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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...
Uloženo v:
| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Berlin Heidelberg
2014
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| Témata: | |
| On-line přístup: | 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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