Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
6th Plenary – GA4GH
PanelApp Australia
G2P: Using machine learning to understand and predict genes causing rare neurological disorders | bioRxiv
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
6th Plenary – GA4GH
Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study - The Lancet Neurology
Genomics England PanelApp
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report | NEJM
PDF) 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report | tanya lam - Academia.edu
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report | NEJM
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
Eleanor Williams (@williams_e_m) / X
People - Open Targets
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study - The Lancet Neurology
Ellen McDonagh, Open Targets Informatics Sci Director | People | EMBL's European Bionformatics Institute