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UK launches new rare diseases strategy

The UK has launched a new framework which aims to raise awareness of rare diseases, speed up diagnosis and improve […]

All Wales, All the way!

Megan Fealey, NovaSeq Implementation Lead, and Joseph Halstead, Bioinformatician, from All Wales Medical Genomics Service (AWMGS) joined us to discuss […]

Women in genetics

Can you name a female scientist? For many people reading this, this may seem like a very easy question to […]

Günther Brueggenwerth and Arndt Schmitz from Bayer tell us about Radiomics

We caught up with Günther Brueggenwerth and Arndt Schmitz from Bayer at the Festival of Genomics in January to talk […]

The UK is developing a new approach to patient-centric precision medicine research

Sano Genetics, Zetta Genomics and Genomics England have partnered to develop a novel system to allow rare disease patients and […]

Interview with Derek Burke, Regional Manager at WekaIO

Derek Burke has sixteen years’ experience in scale-out computing, introducing new technologies across Europe. He has previously held the VP […]

Interview with Jeanette Mostert, Radboud University Medical Center

Jeanette Mostert (PhD) is science dissemination manager at the department of genetics of the Radboud University Hospital Medical Center in […]

Interview with Seven Bridges: Bill Moss, CEO and Brandi Davis- Dusenbery, CSO tell us what the future holds for Big Data

Data is more than just a hot topic; everyone is focusing on how they can better gather, handle and manipulate […]

Interview with Dr Luigi Grassi, Informatics Scientist, AstraZeneca

I’m Luigi Grassi and I’m an Informatics Scientist at AstraZeneca. I’m responsible for designing and performing bioinformatical analyses of the […]

Providing Information And Support to Families Affected by Rare Genetic Diseases – Interview with Arti Patel, Unique

Arti Patel is an Information Officer at Unique, where she acts as the first point of contact on the helpline […]