| Title: |
A Formative Study of the Implementation of Whole Genome Sequencing in Northern Ireland |
| Authors: |
Kerr, Katie; McKenna, Caoimhe; Heggarty, Shirley; Bailie, Caitlin; McMullan, Julie; Crowe, Ashleen; Kilner, Jill; Donnelly, Michael; Boyle, Saralynne; Rea, Gillian; Flanagan, Cheryl; McKee, Shane; McKnight, Amy Jayne |
| Source: |
Kerr, K, McKenna, C, Heggarty, S, Bailie, C, McMullan, J, Crowe, A, Kilner, J, Donnelly, M, Boyle, S, Rea, G, Flanagan, C, McKee, S & McKnight, A J 2022, 'A Formative Study of the Implementation of Whole Genome Sequencing in Northern Ireland', Genes, vol. 13, no. 7, 1104. https://doi.org/10.3390/genes13071104 |
| Publication Year: |
2022 |
| Collection: |
Queen's University Belfast: Research Portal |
| Subject Terms: |
collaboration; genomics; multiomics; public health; rare disease; /dk/atira/pure/subjectarea/asjc/1300/1311; name=Genetics; /dk/atira/pure/subjectarea/asjc/2700/2716; name=Genetics(clinical); /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being; name=SDG 3 - Good Health and Well-being |
| Description: |
Background: The UK 100,000 Genomes Project was a transformational research project which facilitated whole genome sequencing (WGS) diagnostics for rare diseases. We evaluated experiences of introducing WGS in Northern Ireland, providing recommendations for future projects. Methods: This formative evaluation included (1) an appraisal of the logistics of implementing and delivering WGS, (2) a survey of participant self-reported views and experiences, (3) semi-structured interviews with healthcare staff as key informants who were involved in the delivery of WGS and (4) a workshop discussion about interprofessional collaboration with respect to molecular diagnostics. Results: We engaged with >400 participants, with detailed reflections obtained from 74 participants including patients, caregivers, key National Health Service (NHS) informants, and researchers (patient survey n = 42; semi-structured interviews n = 19; attendees of the discussion workshop n = 13). Overarching themes included the need to improve rare disease awareness, education, and support services, as well as interprofessional collaboration being central to an effective, mainstreamed molecular diagnostic service. Conclusions: Recommendations for streamlining precision medicine for patients with rare diseases include administrative improvements (e.g., streamlining of the consent process), educational improvements (e.g., rare disease training provided from undergraduate to postgraduate education alongside genomics training for non-genetic specialists) and analytical improvements (e.g., multidisciplinary collaboration and improved computational infrastructure). |
| Document Type: |
article in journal/newspaper |
| File Description: |
application/pdf |
| Language: |
English |
| ISSN: |
2073-4425 |
| Relation: |
info:eu-repo/semantics/altIdentifier/pissn/2073-4425 |
| DOI: |
10.3390/genes13071104 |
| Availability: |
https://pure.qub.ac.uk/en/publications/0e47a0dc-2a16-4013-b2ee-8dbdec5a5a08; https://doi.org/10.3390/genes13071104; https://pureadmin.qub.ac.uk/ws/files/347192795/genes_13_01104_v3.pdf; https://www.scopus.com/pages/publications/85133007243 |
| Rights: |
info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by/4.0/ |
| Accession Number: |
edsbas.5B601AC6 |
| Database: |
BASE |