The Rare Diseases Foundation is pleased to announce the launch of its call for research projects 'GenOmics: high throughput sequencing & rare diseases'.
The objective of this call for projects is to support research projects aiming at elucidating the genetic and molecular basis of rare diseases by relying on high throughput sequencing.
The support of the Rare Diseases Foundation will allow project leaders to access the most innovative high-throughput sequencing technologies for the analysis of the exome, genome, transcriptome and epigenome.
Please find attached the text of the call for projects.
The deadline for submission of projects is *Thursday, September 24, 2020, 5:00 pm*.