This November is set to be a busy one, with Genomics Cafés taking place in person across Wales.
Our programme of in-person cafés kicks off at Xplore! Science Discovery Centre in Wrexham on Thursday, 13 November, where the talks will focus on a range of patient organisations.
The session features the following talks:
Optimising Rare Disease Healthcare and Family Support; A Case Study – Jayne Hughes, CEO Amy and Friends
Update on the new Genomics Delivery Plan for Wales – Genomics Partnership Wales
Unique experiences: living with a rare chromosome or gene disorder – UNIQUE
We then move across the country to the Institute of Life Science at Swansea University, where on Wednesday, 19 November, we will explore a range of genomics research taking place at the university and beyond as well as hearing from patient organisations.
The session features the following talks:
New Methods to Diagnose Rare Diseases: A Project Update – Professor William Griffiths, Swansea University
Challenges and opportunities in rare disease research – Laura Morris & Imogen Bennett, Swansea University
Exploring precision medicine and early detection of cancer with linked genomic and population health records – Dr Arron Lacey, Lecturer in Health Data Science at SAIL Databank, Swansea University
Popham Kidney Support
Both sessions are a great opportunity to learn more about the range of genomics and genetics work happening in and around Wales. To book either of the events, follow this link – https://www.ticketsource.co.uk/wales-gene-park.
We look forward to seeing you in person for some exciting talks!
P.S. If you can’t make either of these sessions, keep your eyes peeled for a special festive café being announced in the coming weeks!