My Gene Counsel provides a digital platform that automates genetic risk assessment, counseling, and continuous result updates. It integrates web‑based family‑history intake, algorithmic risk scoring, and auto‑refreshing Living Lab Reports® via FHIR‑compatible APIs, enabling hospitals, clinicians, and biotech firms to embed scalable genomic counseling into EHRs and research workflows.
Funding
$500K raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Healthcare providers and researchers lack a scalable, digital system that delivers accurate, timely, and continuously updated genetic counseling for patients, leading to fragmented workflows, increased provider burden, and limited integration of genomic data into precision‑medicine initiatives.
Solution
My Gene Counsel offers an end‑to‑end digital platform that bridges genetic risk assessment, counseling, and ongoing result updates. The solution begins with a web‑based family‑history intake that applies validated algorithms to generate individualized risk scores. Results are delivered through Living Lab Reports® that automatically incorporate new scientific evidence, guideline revisions, and patient‑specific follow‑up data. A long‑term notification engine keeps patients informed of relevant updates and prompts re‑evaluation when needed. The platform provides APIs and FHIR‑compatible interfaces to embed these tools into electronic health records, clinical trial workflows, and biotech data pipelines, reducing manual effort and ensuring consistent, patient‑centric communication across the care continuum.
Target Audience
Primary customers are hospitals, health systems, and clinicians seeking to embed genetic counseling into routine care, as well as biotech, pharmaceutical, and research organizations that require scalable genomic data collection and patient engagement tools for trials and population studies.
Features
- Web‑based family‑history collection module with algorithmic risk stratification and carrier‑screening recommendations
- Living Lab Reports® that auto‑refresh with the latest genomic research, variant re‑classification, and clinical guidelines
- Automated long‑term notification system for post‑test follow‑up, new evidence alerts, and patient reminders
- Secure, HIPAA‑compliant data storage with role‑based access controls and end‑to‑end encryption
- FHIR‑compatible APIs and SDKs for seamless integration into EHRs, clinical trial management systems, and biotech data platforms
- Provider dashboard offering real‑time analytics, patient cohort views, and customizable reporting templates
- Scalable architecture supporting population‑level studies and high‑volume enrollment for research and drug development programs