The Ethics of Consent in a Shifting Genomic Ecosystem.

IF 7 Q1 MATHEMATICAL & COMPUTATIONAL BIOLOGY Annual Review of Biomedical Data Science Pub Date : 2021-07-20 DOI:10.1146/annurev-biodatasci-030221-125715
Sandra Soo-Jin Lee
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引用次数: 6

Abstract

The collection and use of human genetic data raise important ethical questions about how to balance individual autonomy and privacy with the potential for public good. The proliferation of local, national, and international efforts to collect genetic data and create linkages to support large-scale initiatives in precision medicine and the learning health system creates new demands for broad data sharing that involve managing competing interests and careful consideration of what constitutes appropriate ethical trade-offs. This review describes these emerging ethical issues with a focus on approaches to consent and issues related to justice in the shifting genomic research ecosystem.

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在不断变化的基因组生态系统中的同意伦理。
人类基因数据的收集和使用引发了重要的伦理问题,即如何在个人自主权和隐私与潜在的公共利益之间取得平衡。地方、国家和国际上收集遗传数据和建立联系以支持精准医学和学习型卫生系统的大规模倡议的努力的扩散,对广泛的数据共享产生了新的需求,这涉及管理相互竞争的利益和仔细考虑什么构成适当的伦理权衡。这篇综述描述了这些新兴的伦理问题,重点是在不断变化的基因组研究生态系统中,同意的方法和与正义相关的问题。
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来源期刊
CiteScore
11.10
自引率
1.70%
发文量
0
期刊介绍: The Annual Review of Biomedical Data Science provides comprehensive expert reviews in biomedical data science, focusing on advanced methods to store, retrieve, analyze, and organize biomedical data and knowledge. The scope of the journal encompasses informatics, computational, artificial intelligence (AI), and statistical approaches to biomedical data, including the sub-fields of bioinformatics, computational biology, biomedical informatics, clinical and clinical research informatics, biostatistics, and imaging informatics. The mission of the journal is to identify both emerging and established areas of biomedical data science, and the leaders in these fields.
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