Cargando…
Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study
With large-scale genome sequencing initiatives underway, vast amounts of genomic data are being generated. Results—including secondary findings (SF)—are being returned, although policies around generation and management remain inconsistent. In order to inform relevant policy, it is essential that th...
Autores principales: | Mackley, Michael P, Blair, Edward, Parker, Michael, Taylor, Jenny C, Watkins, Hugh, Ormondroyd, Elizabeth |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945590/ https://www.ncbi.nlm.nih.gov/pubmed/29440777 http://dx.doi.org/10.1038/s41431-018-0106-6 |
Ejemplares similares
-
Stakeholder views on secondary findings in whole-genome and whole-exome
sequencing: a systematic review of quantitative and qualitative studies
por: Mackley, Michael P., et al.
Publicado: (2017) -
“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project
por: Ormondroyd, Elizabeth, et al.
Publicado: (2017) -
Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study
por: Ormondroyd, Elizabeth, et al.
Publicado: (2017) -
Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes
por: Ormondroyd, Elizabeth, et al.
Publicado: (2020) -
Genomic health data generation in the UK: a 360 view
por: Ormondroyd, Elizabeth, et al.
Publicado: (2021)