Blog articles

Mystery variant doubles Covid-19 severity

But how was it found, and could it help open up new avenues for treatment?

Polygenic score pilot for heart disease begins

NHS launches innovative genomic testing project that could help revolutionise heart disease identification and prevention

Diagnosing mitochondrial conditions: a WGS breakthrough

Mitochondrial conditions can be difficult to diagnose – but why, and how can genomic technology help?
Crowd of people making the shape of two kidneys viewed from above

Polycystic kidney disease and genomic testing

We explore genomics’ role in the cause, diagnosis and treatment of a complex kidney condition

GEP fellow publishes RNA splicing study

Jamie Ellingford and his co-authors explore the potential of computational tools to help us learn more about the messages our genes create

Epilepsy and the genome

We know that epilepsy can have a genetic cause, but there is still much to discover. We explore findings from two new studies to learn more

News articles

Taking action on Rare Disease Day 2022

The Genomics Education Programme releases new awareness-raising resources and supports the launch of a new action plan for rare disease in England

New educational genomics game now available

Discover an exciting card game that challenges healthcare professionals to describe genomics-related terms in jargon-free language
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A new framework for developing the workforce

A new unified approach to identify workforce development needs, aligned to patient pathways across the NHS Genomic Medicine Service, is being piloted
Groups of nurses and midwives during the working day

Genomics in Routine Care webinars now available on demand

Hear from health leaders in three webinars exploring genomics in nursing, midwifery and health visiting, now available to view online
Mother holding the hand of her newborn baby

New genomics resources for health visitors

A series of iterative documents is now available to develop health visitors’ knowledge and understanding of genomics