The goal of this call is to support hypotheses driven research projects aiming at exploring genetic and molecular bases of rare diseases by the use of NGS approaches (WES, WGS, RNA–seq, small RNA–seq, ChIP–seq, Methyl–seq, etc.)
Priority will be given to projects that:
– focus on well–characterized clinical phenotypes for which a genetic basis is postulated but not fully demonstrated,
– that show potential leading to molecular diagnosis or therapeutic approaches in clinics,
– for which applicants can demonstrate the availability of expert bioinformatics hub.
Projects based on exome sequencing of modifying genes are henceforth considered outside
the scope of this call.
This program is open to research projects covering all rare diseases.
Submission deadline January 19, 2023, 5:00 pm (CET)