Genomics England PanelApp
People - Open Targets
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
Genomics England PanelApp
PanelApp Australia
G2P: Using machine learning to understand and predict genes causing rare neurological disorders | bioRxiv
People - Open Targets
6th Plenary – GA4GH
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
6th Plenary – GA4GH
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report | NEJM
Genomics England PanelApp
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
G2P: Using machine learning to understand and predict genes causing rare neurological disorders | bioRxiv
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
Eleanor Williams (@williams_e_m) / X
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
PanelApp Australia
Ellen McDonagh - Translational Informatics Director - Open Targets | LinkedIn
Kristina IBÁÑEZ | Senior data scientist in genomics | PhD | Queen Mary, University of London, London | QMUL | Research profile
Genomics England PanelApp
Volume 51 Issue 11, November 2019
Arianna TUCCI | Clinical Geneticist MD PhD | MD, PhD | 100000 Genomes Project | Research profile
People - Open Targets
A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage | Nature Cancer
