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Opportunities and Challenges in Interpreting and Sharing Personal Genomes

机译:解释和分享个人基因组的机遇与挑战

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摘要

The 2019 “Personal Genomes: Accessing, Sharing and Interpretation” conference (Hinxton, UK, 11–12 April 2019) brought together geneticists, bioinformaticians, clinicians and ethicists to promote openness and ethical sharing of personal genome data while protecting the privacy of individuals. The talks at the conference focused on two main topic areas: (1) Technologies and Applications, with emphasis on personal genomics in the context of healthcare. The issues discussed ranged from new technologies impacting and enabling the field, to the interpretation of personal genomes and their integration with other data types. There was particular emphasis and wide discussion on the use of polygenic risk scores to inform precision medicine. (2) Ethical, Legal, and Social Implications, with emphasis on genetic privacy: How to maintain it, how much privacy is possible, and how much privacy do people want? Talks covered the full range of genomic data visibility, from open access to tight control, and diverse aspects of balancing benefits and risks, data ownership, working with individuals and with populations, and promoting citizen science. Both topic areas were illustrated and informed by reports from a wide variety of ongoing projects, which highlighted the need to diversify global databases by increasing representation of understudied populations.
机译:2019年的“个人基因组:访问,共享和解释”会议(英国亨克斯顿,2019年4月11日至12日)召集了遗传学家,生物信息学家,临床医生和伦理学家,以促进开放性和伦理共享个人基因组数据,同时保护个人隐私。会议的演讲集中在两个主要主题领域:(1)技术和应用,重点是医疗保健领域的个人基因组学。讨论的问题范围从影响和推动该领域的新技术到个人基因组的解释及其与其他数据类型的集成。关于使用多基因风险评分为精密医学提供信息特别强调和广泛讨论。 (2)伦理,法律和社会影响,重点在于基因隐私:如何维护遗传密码,可能有多少隐私以及人们想要多少隐私?讲座涵盖了从开放获取到严格控制的全范围的基因组数据可见性,以及平衡收益和风险,数据所有权,与个人和人群合作以及促进公民科学的各个方面。这两个主题领域都通过大量正在进行的项目的报告得到说明和介绍,这些报告强调了通过增加对被研究人群的代表性来使全球数据库多样化的必要性。

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