Blog articles

Whole genome sequencing for diagnosis of infants

A 2023 US study has investigated whether panel testing or whole genome sequencing is more likely to provide a molecular diagnosis, and we consider how the results apply to the NHS

What's in a little variation?

Genomic variation is the root of many of our traits, including what we look like and our susceptibility to many diseases. But what is it?
A strand of stylised blue DNA on a plain background with a magnifying glass focusing on a section of the DNA strand

How has whole genome sequencing transformed the investigation of rare disease?

The way in which rare diseases are investigated has been opened up by whole genome sequencing. We look at its impact on both clinicians and patients

First results returned from NHS cancer blood test 

Two in three patients with suspected cancer symptoms could receive an early diagnosis from a new blood test
Illustrated magnifying glass on striped background, with DNA double helices visible under the magnifying glass.

Can you spot the hidden genomics?

We've put together eight short healthcare scenarios where genomics may play a part. See if you can work it out, and click to reveal if you're right
Two illustrated health professionals in conversation

Experts through experience: Arti’s story

In today’s #GenomicsConversation blog post, we share Arti’s story of pursuing genomic testing and finding answers about her condition
Illustrated image of two health professionals in conversation

Experts through experience: Jo’s story

As part of this year’s #GenomicsConversation, patient advocate Jo shares her breast cancer journey, which began before the NHS Genomic Medicine Service was set up
Illustrated image of two health professionals in conversation

Experts through experience: Dave’s story

As part of this year’s #GenomicsConversation, we spoke to 100,000 Genomes Project participant Dave about his first-hand experiences of genomic testing in the NHS
illustrated image of two health professionals in conversation

Experts through experience: Becky’s story

Today, as part of our #GenomicsConversation week, we hear from Becky about her daughter’s complex condition, which remains undiagnosed even after genomic testing
Health professionals questioning each other

The professional view: Kate’s story

As part of #GenomicsConversation week, Professor Kate Tatton-Brown shares her personal experience of the genomic testing process and how it feels for a health professional to be a patient

News articles

GeNotes: Primary Care is now live!

The National Genomics Education programme continues to expand its flagship resource, GeNotes, with the launch of a brand-new primary care collection

Join our new solid tumour course evaluation team

Be one of the first to complete and review our new online course for clinicians unfamiliar with requesting genomic testing