Research ethics. The complexities of genomic identifiability.
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Evolving approaches to the ethical management of genomic dataGenetic research on biospecimens poses minimal riskExploring pathways to trust: a tribal perspective on data sharingQuantification of private information leakage from phenotype-genotype data: linking attacksA vision for ubiquitous sequencingSecurely measuring the overlap between private datasets with cryptosetsThe risk of re-identification versus the need to identify individuals in rare disease researchIdentifiability and privacy in pluripotent stem cell researchEthical considerations of research policy for personal genome analysis: the approach of the Genome Science Project in JapanNext-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effectsSize matters: how population size influences genotype-phenotype association studies in anonymized dataConsenting for current genetic research: is Canadian practice adequate?SecureMA: protecting participant privacy in genetic association meta-analysisOpen access data sharing in genomic researchData use under the NIH GWAS data sharing policy and future directionsEnsuring privacy in the study of pathogen geneticsRoutes for breaching and protecting genetic privacyOur genomes today: time to be clearA mechanism for controlled access to GWAS data: experience of the GAIN Data Access CommitteeAn open access pilot freely sharing cancer genomic data from participants in Texas.Pediatric data sharing in genomic research: attitudes and preferences of parents.Differentially private genome data dissemination through top-down specializationBig Data in medical research and EU data protection law: challenges to the consent or anonymise approachMolecular digital pathology: progress and potential of exchanging molecular data.Expanding Access to Large-Scale Genomic Data While Promoting Privacy: A Game Theoretic Approach.A gene-specific method for predicting hemophilia-causing point mutations.Translating personalized medicine using new genetic technologies in clinical practice: the ethical issuesGenomic cloud computing: legal and ethical points to considerMultikernel linear mixed models for complex phenotype prediction.Policy uncertainty, sequencing, and cell lines.The Henrietta Lacks legacy grows.Lessons from HeLa Cells: The Ethics and Policy of Biospecimens.Biospecimen policy: Family mattersPolicy recommendations for addressing privacy challenges associated with cell-based research and interventions.Confidentiality in Biobanking Research: A Comparison of Donor and Nondonor Families' Understanding of Risks.A Primer on Infectious Disease Bacterial GenomicsPast, Present, and Future of Informed Consent in Pain and Genomics Research: Challenges Facing Global Medical Community.Genome privacy: challenges, technical approaches to mitigate risk, and ethical considerations in the United States.An overview of human genetic privacy.Ethical issues in pain and omics research. Some points to start the debate.
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Research ethics. The complexities of genomic identifiability.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Research ethics. The complexities of genomic identifiability.
@en
Research ethics. The complexities of genomic identifiability.
@nl
type
label
Research ethics. The complexities of genomic identifiability.
@en
Research ethics. The complexities of genomic identifiability.
@nl
prefLabel
Research ethics. The complexities of genomic identifiability.
@en
Research ethics. The complexities of genomic identifiability.
@nl
P2093
P2860
P356
P1433
P1476
Research ethics. The complexities of genomic identifiability.
@en
P2093
Judith H Greenberg
Laura L Rodriguez
Lisa D Brooks
P2860
P304
P356
10.1126/SCIENCE.1234593
P407
P577
2013-01-01T00:00:00Z