Title |
Data sharing in stem cell translational science: policy statement by the International Stem Cell Forum Ethics Working Party
|
---|---|
Published in |
Regenerative Medicine, October 2015
|
DOI | 10.2217/rme.15.42 |
Pubmed ID | |
Authors |
Annelien L Bredenoord, Menno Mostert, Rosario Isasi, Bartha M Knoppers |
Abstract |
Data and sample sharing constitute a scientific and ethical imperative but need to be conducted in a responsible manner in order to protect individual interests as well as maintain public trust. In 2014, the Global Alliance for Genomics and Health (GA4GH) adopted a common Framework for Responsible Sharing of Genomic and Health-Related Data. The GA4GH Framework is applicable to data sharing in the stem cell field, however, interpretation is required so as to provide guidance for this specific context. In this paper, the International Stem Cell Forum Ethics Working Party discusses those principles that are specific to translational stem cell science, including engagement, data quality and safety, privacy, security and confidentiality, risk-benefit analysis and sustainability. |
X Demographics
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United States | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Practitioners (doctors, other healthcare professionals) | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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United States | 1 | 2% |
Unknown | 44 | 98% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Ph. D. Student | 9 | 20% |
Researcher | 8 | 18% |
Unspecified | 6 | 13% |
Student > Bachelor | 3 | 7% |
Professor | 2 | 4% |
Other | 6 | 13% |
Unknown | 11 | 24% |
Readers by discipline | Count | As % |
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Medicine and Dentistry | 7 | 16% |
Unspecified | 6 | 13% |
Computer Science | 3 | 7% |
Social Sciences | 3 | 7% |
Nursing and Health Professions | 2 | 4% |
Other | 13 | 29% |
Unknown | 11 | 24% |