Our digital tools help clinicians quickly gather family history, visualize pedigrees, and generate automated risk assessments that align with current guidelines. This allows providers to efficiently identify patients who qualify for genetic testing, improve referral accuracy, and ensure consistent documentation across the system.
The Living Lab Report® bridges the gap between genetic testing and clinical care by providing structured, evidence-based genetic counseling content tailored for both providers and patients. Designed to support informed decision-making, each report translates complex results into clear, actionable insights—enhancing clinical conversations and improving patient understanding at every step.
Guidelines, variant classifications, and medical management recommendations evolve rapidly — often across multiple specialties. My Gene Counsel’s Living Lab Reports® automate this process, continuously integrating new evidence so clinicians don’t have to track each change themselves. Our system ensures every provider and patient benefits from the most current data, reducing missed updates, saving time, and maintaining consistent, evidence-based care across the organization.
CLINICAL CARE SYSTEMS
We help partners efficiently deliver precision medicine at scale. By uniting family history collection, risk assessment and continuously updated Living Lab Reports, My Gene Counsel streamlines genetic testing workflows, reduces provider burden, and ensures every patient receives current, clinically actionable information.
I led the pilot implementation of My Gene Counsel digital tools at Tampa General Hospital to evaluate if this solution could help us scale our genetic counseling and testing operations. Over the 6-month pilot, we saw consistent improvements in percentage of eligible patients tested, and for certain cancer types, it took less time from diagnosis to genetic testing. The My Gene Counsel team was supportive and easy to work with, and they met us where we were in terms of workflow and staffing to make this pilot a success. With their help, we published our data and the team has expanded their efforts to use these tools to see more patients efficiently and effectively.