Membership Privacy in MicroRNA-based Studies

M. Backes, Pascal Berrang, Mathias Humbert, Praveen Manoharan
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引用次数: 134

Abstract

The continuous decrease in cost of molecular profiling tests is revolutionizing medical research and practice, but it also raises new privacy concerns. One of the first attacks against privacy of biological data, proposed by Homer et al. in 2008, showed that, by knowing parts of the genome of a given individual and summary statistics of a genome-based study, it is possible to detect if this individual participated in the study. Since then, a lot of work has been carried out to further study the theoretical limits and to counter the genome-based membership inference attack. However, genomic data are by no means the only or the most influential biological data threatening personal privacy. For instance, whereas the genome informs us about the risk of developing some diseases in the future, epigenetic biomarkers, such as microRNAs, are directly and deterministically affected by our health condition including most common severe diseases. In this paper, we show that the membership inference attack also threatens the privacy of individuals contributing their microRNA expressions to scientific studies. Our results on real and public microRNA expression data demonstrate that disease-specific datasets are especially prone to membership detection, offering a true-positive rate of up to 77% at a false-negative rate of less than 1%. We present two attacks: one relying on the L_1 distance and the other based on the likelihood-ratio test. We show that the likelihood-ratio test provides the highest adversarial success and we derive a theoretical limit on this success. In order to mitigate the membership inference, we propose and evaluate both a differentially private mechanism and a hiding mechanism. We also consider two types of adversarial prior knowledge for the differentially private mechanism and show that, for relatively large datasets, this mechanism can protect the privacy of participants in miRNA-based studies against strong adversaries without degrading the data utility too much. Based on our findings and given the current number of miRNAs, we recommend to only release summary statistics of datasets containing at least a couple of hundred individuals.
基于microrna的研究中的成员隐私
分子分析测试成本的持续下降正在彻底改变医学研究和实践,但它也引发了新的隐私问题。荷马等人在2008年提出的对生物数据隐私的第一次攻击表明,通过了解给定个体的部分基因组和基于基因组的研究的汇总统计数据,可以检测该个体是否参与了该研究。从那时起,人们进行了大量的工作来进一步研究理论限制和对抗基于基因组的成员推理攻击。然而,基因组数据绝不是威胁个人隐私的唯一或最具影响力的生物数据。例如,基因组告诉我们未来患某些疾病的风险,而表观遗传生物标志物,如microrna,直接和决定性地受到我们的健康状况的影响,包括最常见的严重疾病。在本文中,我们证明了成员推理攻击也威胁到为科学研究提供其microRNA表达的个人的隐私。我们对真实和公开的microRNA表达数据的研究结果表明,疾病特异性数据集特别容易进行成员检测,其真阳性率高达77%,假阴性率低于1%。我们提出了两种攻击:一种依赖于l1距离,另一种基于似然比检验。我们表明,似然比检验提供了最高的对抗性成功,我们推导出了这种成功的理论极限。为了减轻成员推理,我们提出并评估了一种差分私有机制和一种隐藏机制。我们还考虑了差异私有机制的两种类型的对抗性先验知识,并表明,对于相对较大的数据集,该机制可以保护基于mirna的研究中参与者的隐私,而不会降低数据效用太多。基于我们的发现和目前mirna的数量,我们建议只发布包含至少几百个个体的数据集的汇总统计数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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