基于高阶SNV相关性的推理攻击量化基因组隐私

Sahel Shariati Samani, Zhicong Huang, Erman Ayday, M. Elliot, J. Fellay, J. Hubaux, Z. Kutalik
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引用次数: 35

摘要

随着基因组数据的广泛应用,基因组数据隐私问题成为遗传学家、生物信息学家和安全隐私专家跨学科研究的热点。已经确定了针对基因组数据的实际攻击,从而打破了为医学研究提供基因组数据或仅仅在网上分享数据的个人对隐私的期望。令人沮丧的是,这个问题可能会变得更糟。现有的基因组隐私泄露依赖于低阶SNV(单核苷酸变异)相关性。我们的工作表明,如果利用高阶相关性,可以设计出更强大的攻击。我们利用基于不同基因组数据模型的不同SNV相关性,并将其应用于对隐藏SNV的个体基因型数据的推理攻击,从而证实了这一担忧。我们还表明,低阶模型的行为与真实的基因组数据非常不同,因此不应该依赖于隐私保护解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantifying Genomic Privacy via Inference Attack with High-Order SNV Correlations
As genomic data becomes widely used, the problem of genomic data privacy becomes a hot interdisciplinary research topic among geneticists, bioinformaticians and security and privacy experts. Practical attacks have been identified on genomic data, and thus break the privacy expectations of individuals who contribute their genomic data to medical research, or simply share their data online. Frustrating as it is, the problem could become even worse. Existing genomic privacy breaches rely on low-order SNV (Single Nucleotide Variant) correlations. Our work shows that far more powerful attacks can be designed if high-order correlations are utilized. We corroborate this concern by making use of different SNV correlations based on various genomic data models and applying them to an inference attack on individuals' genotype data with hidden SNVs. We also show that low-order models behave very differently from real genomic data and therefore should not be relied upon for privacy-preserving solutions.
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