Unique are calling for clinicians to lead development of five to ten new Unique Information Guides for rare genetic neurodevelopmental disorders using a customised AI solution developed as part of a collaborative project between Unique, Manchester Rare Conditions Centre, Shorthills AI and NW GMSA.
Unique produces condition-specific information guides written in accessible language. We currently have over 300 condition-specific guides and 550 translations, in our freely available online guide library. However, with the ever-increasing provision of diagnoses and limited resources, generating new guides, and updating older guides, is a major challenge. The new AI model can shorten the time needed for developing new guides.
Get involved in this exciting project, submit your proposal – https://forms.office.com/e/jziupyz04f – by 30ᵗʰ May and impact lives across the world!
