We are creating the world’s first comprehensive functional variant database solely dedicated to resolving variants of unknown significance (VUS) in genetic tests.
Our pipeline determines the functionality of all gene variants of any human disease gene using high-throughput genetic experiments.
Genetic testing companies can resolve their Variants of Unknown Significance (VUS) in our scientifically-proven database.
Proof of Concept
Using state-of-the-art high throughput genetic methodologies and next generation DNA sequencing technique, Ranomics has created a pipeline that helps you understand how your unique genetic makeup contributes to your health.
Please contact us if you or a rare disease patient you know would like our assistance. We are constantly on the outreach looking for new cases where we can positively impact rare disease patients’ and their families.
See What People Are Saying About Us
Ranomics is an early stage startup transforming personalized healthcare and genetic testing. If you are interested in joining our highly innovative and fast-paced environment, see the positions available below. Please send resumes to [email protected].