The Rare Diseases Foundation launches its new call for projects "GenOmics: high throughput sequencing" and supports a key step in understanding the genetic causes of rare diseases.
The Rare Diseases Foundation supports French research teams by facilitating their access to the most innovative high-throughput sequencing technologies. This call for projects aims to support research projects aimed at elucidating the genetic and molecular basis of rare diseases and is in line with the Foundation's desire to accelerate the diagnosis of rare diseases.
Click here for the text of this call for projects.
