Blog articles

Polygenic score pilot for heart disease begins
NHS launches innovative genomic testing project that could help revolutionise heart disease identification and prevention

Flash forward: genomics in 2022
In our second end-of-year roundup, we look ahead to three areas of genomics likely to spark discussion in the coming year

Diagnosing mitochondrial conditions: a WGS breakthrough
Mitochondrial conditions can be difficult to diagnose – but why, and how can genomic technology help?

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

New data diversity initiative launches
This week, we look at a transformative programme that aims to rapidly make genomic datasets more representative

Screening the healthy for monogenic variants
As the NHS moves towards a preventative healthcare strategy, will genomic screening for healthy people become more common?

Newborn screening: time for a genomic approach?
This week, we explore how genomics could help expand the newborn screening programme to test for many more genetic conditions

New platform to strengthen researcher-patient link
We explore how the platform will benefit its users and the steps in place to make sure it is ethical

Genomics in the NHS
This #GenomicsConversation week, we look at the genomics landscape in the UK today and the 10-year plan for the future
News articles

Master’s in Genomic Medicine: 2022/23 funding opens
The funding application process is now live for Master’s-level CPPD modules and qualifications in genomics at partner universities

Delve into whole genome sequencing
Join us this October for a deep dive into this revolutionary genomic test and learn how it is being used to benefit patients