Predictive DNA Analysis

About Us


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.

Our Team


Cathy Tie


Chief Executive Officer

Twitter
Linkedin

Leo Wan


Chief Scientific Officer

Twitter
Linkedin

Scientific Advisory Board


Frederick Roth


PI at Roth Lab
University of Toronto

Song Sun


Postdoc Fellow
University of Toronto

Brian Naughton


Founding Scientist
23andMe

Board of Advisors


Karl Martin


CTO
Nymi Inc.

Mat Falkowsk


Founder
Invitae

Technology


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.


Partners

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.



Press

See What People Are Saying About Us



Careers

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].


Contact Us



  • University of Toronto
    27 King's College Cir
    Toronto, ON

  • SOS Ventures
    485 Jessie Street
    San Francisco, CA