Skip to content
  1. Home
  2. >Dev Page

pageHero

Redefining the standard of care

A guideline-driven genetic testing workflow that saves you time

Slide Lorem Ispum lorem

Closing the gap between patient history and clinical action

CTA Label

Closing the gap between patient history and clinical action

Relevant personal and family history can sometimes be difficult to surface within standard patient records, creating potential gaps in proactive care delivery. Our genetic risk assessment utilizes rules-based logic to systematically surface these individuals through digital patient intake, aligning patient data with national clinical guidelines, and ensuring that patients who meet the criteria are identified and their providers are equipped to initiate proactive, evidence-based care.

Ready to scale your precision health program?

Discover how streamlining identification of patients meeting clinical guidelines for genetic testing can help your team work at the top of their license and improve patient outcomes. Request a personalized demo to see our genetic risk assessment in action and explore the future of automated clinical genomics.

Redefining the standard of care

A guideline-driven genetic testing workflow that saves you time:

Rich text with image

Here you can add an image to this field

Helix research network summit

Here
image inner block

Parent Subsection

Subsection

First

Case study

The Helix Genetic Risk Assessment evaluates whether a patient meets published, guideline-based criteria for genetic testing based on patient-reported personal and family health history, applying criteria from the American Heart Association, Heart Rhythm Society, the American College of Cardiology, and other leading cardiovascular organizations. The assessment is not a diagnosis. Providers should independently review results and exercise clinical judgment before approving any test order. This assessment does not evaluate or guarantee eligibility for insurance coverage, reimbursement, or payment for genetic testing