The human genome is made up of 3 billion letters of DNA (A, T, C and G). Whole genome sequencing is a technique that is used to ‘read’ these letters and finds their order one by one. The digital ...

NHS patients will be told their real-time cancer risk with the help of smartwatches and other gadgets. Everyone will be able ...

Humber Teaching NHS FT has enabled its EPR move to the cloud through Dedalus’ Healthcare Platform. With the trust’s strategy being to move core applications to the cloud, the platform has provided a ...

The three-year study – led by mental health data science company Akrivia Health in partnership with Cardiff University – will create "the most detailed dataset ever" on serious mental health ...

Safi was born at the Rosie Hospital, Cambridge in December 2024. She was one of the first babies participating in the Generation Study that went on to be diagnosed with a rare genetic condition.

Ana Lisa Tavares, Clinical Lead for Rare Disease Research at Genomics England, shares her thoughts on the 'hype and hope' ...

Job Description Key responsibilities Working collaboratively with the Participant Panel Chair and Vice-Chair for Rare Conditions: Help to shape ...

On 4, PharosAI announced it would use 10x Genomics’ Xenium spatial platform to convert archived NHS cancer samples into high-resolution, multimodal datasets, backed by £18.9 million in UK government ...

Mark Stephenson, CEO, Reframe Cancer, discusses the National Cancer Plan and how the private market fits into the nation’s Cancer care strategy.