Context
A genomics-focused client needed a platform to bring together sequencing data, pipelines, and clinical interpretation into a workflow that could support diagnostics and decision making.
Our Role
- Documented user roles and scenarios for lab scientists, bioinformaticians, and clinicians.
- Specified requirements for data ingestion, pipelines, variant interpretation, and reporting.
- Structured user stories around typical diagnostic journeys and review steps.
- Created UI/UX mockups for variant review, reporting, and collaboration.
Outcome
The resulting documentation allowed the client to scope and prioritize an MVP that was realistic to implement while still supporting critical clinical workflows and regulatory expectations.
Original case study published on v-nomad.com.