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PanelApp crowdsources expert knowledge to establish consensus diagnostic  gene panels | Nature Genetics
PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels | Nature Genetics

G2P: Using machine learning to understand and predict genes causing rare  neurological disorders | bioRxiv
G2P: Using machine learning to understand and predict genes causing rare neurological disorders | bioRxiv

Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University,  CA | SU | Queen Mary University of London
Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University, CA | SU | Queen Mary University of London

PanelApp (@PanelAppTeam) / Twitter
PanelApp (@PanelAppTeam) / Twitter

PanelApp (@PanelAppTeam) / Twitter
PanelApp (@PanelAppTeam) / Twitter

PanelApp crowdsources expert knowledge to establish consensus diagnostic  gene panels | Nature Genetics
PanelApp crowdsources expert knowledge to establish consensus diagnostic gene panels | Nature Genetics

Welcome: Ellie McDonagh | EMBL
Welcome: Ellie McDonagh | EMBL

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS |  The BMJ
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS | The BMJ

Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University,  CA | SU | Queen Mary University of London
Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University, CA | SU | Queen Mary University of London

Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University,  CA | SU | Queen Mary University of London
Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University, CA | SU | Queen Mary University of London

Australian Genomics launches local instance of… | Genomics England
Australian Genomics launches local instance of… | Genomics England

Scaling national and international improvement in virtual gene panel  curation via a collaborative approach to discordance resolution -  ScienceDirect
Scaling national and international improvement in virtual gene panel curation via a collaborative approach to discordance resolution - ScienceDirect

Genomics England on Twitter: "Happy 5th birthday @PanelAppTeam! We are very  proud of all that has been achieved - none of which would be possible  without the support and contributions from curators,
Genomics England on Twitter: "Happy 5th birthday @PanelAppTeam! We are very proud of all that has been achieved - none of which would be possible without the support and contributions from curators,

The 100 000 Genomes Project: bringing whole genome sequencing to the NHS |  The BMJ
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS | The BMJ

Ellen Thomas « 2022 ESDR Annual Meeting
Ellen Thomas « 2022 ESDR Annual Meeting

PanelApp Australia
PanelApp Australia

Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University,  CA | SU | Queen Mary University of London
Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University, CA | SU | Queen Mary University of London

G2P: Using machine learning to understand and predict genes causing rare  neurological disorders | bioRxiv
G2P: Using machine learning to understand and predict genes causing rare neurological disorders | bioRxiv

PanelApp (@PanelAppTeam) / Twitter
PanelApp (@PanelAppTeam) / Twitter

Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University,  CA | SU | Queen Mary University of London
Ellen MCDONAGH | Lead Scientific Curator | Bsc, PhD. | Stanford University, CA | SU | Queen Mary University of London

PDF) 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care —  Preliminary Report | Angela Douglas - Academia.edu
PDF) 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report | Angela Douglas - Academia.edu

Genomics England Archives - Global Genes
Genomics England Archives - Global Genes

Single‐base substitutions in the CHM promoter as a cause of choroideremia -  Radziwon - 2017 - Human Mutation - Wiley Online Library
Single‐base substitutions in the CHM promoter as a cause of choroideremia - Radziwon - 2017 - Human Mutation - Wiley Online Library

Genomics England PanelApp
Genomics England PanelApp

Genomics England PanelApp
Genomics England PanelApp

Open Targets - #OpenTargetsNews We have a new Informatics Science Director, Ellen  McDonagh! 🎉🎊 Ellen has has joined the European Bioinformatics Institute  (EMBL-EBI) and will oversee and further develop our informatics research
Open Targets - #OpenTargetsNews We have a new Informatics Science Director, Ellen McDonagh! 🎉🎊 Ellen has has joined the European Bioinformatics Institute (EMBL-EBI) and will oversee and further develop our informatics research

Single‐base substitutions in the CHM promoter as a cause of choroideremia -  Radziwon - 2017 - Human Mutation - Wiley Online Library
Single‐base substitutions in the CHM promoter as a cause of choroideremia - Radziwon - 2017 - Human Mutation - Wiley Online Library