What happens when I go for whole genome sequencing?
Whole genome sequencing allows us look at lots of different genes with one single test. In this blog, we explain what it’s like to get whole genome sequencing, and how it may lead to a diagnosis.
Whole genome sequencing allows us look at lots of different genes with one single test. In this blog, we explain what it’s like to get whole genome sequencing, and how it may lead to a diagnosis.
This blogs talks through the role of genetic counsellors as advocates for patients, families, and the wider public, helping people to make informed decisions about genomics and their health.
A recent study found that around 14,000 patients with cancer could have reduced risk of harmful side effects from cancer treatment by receiving a lower dose or a different drug.
New research by Bradley Jermy and colleagues looks at factors affecting the accuracy of our current prediction tools, and how we could improve them.
A genetic diagnosis can impact physical health and treatment, however it can also impacts mental health and emotions. This blog revisits a podcast we recorded for Mental Health Awareness Week.
A recent study analysing genetic and clinical data from over 13,000 people with cancer has shown the benefits of using genomics in routine care.