A close-up image of a double helix

Mainstreaming whole genome sequencing: where are we now?

Genomic testing capabilities are advancing in affordability and accessibility by the day. But what is the current trajectory of whole genome sequencing in healthcare?
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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
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Hidden genomics in health visiting

In this feature article for the 2023 #GenomicsConversation week, we explore the vital role that health visitors play in unlocking the potential of genomics for patients
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
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Pharmacogenomics: The future of preventing adverse drug reactions

In the second part of our pharmacogenomics blog series, we look at how new research could lead to a more effective application of drugs

Point-of-care genomic testing suggested for stroke patients

NHS stroke patients would benefit from a one-hour genomic test, given at the point of care, to see if clopidogrel should be given, a NICE draft report suggests
A baby's fist closed around the finger of an adult.

All about mitochondria: Donation and developing treatments

In the second part of our mitochondria blog series, we look at mitochondrial donation, how it works and the impact it could have for families