| Literature DB >> 28065469 |
Zhiyu Wan1, Yevgeniy Vorobeychik2, Weiyi Xia2, Ellen Wright Clayton3, Murat Kantarcioglu4, Bradley Malin5.
Abstract
Emerging scientific endeavors are creating big data repositories of data from millions of individuals. Sharing data in a privacy-respecting manner could lead to important discoveries, but high-profile demonstrations show that links between de-identified genomic data and named persons can sometimes be reestablished. Such re-identification attacks have focused on worst-case scenarios and spurred the adoption of data-sharing practices that unnecessarily impede research. To mitigate concerns, organizations have traditionally relied upon legal deterrents, like data use agreements, and are considering suppressing or adding noise to genomic variants. In this report, we use a game theoretic lens to develop more effective, quantifiable protections for genomic data sharing. This is a fundamentally different approach because it accounts for adversarial behavior and capabilities and tailors protections to anticipated recipients with reasonable resources, not adversaries with unlimited means. We demonstrate this approach via a new public resource with genomic summary data from over 8,000 individuals-the Sequence and Phenotype Integration Exchange (SPHINX)-and show that risks can be balanced against utility more effectively than with traditional approaches. We further show the generalizability of this framework by applying it to other genomic data collection and sharing endeavors. Recognizing that such models are dependent on a variety of parameters, we perform extensive sensitivity analyses to show that our findings are robust to their fluctuations.Entities:
Keywords: Electronic Medical Records and Genomics Network; Sequence and Phenotype Integration Exchange; adversarial modeling; game theory; genetic algorithm; genomic data privacy; genomic data sharing policy; re-identification risk; sensitivity analysis; summary statistics
Mesh:
Year: 2017 PMID: 28065469 PMCID: PMC5294764 DOI: 10.1016/j.ajhg.2016.12.002
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025