Genomics England PanelApp
The 100 000 Genomes Project: bringing whole genome sequencing to the NHS | The BMJ
Advances in Rare Disease Diagnosis | PhenoTips
PDF) Summary Document - NHS Genomic Medicine Centres: National Service Evaluation of the Consent Process and Participant Materials used in the 100,000 Genomes Project
300+ 份“Ellen Thomas”的职业档案| 领英
The contribution of common regulatory and protein-coding TYR variants in the genetic architecture of albinism | medRxiv
PDF) Clinical Analysis of Whole Genome Sequencing in Cancer Patients
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis | Genetics in Medicine
The Role of Genomics in Mainstream Medicine - M4RD
PDF) Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study
Twitter takover – Dr Ellen Thomas / Twitter
Emma Baple and Dom McMullan 20th February ppt download
The Role of Genomics in Mainstream Medicine - M4RD
300+ "Ellen Thomas" profiles | LinkedIn
300+ "Ellen Thomas" profiles | LinkedIn
The Role of Genomics in Mainstream Medicine - M4RD
Genomics England Innovation Showcase 21
Genomics England update - ppt download
Genomics England PanelApp
The G Word on Apple Podcasts
Genomics England PanelApp
Richard Scott - Chief Medical Officer - Genomics England | LinkedIn
Evaluating the performance of a clinical genome sequencing program for diagnosis of rare genetic disease, seen through the lens of craniosynostosis | Genetics in Medicine
Ellen Thomas's research works | Queen Mary, University of London, London (QMUL) and other places
Low grade mosaicism in hereditary haemorrhagic telangiectasia identified by bidirectional whole genome sequencing reads through the 100,000 Genomes Project clinical diagnostic pipeline | Journal of Medical Genetics
