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Questioning the limits of genomic privacy

机译:质疑基因组隐私的局限性

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摘要

Recently, Im et al. presented a method that can infer an individual's participation in a study when regression coefficients from quantitative phenotypes are available. They demonstrated that in an era of increasing use of high-throughput technologies to integrate multiple-omics data sets, the "problem of identifiability" necessitates the creation of robust methods (e.g., an annual certification process) that facilitate broad dissemination of study results without compromising a participant's privacy. In this letter, we would like to qualify the conclusions of Im et al., and several other commentators,2"5 by illustrating that (1) despite the perceived ease of reidenti&cation, anonymity (and genomic privacy in general, which subsumes anonymity and identifiability as critical elements of informational control) remains a valid and vital concept and (2) technologies and models currently exist that facilitate dissemination of useful health data without compromising privacy.
机译:最近,Im等人。提出了一种方法,当可以从定量表型获得回归系数时,可以推断个人参与研究。他们表明,在一个越来越多地使用高通量技术来集成多组学数据集的时代,“可识别性问题”需要创建可靠的方法(例如,年度认证流程)来促进研究结果的广泛传播,而又不会损害参与者的隐私。在这封信中,我们想证明Im等人和其他几位评论员的结论[2] [5],方法是说明(1)尽管人们认为重新识别,匿名性和基因组隐私通常较为容易,但其中包括匿名性和可识别性作为信息控制的关键要素)仍然是一个有效且至关重要的概念,并且(2)当前存在的技术和模型可促进有用健康数据的传播而不损害隐私。

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