Research is personal. Tomorrow’s episode features Carlos Guerrero & Angie Weaver from Chan Zuckerberg Initiative #RareAsOne Project, sharing what it’s really like to live in the world of rare disease—where research can mean everything.
#PatientStories #ResearchMatters #RareDiseaseCommunity

Advancing Science to Build a World without NEC The NEC Biorepository, led by Dr. Misty Good, is advancing research to improve our ability to understand, diagnose, prevent, and treat necrotizing enterocolitis.…

Check out how the NEC Biorepository, led by @mistygoodlab.bsky.social, is advancing research to improve our ability to understand, diagnose, prevent, and treat necrotizing enterocolitis.

#preventNEC #RareAsOne

vimeo.com/1027372472

GeniE, the Genetic Prevalence Estimator | gnomAD browser The Genome Aggregation Database (gnomAD) is a resource developed by an international coalition of investigators, with the goal of aggregating and harmonizing both exome and genome sequencing data from...

Thank you to everyone who contributed to this project (broad.io/genie_blog_a...), but especially our co-developers Chan Zuckerberg Initiative's #RareAsOne Network. This tool was inspired by the rare disease advocacy community and I am so grateful to count you all as collaborators (3/4)