PICOTEES:一项保护隐私的在线服务,为中国儿童群体的遗传诊断变异进行表型探索。

Xinran Dong, Yulan Lu, Lanting Guo, Chuan Li, Qi Ni, Bingbing Wu, Huijun Wang, Lin Yang, Songyang Wu, Qi Sun, Hao Zheng, Wenhao Zhou, Shuang Wang
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引用次数: 0

摘要

生物医学数据资源的增长引发了潜在的隐私问题和基因信息泄露的风险。例如,外显子组测序通过网络服务比较数据来帮助临床决策,但它需要用户和提供者之间的高度信任。为了缓解隐私问题,最常用的策略是匿名化敏感数据。不幸的是,研究表明,匿名化不足以抵御再识别攻击。最近,隐私保护技术被应用于在保护生物医学数据隐私的同时保持应用效用。我们提出了PICOTEES框架,这是一种保护隐私的遗传诊断变异表型探索在线服务。PICOTEES通过利用可信执行环境技术,实现了对单个变体表型谱的隐私保护查询,该技术可以保护用户查询信息、后端模型和数据以及最终结果的隐私。我们通过探索生物信息学数据集来展示PICOTEES的实用性和性能。该数据集来自中国复旦大学儿童医院的20909名基因检测患者,其中3152508个变异株,主要是中国汉族(>99.9%)。我们的查询结果产生了大量未报告的诊断变异株和先前报告的致病性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PICOTEES: a privacy-preserving online service of phenotype exploration for genetic-diagnostic variants from Chinese children cohorts.

The growth in biomedical data resources has raised potential privacy concerns and risks of genetic information leakage. For instance, exome sequencing aids clinical decisions by comparing data through web services, but it requires significant trust between users and providers. To alleviate privacy concerns, the most commonly used strategy is to anonymize sensitive data. Unfortunately, studies have shown that anonymization is insufficient to protect against reidentification attacks. Recently, privacy-preserving technologies have been applied to preserve application utility while protecting the privacy of biomedical data. We present the PICOTEES framework, a privacy-preserving online service of phenotype exploration for genetic-diagnostic variants (https://birthdefectlab.cn:3000/). PICOTEES enables privacy-preserving queries of the phenotype spectrum for a single variant by utilizing trusted execution environment technology, which can protect the privacy of the user's query information, backend models, and data, as well as the final results. We demonstrate the utility and performance of PICOTEES by exploring a bioinformatics dataset. The dataset is from a cohort containing 20,909 genetic testing patients with 3,152,508 variants from the Children's Hospital of Fudan University in China, dominated by the Chinese Han population (>99.9%). Our query results yield a large number of unreported diagnostic variants and previously reported pathogenicity.

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