Personal library
Reports, panels, documents, dates, labs, and notes in one persistent space.
Genomic companion
Your genetic information, organized for real conversations.
Pocket Genes turns reports, panels, and complex concepts into a personal space to review, learn, prepare questions, and share information carefully.
More than visualization
A beautiful report helps. An organized companion changes how information is used.
The mobile experience should show data clearly, but it also needs to answer practical questions: where is my report, what does this term mean, which genes did this panel cover, what should I review before seeing the specialist, and what can I share.
The personal companion organizes information in layers: documents, concepts, reported variants, history, notes, and next questions.
PDF+reports turned into navigable information
QAquestions prepared for appointments
Sharecontrolled sharing with relatives or professionals
Layers of the companion
Each layer responds to a concrete need during the genetic journey.
Contextual glossary
Explanations of variants, inheritance, penetrance, carrier status, pharmacogenomics, and sequencing.
Medical preparation
Question lists, open topics, and points to confirm with professionals.
Controlled sharing
Clear ways to share relevant information without losing privacy or context.
Understanding
Access to clear resources in difficult moments
Genetic information arrives loaded with technical terms. Pocket Genes should turn them into language people can review, trust, and return to.
Concepts in context
Explain terms when they appear, not in a separate library no one finds.
Separate certainty from uncertainty
Distinguish reported data, clinical interpretations, and questions that require a professional.
Family-friendly language
Help a parent, adult patient, or caregiver review essentials without genetics training.
Preparation
Better appointments, not automatic answers
The product should not promise diagnoses. It should help people arrive with the right material and more precise questions.
What to bring
Reports, dates, previous tests, background, and notes ready to share.
What to ask
Questions about genes not covered, reanalysis, relatives, inheritance, specialists, and next tests.
What to review after
Track answers, new indications, and recommended resources.
Responsible design
A genomic companion must be careful with language, privacy, and expectations. Clarity does not mean oversimplifying or making clinical promises.
- Avoids alarmist language.
- Keeps privacy as a central setting.
- Indicates when a question should be reviewed with a professional.
Trust requires structure
The value appears when information stops being scattered and starts supporting informed decisions with the medical team.