486 research outputs found

    PresSafe: Barometer-based On-screen Pressure Assisted Implicit Authentication for Smartphones

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    Graphic-pattern-based implicit authentication has been successfully exploited to elevate the security of smartphones. On-screen pressure is one of the key features in such an approach since it can reveal users' touch pattern. However, state-of-the-art approaches rely on a system API to obtain on-screen pressure, which is not adequately accurate and cannot meet the demands of robust implicit authentication. To bridge this gap, we propose PresSafe, a novel implicit authentication system that utilizes the smartphone's built-in barometer sensor to measure pressure during the unlocking process, and to utilize the pressure data in authentication. A key technical challenge in utilizing barometer sensing, however, is to understand the user activity through measured pressure. To overcome this challenge, PresSafe leverages barometer data along with data from other conventional but heterogeneous ambient sensors to produce accurate and robust user activity descriptions. PresSafe utilizes a transfer-learning-based hybrid workflow to integrate user activity representation learning with a lightweight classical authentication algorithm to obtain a unified model. This approach offloads the computational cost from the terminal and addresses privacy concerns. To ensure applicability of our approach despite data heterogeneity and insufficient training data, we utilize a channel-adaptive data processing mechanism. Extensive experiments utilizing more than 70000 records from 23 volunteers in six different locations show that PresSafe achieves an FAR of 0.45%, an FRR of 0.49%, and an EER of 0.47%, which clearly demonstrate its superiority over several existing solutions.</p

    Genetic Regulatory Perturbation of Gene Expression Impacted by Genomic Introgression in Fiber Development of Allotetraploid Cotton

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    Interspecific genomic introgression is an important evolutionary process with respect to the generation of novel phenotypic diversity and adaptation. A key question is how gene flow perturbs gene expression networks and regulatory interactions. Here, an introgression population of two species of allopolyploid cotton (Gossypium) to delineate the regulatory perturbations of gene expression regarding fiber development accompanying fiber quality change is utilized. De novo assembly of the recipient parent (G. hirsutum Emian22) genome allowed the identification of genomic variation and introgression segments (ISs) in 323 introgression lines (ILs) from the donor parent (G. barbadense 3–79). It documented gene expression dynamics by sequencing 1,284 transcriptomes of developing fibers and characterized genetic regulatory perturbations mediated by genomic introgression using a multi-locus model. Introgression of individual homoeologous genes exhibiting extreme low or high expression bias can lead to a parallel expression bias in their non-introgressed duplicates, implying a shared yet divergent regulatory fate of duplicated genes following allopolyploidy. Additionally, the IL N182 with improved fiber quality is characterized, and the candidate gene GhFLAP1 related to fiber length is validated. This study outlines a framework for understanding introgression-mediated regulatory perturbations in polyploids, and provides insights for targeted breeding of superior upland cotton fiber.This article is published as Chen, Xinyuan, Xiubao Hu, Guo Li, Corrinne E. Grover, Jiaqi You, Ruipeng Wang, Zhenping Liu et al. "Genetic Regulatory Perturbation of Gene Expression Impacted by Genomic Introgression in Fiber Development of Allotetraploid Cotton." Advanced Science (2024): 2401549. doi:10.1002/advs.202401549. © 2024 The Author(s). This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited

    Sextant: Towards Ubiquitous Indoor Localization Service by Photo-Taking of the Environment

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    Mainstream indoor localization technologies rely on RF signatures that require extensive human efforts to measure and periodically recalibrate signatures. The progress to ubiquitous localization remains slow. In this study, we explore Sextant, an alternative approach that leverages environmental reference objects such as store logos. A user uses a smartphone to obtain relative position measurements to such static reference objects for the system to triangulate the user location. Sextant leverages image matching algorithms to automatically identify the chosen reference objects by photo-taking, and we propose two methods to systematically address image matching mistakes that cause large localization errors. We formulate the benchmark image selection problem, prove its NP-completeness, and propose a heuristic algorithm to solve it. We also propose a couple of geographical constraints to further infer unknown reference objects. To enable fast deployment, we propose a lightweight site survey method for service providers to quickly estimate the coordinates of reference objects. Extensive experiments have shown that Sextant prototype achieves 2-5 m accuracy at 80-percentile, comparable to the industry state-of-the-art, while covering a 150 x 75 m mall and 300 x 200 m train station requires a one time investment of only 2-3 man-hours from service providers.China NSFC [61231010, 61272027, 61421062, 61210005, 61201245]; Beijing National Science Foundation (NSF) [4142022]SCI(E)[email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]; [email protected]

    Natural killer cell-mediated shedding of ULBP2.

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    UL16 binding proteins (ULBPs) are a family of cell surface proteins that are present in transformed and stressed cells and ligands for NKG2D. Soluble NKG2D ligands have been found in sera from cancer patients with their protein concentrations correlated with poor cancer prognosis. Here we show, for the first time, that human tumor cells lost their surface expression of ULBP2, but not ULBP1 and ULBP3, during NK cell-mediated cytolysis. In contrast to spontaneous shedding of NKG2D ligands, NK cytolysis-mediated shedding of ULBP2 was linked to target cell apoptosis, although both resulted from metalloproteinase cleavages. Inhibition of ULBP2 shedding by a metalloproteinase inhibitor BB-94 lead to reduced NK cell-mediated cytotoxicity and cytokine production. These results illustrate a regulation of NK cell effector functions through cytolysis-induced NKG2D ligand shedding. Consequently, compounds inhibiting NKG2D ligand shedding may offer therapeutic means to reduce excessive pathogenic NK cell activities
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