Openness in Big Data and Data RepositoriesThe Application of an Ethics Framework for Big Data in Health and Research

被引:0
作者
Vicki Xafis
Markus K. Labude
机构
[1] Yong Loo Lin School of Medicine,Centre for Biomedical Ethics
来源
Asian Bioethics Review | 2019年 / 11卷
关键词
Big data; Open data; Open science; Data repository; Decision-making framework; Health data;
D O I
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中图分类号
学科分类号
摘要
There is a growing expectation, or even requirement, for researchers to deposit a variety of research data in data repositories as a condition of funding or publication. This expectation recognizes the enormous benefits of data collected and created for research purposes being made available for secondary uses, as open science gains increasing support. This is particularly so in the context of big data, especially where health data is involved. There are, however, also challenges relating to the collection, storage, and re-use of research data. This paper gives a brief overview of the landscape of data sharing via data repositories and discusses some of the key ethical issues raised by the sharing of health-related research data, including expectations of privacy and confidentiality, the transparency of repository governance structures, access restrictions, as well as data ownership and the fair attribution of credit. To consider these issues and the values that are pertinent, the paper applies the deliberative balancing approach articulated in the Ethics Framework for Big Data in Health and Research (Xafis et al. 2019) to the domain of Openness in Big Data and Data Repositories. Please refer to that article for more information on how this framework is to be used, including a full explanation of the key values involved and the balancing approach used in the case study at the end.
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页码:255 / 273
页数:18
相关论文
共 65 条
[1]  
Erlich Yaniv(2018)Identity inference of genomic data using long-range familial searches Science 362 690-694
[2]  
Shor Tal(2018)Data sharing in PLOS ONE: an analysis of Data Availability Statements PLoS One 13 e0194768-25
[3]  
Pe’er Itsik(2011)Assessing the privacy risks of data sharing in genomics Public Health Genomics 14 17-228
[4]  
Carmi Shai(2016)Comparing the overall result and interaction in aggregate data meta-analysis and individual patient data meta-analysis Medicine 95 e3312-277
[5]  
Federer LM(2005)Contradicted and initially stronger effects in highly cited clinical Research JAMA 294 218-67
[6]  
Belter CW(2016)Data sharing New England Journal of Medicine 374 276-1425
[7]  
Joubert DJ(2013)Open access digital data sharing: principles, policies and practices Social Epistemology 27 47-1777
[8]  
Livinski A(2015)Scientific standards. Promoting an open research culture Science 348 1422-386
[9]  
Lu Y-L(2010)Broken promises of privacy: responding to the surprising failure of anonymization UCLA Law Review 57 1701-6
[10]  
Snyders LN(2016)Sharing clinical trial data—a proposal from the International Committee of Medical Journal Editors New England Journal of Medicine 374 384-24