A human rights approach to an international code of conduct for genomic and clinical data sharing

Fostering data sharing is a scientific and ethical imperative. Health gains can be achieved more comprehensively and quickly by combining large, information-rich datasets from across conventionally siloed disciplines and geographic areas. While collaboration for data sharing is increasingly embraced...

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Detalles Bibliográficos
Autores principales: Knoppers, Bartha M., Harris, Jennifer R., Budin-Ljøsne, Isabelle, Dove, Edward S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053599/
https://www.ncbi.nlm.nih.gov/pubmed/24573176
http://dx.doi.org/10.1007/s00439-014-1432-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4053599/
https://www.ncbi.nlm.nih.gov/pubmed/24573176
http://dx.doi.org/10.1007/s00439-014-1432-6

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