Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial

INTRODUCTION: Genome sequencing, a novel genetic diagnostic technology that analyses the billions of base pairs of DNA, promises to optimise healthcare through personalised diagnosis and treatment. However, implementation of genome sequencing faces challenges including the lack of consensus on discl...

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Detalles Bibliográficos
Autores principales: Shickh, Salma, Clausen, Marc, Mighton, Chloe, Casalino, Selina, Joshi, Esha, Glogowski, Emily, Schrader, Kasmintan A, Scheer, Adena, Elser, Christine, Panchal, Seema, Eisen, Andrea, Graham, Tracy, Aronson, Melyssa, Semotiuk, Kara M, Winter-Paquette, Laura, Evans, Michael, Lerner-Ellis, Jordan, Carroll, June C, Hamilton, Jada G, Offit, Kenneth, Robson, Mark, Thorpe, Kevin E, Laupacis, Andreas, Bombard, Yvonne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Genetics and Genomics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5922516/
https://www.ncbi.nlm.nih.gov/pubmed/29700101
http://dx.doi.org/10.1136/bmjopen-2018-021876

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5922516/
https://www.ncbi.nlm.nih.gov/pubmed/29700101
http://dx.doi.org/10.1136/bmjopen-2018-021876

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