MY GENE SCREEN
Find the right patients.
My Gene Screen is a pre-test eligibility assessment that clinicians or patients complete based on personal and family health history, compared against current national guidelines. It identifies patients who meet criteria for hereditary cancer genetic testing before an order is placed — so testing happens for the right patients, at the right time, without requiring a genetic counselor for every encounter.
SCALES YOUR TESTING PROGRAM WITHOUT ADDING STAFF
My Gene Screen runs inside your existing clinical workflow — in the EHR, at the lab intake point, or as a patient-facing intake tool. Clinicians get a clear eligibility output based on current guidelines. Patients arrive to appointments already screened. Providers focus on patients who need them most.
CONNECTS TO THE FULL CARE PATHWAY
My Gene Screen is the front end of a closed-loop platform. Patients who qualify for testing receive Living Lab Reports® when results are returned, and Genetic Alerts when science evolves. Identification doesn’t end at the order — it begins there.
BUILT ON CURRENT GUIDELINES, MAINTAINED AS THEY CHANGE
Eligibility criteria change. National guidelines updates. New genes are added. My Gene Screen reflects current guidelines so your referring clinicians and intake workflows aren’t making decisions based on outdated criteria.
HOW HEALTH SYSTEMS ARE USING MY GENE COUNSEL
- A large health system is expanding its hereditary cancer testing program and needs to screen more patients without increasing genetic counselor workload.
- A large practice has moved to physician-initiated genetic testing and needs clinical decision support, standardized patient education, and ongoing updates.
- A cancer center wants to standardize paired somatic and germline testing and needs clinical support and patient education when results are returned.
- A medical center is offering NIPT to all pregnant women and needs a scalable way to deliver pre-test education and results — without adding genetic counseling staff.
The conversations I have with patients about genetics are the hardest. This is an amazing resource that arms clinicians with the necesssary knowledge to have those conversations and ensure patients are getting consistent, expert care.