Are you looking for...

- Efficient and user-friendly secondary analysis?
- Comprehensive variant interpretation and reporting according to professional guidelines?
- Standardizing your workflow from FastQ to report?

Invest 1 hour with us on these two variant days and see how you can take a step forward to improving your routine testing.

Whether you’re working with somatic cancer or hereditary disease, we have the solution to cure your data analysis and interpretation pains.