Participant Experiences of the 100,000 Genomes Project
18 July 2019
Participant Experiences of the 100,000 Genomes Project
As a member of Genetic Alliance, Nerve Tumours UK welcomes their latest research and survey results
Genomics England commissioned Genetic Alliance UK to seek the views of patients and carers around the introduction of Whole Genome Sequencing into the NHS. They also wanted to hear about people’s experiences of taking part in the 100,000 Genomes Project ( A project that sequenced 100,000 genomes from around 85,000 people. Participants were NHS patients with a rare disease, plus their families, and patients with cancer).
Here are some of the key findings:
1. The majority of our respondents were glad they had taken part in the 100,000 Genomes Project:
(73%), would take part again (86%), and would be likely to participate in future medical and genomic research.
2. However, fewer than half (43%) of our respondents said they were ‘satisfied’ or ‘very satisfied’ with their overall experience of taking part in the 100,000 Genomes Project. Respondents indicated that the benefits they hoped for from taking part were not matched by actual benefits achieved at the time of the survey.
3. Most respondents (77%) had yet to receive a result at the time of our survey, which offers a likely explanation for the discrepancy between findings 1 and 2.
4. Over 80% of patients and carers felt they had been provided with sufficient, comprehensible information about the 100,000 Genomes Project before taking part. However they would have liked more information about what to expect during the process, and more regular contact while waiting for a result.
If you would like to find out about the full results of the study you can do so by clicking on the link below:
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Embracing-complexityPage-Preview-800-x-500-px_800_600_s_c1.png)
Nerve Tumours UK joins the “Embracing Complexity” Coalition
Find out more about the coalition we have decided to join
Read More![](https://nervetumours.org.uk/images/made/images/common/UON-2Artboard-1_800_600_s_c1.png)
Researching NF1
Rory Deasy has conducted research into the treatment of children with NF1. Here he talks about his research journey.
Read More![](https://nervetumours.org.uk/images/made/images/common/MeganPage-Preview-800-x-500-px_800_600_s_c1.png)
Megan’s Journey
Megan talks about her experiences of being a student with NF and what she took away from the NF conference in San Fransico
Read More![](https://nervetumours.org.uk/images/made/images/common/Aldo-Goes-to-Primary-SchoolPage-Preview-800-x-500-px_800_600_s_c1.png)
Aldo goes to Primary School
Find out more about the book aimed at helping people understand the life of an autistic boy going through primary school here
Read More![](https://nervetumours.org.uk/images/made/images/common/Eva-Page-Preview-800-x-500-px_800_600_s_c1.png)
Eva’s Races
Eva has run 3 races over the past year for NTUK, find out what has been motivating her here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Carls-story-Page-Preview-800-x-500-px_800_600_s_c1.png)
Carl’s Story in memory of his sister who had NF2
Carl recently hosted his own wrestling event in memory of his late sister, find out more on his story here:
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK-dolphinsPage-Preview-800-x-500-px_800_600_s_c1.png)
NTUK Dolphins at the Swim Serpentine 2019
Find out more about the incredible day for all involved at Hyde Park here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Rotary-JazzPage-Preview-800-x-500-px_800_600_s_c1.png)
Rotary’s Summer Evening Jazz Concert in aid of NTUK
Find out more about the amazing Jazz Concert that was hosted in aid of NTUK here:
Read More![](https://nervetumours.org.uk/images/made/images/common/Wrestling-done-1Page-Preview-800-x-500-px_800_600_s_c1.png)
K-Star Wrestling in aid of NTUK
Find out more about the successful wrestling event that took place in aid of NTUK
Read More