Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing

W Steyaert, L Sagath, G Demidov, VA Yepez… - medRxiv, 2024 - medrxiv.org
Solve-RD is a pan-European rare disease (RD) research program that aims to identify
disease-causing genetic variants in previously undiagnosed RD families. We utilized 10-fold …

Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing

W Steyaert, L Sagath, G Demidov, VA Yépez… - medRxiv - ncbi.nlm.nih.gov
Solve-RD is a pan-European rare disease (RD) research program that aims to identify
disease-causing genetic variants in previously undiagnosed RD families. We utilised 10-fold …

Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing.

W Steyaert, L Sagath, G Demidov… - Medrxiv: the Preprint …, 2024 - europepmc.org
Solve-RD is a pan-European rare disease (RD) research program that aims to identify
disease-causing genetic variants in previously undiagnosed RD families. We utilised 10-fold …

Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing

W Steyaert, L Sagath, G Demidov… - … : the preprint server …, 2024 - pubmed.ncbi.nlm.nih.gov
Solve-RD is a pan-European rare disease (RD) research program that aims to identify
disease-causing genetic variants in previously undiagnosed RD families. We utilised 10-fold …

Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing

W Steyaert, L Sagath, G Demidov, VA Yépez… - 2024 - europepmc.org
Solve-RD is a pan-European rare disease (RD) research program that aims to identify
disease-causing genetic variants in previously undiagnosed RD families. We utilised 10-fold …