Blog articles
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
Why mRNA vaccines aren't gene therapies
We bust another Covid-19 myth – this time about how mRNA vaccines work – in our latest blog post
Global genomes sequenced in new study
Genomic datasets are widely used by researchers, but are they representative enough? We look at recent research that aims to shift the balance
News articles
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