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
South West Genomic Laboratory Hub (@SWGLH) | Nitter | PussTheCat.org
Emma Baple and Dom McMullan 20th February ppt download
Advances in Rare Disease Diagnosis | PhenoTips
Ellen Thomas's research works | Queen Mary, University of London, London (QMUL) and other places
The G Word on Apple Podcasts
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 G Word | Podcasts on Audible | Audible.com
PDF) Summary Document - NHS Genomic Medicine Centres: National Service Evaluation of the Consent Process and Participant Materials used in the 100,000 Genomes Project
Genomics England update - ppt download
Genomics England PanelApp
Genomics England on Twitter: "Our #GenomicMedicineService in the @NHS session with @chris_wigley, @CSOSue and Dr Ellen Thomas is starting at 10.45 - don't miss out! @genomicsedu @NorthThamesGLH @SWGLH @NEYGenomics @NHSgms Register here
Twitter takover – Dr Ellen Thomas / Twitter
Richard Scott - Chief Medical Officer - Genomics England | LinkedIn
Genomics England update - ppt download
Ellen Thomas « 2022 ESDR Annual Meeting
300+ "Ellen Thomas" profiles | LinkedIn
PDF) Clinical Analysis of Whole Genome Sequencing in Cancer Patients
Whole genome sequencing increases diagnosis of rare disorders by nearly a third | University of Cambridge
The Role of Genomics in Mainstream Medicine - M4RD
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
Twitter takover – Dr Ellen Thomas / Twitter
300+ "Ellen Thomas" profiles | LinkedIn
PanelApp Australia
