Post by Devyser

We’re excited to be attending #ACGS2026. Join us to explore applications in rare disease and paediatric screening, including screening for conditions such as cystic fibrosis (CF) and thalassemia. Discover how advanced genomic solutions are supporting earlier detection, improving diagnostic workflows, and helping deliver better outcomes for patients and families. Looking forward to connecting with researchers, clinicians, and partners at the meeting. Andrew Wilson and Alex Clarke #RareDisease #NewbornScreening #PaediatricScreening #Genomics #CF #Thalassemia #ACGS