Secure Sharing of Clinical History & Genetic Data: Empowering Predictive Pers. Me
Secure Sharing of Clinical History & Genetic Data: Empowering Predictive Pers. Me
批准号:
8729006
负责人:
C DAVID PAGE, JR.
金额:
$55.47万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-15 至 2016-08-31
关键词:
AcuteAddressAlgorithmsCaringClinicClinicalCloud ComputingComplexComputer AssistedComputer SecurityComputer softwareComputerized Medical RecordComputersConfidentialityDataData AnalysesData SetDevelopmentDiseaseDoseEnsureEnvironmentEvaluationGeneticGenetic DatabasesGenomicsGoalsHealthHealth PersonnelIndividualInstitutionLeadMachine LearningMedicalMedical GeneticsMedical RecordsMedicineMiningModelingOperating SystemOutputPatientsPrivacyPublicationsPublishingRecording of previous eventsResearch PersonnelResourcesRiskRunningSecureSecurityStructureSystemTechnologyWarfarinWisconsinWorkbasedata managementdata miningdata sharingdesignempoweredexperiencelaptopmeetingsnovelpatient privacypredictive modelingprototypevirtual
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Computer-assisted medicine is at a crossroads: medical care requires accurate data, but making such data widely available can create unacceptable risks to the privacy of individual patients. This tension between utility and privacy is especially acute in predictive personalized medicine (PPM). PPM holds the promise of making treatment decisions tailored to the individual based on her or his particular genetics and clinical history. Making PPM a reality requires running statistical, data mining and machine learning algorithms on combined genetic, clinical and demographic data to construct predictive models. Access to such data directly competes with the need for healthcare providers to protect the privacy of each patient's data, thus creating a tradeoff between model efficacy and privacy. Thus we find ourselves in an unfortunate standoff: significant medical advances that would result from more powerful mining of the data by a wider variety of researchers are hindered by significant privacy concerns on behalf of the patients represented in the data set. In this proposed work, we seek to develop and evaluate technology to resolve this standoff, enabling health practitioners and researchers to compute on privacy-sensitive medical records in order to make treatment decisions or create accurate models, while protecting patient privacy. We will evaluate our approach on a de-identified actual electronic medical record, with an average of 29 years of clinical history on each patient, and with detailed genetic data (650K SNPs) available for a subset of 5000 of the patients. This data set is available to us now through the Wisconsin Genomics Initiative, but only on a computer at the Marshfield Clinic. If successful our approach will make possible the sharing of this cutting-edge data set, and others like it that are now in development, including our ability to analyze this data at UW-Madison where we have thousands of processors available in our Condor pool. Our privacy approach integrates secure data access environments, including those appropriate to the use of laptops and cloud computing, with novel anonymization algorithms providing differential privacy guarantees for data and/or published results of data analysis. To this end, our specific aims are as follows:
AIM 1: Develop and deploy a secure local environment that, in combination with secure network functionality, will ensure end-to-end security and privacy for electronic medical records and biomedical datasets shared between clinical institutions and researchers.
AIM 2: Develop and deploy a secure virtual environment to allow large-scale, privacy-preserving data analysis "in the cloud."
AIM 3: Develop and evaluate privacy-preserving data mining algorithms for use with original (not anonymized) data sets consisting of electronic medical records and genetic data.
AIM 4: Develop and evaluate anonymizing data publishing algorithms and privacy guarantees that are appropriate to the complex structure present in electronic medical records with genetic data.
期刊论文(10)
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DOI:
10.14722/ndss.2014.23323
发表时间:
2014-02
期刊:
NDSS symposium
影响因子:
--
作者:
[Martin Georgiev;S. Jana;Vitaly Shmatikov]
通讯作者:
Martin Georgiev;S. Jana;Vitaly Shmatikov
DOI:
10.1109/sp.2013.29
发表时间:
2013-12-31
期刊:
Proceedings. IEEE Symposium on Security and Privacy
影响因子:
--
作者:
[Lee MZ, Dunn AM, Katz J, Waters B, Witchel E]
通讯作者:
Witchel E
Application-Defined Decentralized Access Control.
应用程序定义的分散访问控制。
DOI:
--
发表时间:
2014
期刊:
Proceedings of the USENIX ... annual Technical Conference. USENIX Technical Conference
影响因子:
--
作者:
[Xu,Yuanzhong, Dunn,AlanM, Hofmann,OwenS, Lee,MichaelZ, Mehdi,SyedAkbar, Witchel,Emmett]
通讯作者:
Witchel,Emmett
DOI:
10.1145/2451116.2451146
发表时间:
2013
期刊:
ASPLOS ... proceedings. International Conference on Architectural Support for Programming Languages and Operating Systems
影响因子:
--
作者:
[Hofmann OS, Kim S, Dunn AM, Lee MZ, Witchel E]
通讯作者:
Witchel E
On Optimal Differentially Private Mechanisms for Count-Range Queries.
关于计数范围查询的最优差分私有机制。
DOI:
10.1145/2448496.2448528
发表时间:
2013
期刊:
Database theory-- ICDT : International Conference ... proceedings. International Conference on Database Theory
影响因子:
--
作者:
[Zeng,Chen, Cai,Jin-Yi, Lu,Pinyan, Naughton,JeffreyF]
通讯作者:
Naughton,JeffreyF
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Machine Learning for Identifying Adverse Drug Events
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批准号:8085232
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资助金额:$54.87万
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负责人:C DAVID PAGE, JR.
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Machine Learning for Identifying Adverse Drug Events
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资助金额:$33.71万
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Machine Learning for Identifying Adverse Drug Events
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批准号:8466993
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资助金额:$52.08万
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Secure Sharing of Clinical History & Genetic Data: Empowering Predictive Pers. Me
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批准号:8333324
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项目类别:
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资助金额:$54.51万
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负责人:C DAVID PAGE, JR.
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Secure Sharing of Clinical History & Genetic Data: Empowering Predictive Pers. Me
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批准号:8085051
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项目类别:
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资助金额:$58.88万
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财政年份:2011
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负责人:C DAVID PAGE, JR.
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依托单位:
Cancer Informatics
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批准号:7491895
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负责人:C DAVID PAGE, JR.
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Cancer Informatics
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资助金额:$37.51万
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财政年份:--
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负责人:C DAVID PAGE, JR.
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依托单位:
Cancer Informatics
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批准号:7726694
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资助金额:$35.21万
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财政年份:--
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资助金额:$35.61万
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海外基金