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
![Become a Trustee](https://nervetumours.org.uk/images/made/images/templates/placeholder_800_600_s_c1.png)
Become a Trustee
Nerve Tumours UK are looking for at least two new trustees to join the Board. Find out more
Read More![](https://nervetumours.org.uk/images/made/images/common/Guys_and_St_Thomas_Foundation_Trust_logo_370x280_800_600_s_c1.jpg)
Guy’s Hospital NF Centre Coffee Meetings
Guy's Hospital Neurofibromatosis Centre Coffee Club 2024
Read More![](https://nervetumours.org.uk/images/made/images/common/Liz_Barton_370x280_800_600_s_c1.jpg)
Liz’s NF1 story: This is the real me
Liz describes growing up with NF1, difficulties at school, spinal surgery and raising awareness by writing a poem about NF.
Read More![](https://nervetumours.org.uk/images/made/images/common/Contact_logo_for_joint_work_Pears_370x280_800_600_s_c1.jpg)
Stronger Together Rare Conference
Read this review of the conference and find out where to access further support
Read More![](https://nervetumours.org.uk/images/made/images/common/Gisela_wearing_NTUK_Tshirt_370x280_800_600_s_c1.jpg)
Gisela’s NF2 story
Gisela has NF2 & has a positive outlook on life, she has just completed a 265km walk during World NF Awareness Month
Read More![](https://nervetumours.org.uk/images/made/images/common/image002_(1)_370x280_800_600_s_c1.jpg)
Oxford’s John Radcliffe Hospital celebrate NF2 Awareness Day
We set out to promote and educate people about NF2 & the service offered in Oxford & Southwest Region for patients
Read More![](https://nervetumours.org.uk/images/made/images/common/2560px-Care_Quality_Commission_logo_370x280_800_600_s_c1.jpg)
Care Quality Commission survey
Take part - if you are from an ethnic minority, have a long term physical condition & live in selected SW London boroughs
Read More![](https://nervetumours.org.uk/images/made/images/common/Recruit_advert_Family_Planning_and_decision_making_370x280_800_600_s_c1.jpg)
CAR research family planning decision making
This CAR UWE research explores family planning & decision making for people with a visible difference which can be inherited
Read More