RareOmics has been archived

RareOmics was a free service that Healx built to help members of the rare disease community build a news feed of the latest research around their disease of interest. It used our natural language processing to find mentions of rare diseases in journal articles and build a news feed to the latest and most popular research.

We’re very grateful to everyone who previously signed up and used RareOmics in the years it was running. If you would like an alternative way to track rare disease research you could try signing up for PubMed alerts.