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Informed Consent in Forensic DNA Databases: Volunteering, Constructions of Risk and Identity Categorization

机译:法医DNA数据库中的知情同意:志愿服务,风险构建和身份分类

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摘要

In this article we aim to expand the traditional ethical issues related to the use and storage of genetic information in forensic DNA databases by exploring the Portuguese practices of informed consent in the context of DNA sample collection for forensic processing. This article focuses on three interrelated domains: the practice of volunteering to contribute to the Portuguese forensic DNA database; the portfolio of risks presented to DNA donors; and the ethical implications of requesting donors' ethnic group among their personal data. We argue that the Portuguese forensic DNA database is an interesting case study to re-focus the ethical debate on the implications of collecting genetic information, elucidating how this activity reconfigures interpersonal relations and social hierarchy, the power of legal medicine and criminal justice, and the social construction of personal autonomy, privacy and individual rights. The practices of informed consent need to incorporate answers to risks and uncertainties posed by collecting DNA samples and DNA profiling in forensic genetic databases.
机译:在本文中,我们旨在通过探讨在法医处理DNA样本收集的背景下葡萄牙知情同意的做法,扩大与在法医DNA数据库中使用和存储遗传信息有关的传统伦理问题。本文重点介绍三个相互关联的领域:自愿为葡萄牙法医DNA数据库做出贡献的实践;向DNA捐助者提出的风险组合;以及在其个人资料中要求捐赠者的种族的伦理含义。我们认为,葡萄牙法医DNA数据库是一个有趣的案例研究,旨在重新将伦理学辩论的重点放在收集遗传信息的意义上,阐明这项活动如何重新配置​​人际关系和社会等级,法律医学和刑事司法的力量以及个人自治,隐私和个人权利的社会建设。知情同意的做法需要纳入对法医遗传数据库中收集DNA样本和DNA分析所带来的风险和不确定性的答案。

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