Utilizing artificial intelligence & whole genome analysis to increase patient outcomes and lower direct costs
We offer the world’s most complete genomic analysis
At Frelii we do a full genome sequencing of 3.2 Billion individual data points. After sequencing, we run the data through our patented artificial intelligence “Navi”. Navi’s complete analysis includes analyzing every data point against all existing published genomic studies, as well as analyzing every data point against all other data points. (This process takes more than 7,680,000,000 gigs of computational processing per individual) This gives us the most comprehensive genetic results on the planet and helps us give real answers to potential patient needs or risks.
Learn more about us and our process
InvestorsWe are transparent with all our current and potential investors. See all Frelii related news, press releases and our public and corporate filings here.
If you’ve got questions then we have the answers. In order to save time here’s a list of the most frequent questions we get asked.
Want to know the story behind Frelii’s world changing technology? Meet the teams of scientists, tech professionals and business leaders who came together to make it happen.