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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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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4053599/ https://ncbi.nlm.nih.gov/pubmed/24573176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-014-1432-6 |
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