29 research outputs found

    Germline selection shapes human mitochondrial DNA diversity.

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    Approximately 2.4% of the human mitochondrial DNA (mtDNA) genome exhibits common homoplasmic genetic variation. We analyzed 12,975 whole-genome sequences to show that 45.1% of individuals from 1526 mother-offspring pairs harbor a mixed population of mtDNA (heteroplasmy), but the propensity for maternal transmission differs across the mitochondrial genome. Over one generation, we observed selection both for and against variants in specific genomic regions; known variants were more likely to be transmitted than previously unknown variants. However, new heteroplasmies were more likely to match the nuclear genetic ancestry as opposed to the ancestry of the mitochondrial genome on which the mutations occurred, validating our findings in 40,325 individuals. Thus, human mtDNA at the population level is shaped by selective forces within the female germ line under nuclear genetic control, which ensures consistency between the two independent genetic lineages.NIHR, Wellcome Trust, MRC, Genomics Englan

    Outsmarting Proctors with Smartwatches: A Case Study on Wearable Computing Security

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    Abstract. Many companies have recently started to offer wearable computing devices including glasses, bracelets, and watches. While this technology enables exciting new applications, it also poses new security and privacy concerns. In this work, we explore these implications and analyze the impact of one of the first networked wearable devices—smartwatches— on an academic environment. As a proof of concept, we develop an application for the Pebble smartwatch called ConTest that would allow dishonest students to inconspicuously collaborate on multiple-choice exams in real time, using a cloud-based service, a smartphone, and a client application on a smartwatch. We discuss the broader implications of this technology, suggest hardware and software approaches that can be used to prevent such attacks, and pose questions for future research
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