My vision is to develop a tool to help the doctors make sense of the complex information in their patient’s DNA. More importantly, we need to make sure we give patients the tools to understand what this genetic information means for them.
For the first time in our history we can identify all of the genetic differences that make each one of us, us. The thing is, that each of us have so many differences that it’s incredibly hard to doctors to make sense of all this information. For your doctor to use the information in your DNA, we need to make it easier for them to interact with, and to do that, we’ve developed a tool that simplifies this complexity. This is a modern day genome browser. This is something for doctors and patients. This is Mychro.
Mychro dives deeper into an individual genome than standard pathology reports. By displaying simple genome visualisations, doctors and patients can validate their genome anomalies easier, unearth new genome insights otherwise overlooked, and begin a tailored care delivery program to better support a patient's care journey.