
- See what changed, why it matters, and suggested next steps.
- Ask follow-up questions and mark alerts as assessed.
Explore
Find a useful starting point in every genome. Choose a clinical question to open a patient-specific conversation, then explore the findings relevant to your care.
- Start with genetic risks, screening, and prevention.
- Explore medication response and cardiometabolic risk.
- Connect genetic context with lifestyle, labs, and ongoing monitoring.
Start with a better question.
Explore the questions that matter to your practice.
“What does this patient’s genome tell us about medication response?”
“What genetic context is relevant to these test results?”
“What evidence supports this finding, and what are its limitations?”
“Which findings should I look at more closely before our next appointment?”
For exploration and professional review. Always verify findings and supporting evidence before making clinical decisions.
Start with
your own genome.
We’re offering registered clinicians free whole-genome sequencing (WGS) and free access to Genome Clinic. Explore your own genome first, then see what’s possible for your patients.
- 01
Apply with your NPI
Share your professional details and individual National Provider Identifier for eligibility review.
- 02
Get your genome sequenced, free
Once approved, our team will help arrange your whole-genome sequencing.
- 03
Explore your own genome
Get free personal access to Clinic. Ask questions and experience the workspace for yourself.
Already have access? Sign in
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A few things to know.
Who is eligible for free sequencing and access?
Registered clinicians with an individual NPI (National Provider Identifier) can apply for free whole-genome sequencing and free Clinic access to test the workspace and explore their own genome first. Our team will review your professional details and NPI before arranging sequencing and access.
What is included in the offer?
Free whole-genome sequencing (WGS) of your own genome, plus free access to explore it in Genome Clinic. Get familiar with the experience yourself before considering it for your patients. We’ll discuss any patient sequencing or practice-wide access separately.
Why do I need to provide an NPI?
Your National Provider Identifier helps us review your professional details. Please provide your own 10-digit individual NPI, not your organization’s NPI. An NPI alone does not establish current licensure; our team reviews eligibility before onboarding.
What happens after I apply?
Our team will review your request and contact you at the email you provide. Once eligibility is confirmed, we’ll help arrange your free sequencing and personal access. Submitting this form does not automatically create an account, ship a kit, or grant access to patient data.
Do my patients need to have their genomes sequenced?
A patient’s genomic data is needed to explore their genome. If you already have sequencing data, or would like to discuss sequencing for your patients, let us know when you request access. We’ll help you understand the available options.
Can I add other results?
Yes. Add other test results and reports to the conversation to view them alongside the patient’s genome. Ask questions about their genetic context and explore how they relate to the wider clinical picture.
How is patient access managed?
Genome Clinic requires sign-in. Within the workspace, clinicians can view the patient records assigned to them by their clinic. We’ll discuss your organization’s privacy and data requirements during onboarding.
Does Genome Clinic replace clinical judgment?
No. Genome Clinic supports exploration and review of genomic information. Clinicians remain responsible for interpreting findings, verifying evidence, and making care decisions in the context of the patient’s full clinical history.