Clinical Genomics: Fundamentals of Variant Interpretation in Clinical Practice
Wellcome Genome Campus, Hinxton, CB10 1RQ, UK
This re-vamped course, previously called Fundamentals of Clinical Genomics, will address the scientific aspects of human genetics and genomics that underpin genetic diagnostics and clinical practice, focusing on the latest technological and bioinformatics developments to enable better interpretation of genetic variants.
This advanced course is suitable for both clinical geneticists (consultants and trainees) and clinical scientists delivering genetic healthcare, and is designed to equip attendees with the skills required to work in the fast-paced, new era of genomic medicine. Applications from other clinicians who are using genomic data in their everyday practice are also welcome.
The course will be delivered by leaders in genomics and participants will have the opportunity to learn from those who developed the tools and are working at the cutting edge of genomic medicine.
Wellcome Genome Campus – Advanced Courses and Scientific Conferences
Diana Baralle – University of Southampton, UK
Sian Ellard – University of Exeter, UK
David FitzPatrick – University of Edinburgh, UK
Julia Foreman – Wellcome Sanger Institute, UK
Matt Hurles – Wellcome Sanger Institute, UK
Serena Nik Zainal – University of Cambridge, UK
Andrew Read – University of Manchester, UK
Kaitlin Samocha – Wellcome Sanger Institute, UK
Richard Scott – Genomics England, UK
Patrick Tarpey – Cambridge University Hospitals, UK
Kate Thomson – Oxford University Hospitals, UK
Marc Tischkowitz – University of Cambridge, UK
Clare Turnbull – The Institute of Cancer Research, UK
Clara van Karnebeek – University of Amsterdam, The Netherlands
James Ware – Imperial College London, UK
Nicola Whiffin – Imperial College London, UK
Andrew Wilkie – University of Oxford, UK