Patient-controlled encrypted genomic data: an approach to advance clinical genomics
Published 2012 View Full Article
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Title
Patient-controlled encrypted genomic data: an approach to advance clinical genomics
Authors
Keywords
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Journal
BMC Medical Genomics
Volume 5, Issue 1, Pages -
Publisher
Springer Nature
Online
2012-07-21
DOI
10.1186/1755-8794-5-31
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Note: Only part of the references are listed.- Family-Based Association Studies for Next-Generation Sequencing
- (2012) Yun Zhu et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2011) Richard R Sharp GENETICS IN MEDICINE
- A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®)
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- (2011) Adriano Jimenez-Escrig et al. MUSCLE & NERVE
- Charting a course for genomic medicine from base pairs to bedside
- (2011) Eric D. Green et al. NATURE
- MutaDATABASE: a centralized and standardized DNA variation database
- (2011) Sherri Bale et al. NATURE BIOTECHNOLOGY
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- Family-based designs for genome-wide association studies
- (2011) Jurg Ott et al. NATURE REVIEWS GENETICS
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- (2011) Michael J. Bamshad et al. NATURE REVIEWS GENETICS
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- (2010) R Dorfman et al. CLINICAL GENETICS
- Personal genome sequencing: current approaches and challenges
- (2010) M. Snyder et al. GENES & DEVELOPMENT
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- Challenges in the clinical application of whole-genome sequencing
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- (2010) Richard M. Durbin et al. NATURE
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- Personalized genomic information: preparing for the future of genetic medicine
- (2010) Alan E. Guttmacher et al. NATURE REVIEWS GENETICS
- Gene–environment-wide association studies: emerging approaches
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- (2010) David Warde-Farley et al. NUCLEIC ACIDS RESEARCH
- Ethical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practice
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- (2009) Erika Check Hayden NATURE
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- (2009) Soumya Raychaudhuri et al. NATURE GENETICS
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- (2009) M. R. Lincoln et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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