Structured genetic research reports for clinical use
Help your patients understand their genetic findings with a structured, cited research summary they can review alongside your clinical guidance.
How clinicians use Geneformation
Save time preparing for consultations and empower your patients with accessible, structured information.
Pre-consultation preparation
Quickly review a structured summary of published research, clinical trials, and relevant experts before meeting with a patient or family.
Patient and family education
Provide families with a structured, plain-language report they can review at their own pace, with linked sources for further reading.
Research landscape overview
Get a current snapshot of the treatment landscape, active clinical trials, and key researchers for a specific gene or variant.
What each report includes
Every report is structured to support both clinical review and patient comprehension.
Gene overview and function
Summary of gene function and associated conditions.
Variant-specific findings
Published research linked to the specific variant.
Treatment landscape
Clinical trials, therapeutic approaches, and pipeline research.
Relevant clinicians and researchers
Curated list of experts with publication links.
Family-friendly summary
Plain-language overview patients can share with family.
Registries and communities
Patient groups and support organizations.
Full citations and sources
Claims linked to their sources, with full citations.
Downloadable PDF
Professionally formatted PDF for clinical appointments.
Why clinicians choose Geneformation
Cited, not generated
Findings link to the sources they draw on.
Dated and verifiable
Each report includes its generation date and links to original sources, so you can verify currency and accuracy.
Patient-ready formats
Online report dashboard for easy access plus a professionally formatted PDF patients can bring to appointments.
Family summaries in plain language
Includes a plain-language summary designed for patients and family members to understand without a science background.
In their words
Immediately after receiving a diagnosis, feeling overwhelmed and alone, we were able to run a report on Geneformation and understand what research was already out there and how we could progress it further. It gave us a foundation from which we were able to take action, and instead of feeling helpless, we were able to identify a path forward.
It turns a variant into a world. Reading the report, I recognized the first 15 to 20 hours of my own effort, already assembled. It compresses the distance between ‘we found a mutation’ and ‘here is what is known,’ which can otherwise take months of a physician’s time.
Geneformation is an exceptional resource for families, researchers, and clinicians alike. I used it to analyze cases studied in my own lab and was amazed that, in less than an hour, it produced a comprehensive summary that saved many hours of literature review and even uncovered an important publication I had missed. It has the potential to become an invaluable tool for advancing rare disease research and patient care.
Shared with permission. Educational research support — not medical advice, and not a description of any medical outcome.
Ready to try it for your practice?
Generate a single report, or contact us about institutional and volume pricing.
Educational Research Support Only
Geneformation reports are educational research summaries. They are not a substitute for clinical judgment, diagnostic testing, or professional medical advice. Reports should be reviewed in the context of the patient's full clinical history.