Blog articles

Four types of genomic testing explained

In the age of genomics, it can be difficult to understand the ins and outs of different types of testing; here we break down four of the most common 

Patient perspectives: the art of good communication

In the second article covering our recent patient panel event, we consider the issue that both panellists and audience members agreed was most important

Patient perspectives: managing expectations

Following our insightful patient panel event on 6th March, we explore the importance of preparing for the highs, and lows, of genomic testing

Hereditary haemochromatosis a 'stealth disease’

Recent genomic research has shed new light on the condition, previously thought to be low risk, prompting a review of screening regulation 

Counselling the code: genomic testing and insurance

Genetic counsellor Megan Rogers looks at the new Code on Genetic Testing and Insurance and what it means for patients and counsellors

All I want for Christmas is... a family history

At a time of year when many of us will be getting together with relatives, we explore the value of talking about your family's health

News articles

New guide for clinicians feeding back genomic results

Clinicians returning rare disease results to 100,000 Genomes Project participants can use this handy 2-page guide, with further resources to follow

Competency framework for consent: reviewers sought

We are inviting feedback on a new competency framework that outlines the key elements required for clinicians to seek consent for a genomic test

Additional 'Genomics in Medical Specialties' films launched

Three additional films and supporting information illustrate the ways in which genomics is changing clinical practice across the NHS

Review our guide to returning genomic test results

We have developed a short guide for clinicians returning participant results from the 100,000 Genomes Project - and we'd like your feedback