OUR MISSION is to help rare disease patients by ending their diagnostic odyssey.
Our research platform will let you and your provider look up all the known information about your diagnosed disease in minutes - related genes, repurposed drugs, existing care, and active clinical trials.
If you don't have a confirmed diagnosis, you may benefit from our free whole genome sequencing - a service we're proud to be the 1st in world to offer.
We are committed to you - all of our products and services will always remain free to patients, everywhere in the world.
Our platform is built to help you navigate the most challenging cases. Upload case information and uncover gene relationships, standards-of-care, and repurposed drug options in a few keystrokes.
Build fully referenced personalized care paths for your patients, and connect with global disease experts for Doctor : Doctor guidance.
We are committed to care - our platform is free to use for Research Clinicians and Care Teams anywhere in the world.
TMA will do the heavy lift upfront, so you can be sure the patients you're looking for have the genomic profiles you need.
For pre-clinical work, create customized datasets for pre-clinical research by accessing our database of deidentified paired patient data, comprised of whole genome sequences and comprehensive medical records.
