Systematizing Genome Privacy Research: A Privacy-Enhancing Technologies Perspective∗ Alexandros Mittos1 , Bradley Malin2 , Emiliano De Cristofaro1 arXiv:1712.02193v2 [cs.CR] 17 Aug 2018

Source URL: arxiv.org

• Biology
• Genetics
• Genomics
• Molecular biology
• Biotechnology
• DNA
• Bioinformatics
• Whole genome sequencing
• Genome-wide association study
• Single-nucleotide polymorphism
• Human genome
• Privacy

Questions Albers et alGenome Research 21:Dindel: Accurate indel calls from short-read data 1. What are some of the challenges in calling insertion-deletion polymorphisms from short read data using mappin

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Heather M. Machkovech,a,b,c Trevor Bedford,d Marc A. Suchard,e Jesse D. Blooma,c Department of Genome Sciences, University of Washington, Seattle, Washington, USAa; Medical Scientist Training Program, University of Wash

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Nucleic Acids Research, 2003, Vol. 31, No±1037 DOI: nar/gkg169 Identi®cation of pseudogenes in the Drosophila melanogaster genome Paul M. Harrison*, Duncan Milburn, Zhaolei Zhang, Paul Bertone and Mark

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Genomics and Health: Personalized Medicine Program Genome British Columbia Genomics Applied to the Management of High-Risk Acute Myelodysplastic (AML) SSH Sub-project Clinical Genome Research in the Digital Age: Managing

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Tropical Life Sciences Research, 29(1), 37–50, 2018 Genome Organization of Escherichia Phage YD-2008.s: A New Entry to Siphoviridae Family 1

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Downloaded from genome.cshlp.org on January 20, Published by Cold Spring Harbor Laboratory Press Research Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders

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Published online 07 MarchNucleic Acids Research, 2014, Vol. 42, No. 9 e75 doi: nar/gku181 Estimating telomere length from whole genome

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NIH Launches Undiagnosed Diseases Program Genome.gov - National Human Genome Research Institute Current News Releases >2008 Release: NIH Launches Undiagnosed Disease Program NIH News National Human Genome Research Instit

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Gordân et al. Genome Biology 2011, 12:R125 http://genomebiology.comR125 RESEARCH Open Access

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