6,768 research outputs found

    Detection of fingerprint alterations using deep convolutional neural networks

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    Fingerprint alteration is a challenge that poses enormous security risks. As a result, many research efforts in the scientific community have attempted to address this issue. However, non-existence of publicly available datasets that contain obfuscation and distortion of fingerprints makes it difficult to identify the type of alteration. In this work we present the publicly available Sokoto-Coventry Fingerprints Dataset (SOCOFing), which provides ten fingerprints for 600 different subjects, as well as gender, hand and finger name for each image, among other unique characteristics. We also provide a total of 55,249 images with three levels of alteration for Z-cut, obliteration and central rotation synthetic alterations, which are the most common types of obfuscation and distortion. In addition, this paper proposes a Convolutional Neural Network (CNN) to identify these alterations. The proposed CNN model achieves a classification accuracy rate of 98.55%. Results are also compared with a residual CNN model pre-trained on ImageNet, which produces an accuracy of 99.88%

    Non-monotonic magnetic field and density dependence of in-plane magnetoresistance in dilute two-dimensional holes in GaAs/AlGaAs

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    We studied low temperature (T=50mK) in-plane magnetoresistance of a dilute two-dimensional hole system in GaAs/AlGaAs heterostructure that exhibits an apparent metal-insulator transition. We found an anisotropic magnetoresistance, which changes dramatically at high in-plane fields (B_{\parallel}\agt5T) as the hole density is varied. At high densities where the system behaves metallic at B=0B_{\parallel}=0, the transverse magnetoresistance is larger than the longitudinal magnetoresistance. With decreasing the hole density the difference becomes progressively smaller, and at densities near the "critical" density and lower, the longitudinal magnetoresistance becomes larger than the transverse magnetoresistance

    Resonance Damping in Ferromagnets and Ferroelectrics

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    The phenomenological equations of motion for the relaxation of ordered phases of magnetized and polarized crystal phases can be developed in close analogy with one another. For the case of magnetized systems, the driving magnetic field intensity toward relaxation was developed by Gilbert. For the case of polarized systems, the driving electric field intensity toward relaxation was developed by Khalatnikov. The transport times for relaxation into thermal equilibrium can be attributed to viscous sound wave damping via magnetostriction for the magnetic case and electrostriction for the polarization case.Comment: 5 pages no figures ReVTeX

    Enabling smart city resilience: Post-disaster response and structural health monitoring

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    The concept of Smart Cities has been introduced to categorize a vast area of activities to enhance the quality of life of citizens. A central feature of these activities is the pervasive use of Information and Communication Technologies (ICT), helping cities to make better use of limited resources. Indeed, the ASCE Vision for Civil Engineering in 2025 (ASCE 2007) portends a future in which engineers will rely on and leverage real-time access to a living database, sensors, diagnostic tools, and other advanced technologies to ensure that informed decisions are made. However, these advances in technology take place against a backdrop of the deterioration of infrastructure, in addition to natural and human-made disasters. Moreover, recent events constantly remind us of the tremendous devastation that natural and human-made disasters can wreak on society. As such, emergency response procedures and resilience are among the crucial dimensions of any Smart City plan. The U.S. Department of Homeland Security (DHS) has recently launched plans to invest $50 million to develop cutting-edge emergency response technologies for Smart Cities. Furthermore, after significant disasters have taken place, it is imperative that emergency facilities and evacuation routes, including bridges and highways, be assessed for safety. The objective of this research is to provide a new framework that uses commercial off-the-shelf (COTS) devices such as smartphones, digital cameras, and unmanned aerial vehicles to enhance the functionality of Smart Cities, especially with respect to emergency response and civil infrastructure monitoring/assessment. To achieve this objective, this research focuses on post-disaster victim localization and assessment, first responder tracking and event localization, and vision-based structural monitoring/assessment, including the use of unmanned aerial vehicles (UAVs). This research constitutes a significant step toward the realization of Smart City Resilience.National Science Foundation Grant No. 1030454Association of American RailroadsOpe

    CATNAP: a tool to compile, analyze and tally neutralizing antibody panels

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    CATNAP (Compile, Analyze and Tally NAb Panels) is a new web server at Los Alamos HIV Database, created to respond to the newest advances in HIV neutralizing antibody research. It is a comprehensive platform focusing on neutralizing antibody potencies in conjunction with viral sequences. CATNAP integrates neutralization and sequence data from published studies, and allows users to analyze that data for each HIV Envelope protein sequence position and each antibody. The tool has multiple data retrieval and analysis options. As input, the user can pick specific antibodies and viruses, choose a panel from a published study, or supply their own data. The output superimposes neutralization panel data, virus epidemiological data, and viral protein sequence alignments on one page, and provides further information and analyses. The user can highlight alignment positions, or select antibody contact residues and view position-specific information from the HIV databases. The tool calculates tallies of amino acids and N-linked glycosylation motifs, counts of antibody-sensitive and -resistant viruses in conjunction with each amino acid or N-glycosylation motif, and performs Fisher's exact test to detect potential positive or negative amino acid associations for the selected antibody. Website name: CATNAP (Compile, Analyze and Tally NAb Panels). Website address: http://hiv.lanl.gov/catnap

    Muscle Fatigue Analysis Using OpenSim

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    In this research, attempts are made to conduct concrete muscle fatigue analysis of arbitrary motions on OpenSim, a digital human modeling platform. A plug-in is written on the base of a muscle fatigue model, which makes it possible to calculate the decline of force-output capability of each muscle along time. The plug-in is tested on a three-dimensional, 29 degree-of-freedom human model. Motion data is obtained by motion capturing during an arbitrary running at a speed of 3.96 m/s. Ten muscles are selected for concrete analysis. As a result, the force-output capability of these muscles reduced to 60%-70% after 10 minutes' running, on a general basis. Erector spinae, which loses 39.2% of its maximal capability, is found to be more fatigue-exposed than the others. The influence of subject attributes (fatigability) is evaluated and discussed

    Ac transport studies in polymers by a resistor network and transfer matrix approaches: application to polyaniline

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    A statistical model of resistor network is proposed to describe a polymer structure and to simulate the real and imaginary components of its ac resistivity. It takes into account the polydispersiveness of the material as well as intrachain and interchain charge transport processes. By the application of a transfer matrix technique, it reproduces ac resistivity measurements carried out with polyaniline films in different doping degrees and at different temperatures. Our results indicate that interchain processes govern the resistivity behavior in the low frequency region while, for higher frequencies, intrachain mechanisms are dominant.Comment: LaTeX file, 15 pages, 5 ps figures, to appear in Phys. Rev.

    Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism.

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    Recent studies have identified both recessive and dominant forms of mitochondrial disease that result from ATAD3A variants. The recessive form includes subjects with biallelic deletions mediated by non-allelic homologous recombination. We report five unrelated neonates with a lethal metabolic disorder characterized by cardiomyopathy, corneal opacities, encephalopathy, hypotonia, and seizures in whom a monoallelic reciprocal duplication at the ATAD3 locus was identified. Analysis of the breakpoint junction fragment indicated that these 67 kb heterozygous duplications were likely mediated by non-allelic homologous recombination at regions of high sequence identity in ATAD3A exon 11 and ATAD3C exon 7. At the recombinant junction, the duplication allele produces a fusion gene derived from ATAD3A and ATAD3C, the protein product of which lacks key functional residues. Analysis of fibroblasts derived from two affected individuals shows that the fusion gene product is expressed and stable. These cells display perturbed cholesterol and mitochondrial DNA organization similar to that observed for individuals with severe ATAD3A deficiency. We hypothesize that the fusion protein acts through a dominant-negative mechanism to cause this fatal mitochondrial disorder. Our data delineate a molecular diagnosis for this disorder, extend the clinical spectrum associated with structural variation at the ATAD3 locus, and identify a third mutational mechanism for ATAD3 gene cluster variants. These results further affirm structural variant mutagenesis mechanisms in sporadic disease traits, emphasize the importance of copy number analysis in molecular genomic diagnosis, and highlight some of the challenges of detecting and interpreting clinically relevant rare gene rearrangements from next-generation sequencing data

    Combinations of β-lactam or aminoglycoside antibiotics with plectasin are synergistic against methicillin-sensitive and methicillin-resistant Staphylococcus aureus.

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    Bacterial infections remain the leading killer worldwide which is worsened by the continuous emergence of antibiotic resistance. In particular, methicillin-sensitive (MSSA) and methicillin-resistant Staphylococcus aureus (MRSA) are prevalent and the latter can be difficult to treat. The traditional strategy of novel therapeutic drug development inevitably leads to emergence of resistant strains, rendering the new drugs ineffective. Therefore, rejuvenating the therapeutic potentials of existing antibiotics offers an attractive novel strategy. Plectasin, a defensin antimicrobial peptide, potentiates the activities of other antibiotics such as β-lactams, aminoglycosides and glycopeptides against MSSA and MRSA. We performed in vitro and in vivo investigations to test against genetically diverse clinical isolates of MSSA (n = 101) and MRSA (n = 115). Minimum inhibitory concentrations (MIC) were determined by the broth microdilution method. The effects of combining plectasin with β-lactams, aminoglycosides and glycopeptides were examined using the chequerboard method and time kill curves. A murine neutropenic thigh model and a murine peritoneal infection model were used to test the effect of combination in vivo. Determined by factional inhibitory concentration index (FICI), plectasin in combination with aminoglycosides (gentamicin, neomycin or amikacin) displayed synergistic effects in 76-78% of MSSA and MRSA. A similar synergistic response was observed when plectasin was combined with β-lactams (penicillin, amoxicillin or flucloxacillin) in 87-89% of MSSA and MRSA. Interestingly, no such interaction was observed when plectasin was paired with vancomycin. Time kill analysis also demonstrated significant synergistic activities when plectasin was combined with amoxicillin, gentamicin or neomycin. In the murine models, plectasin at doses as low as 8 mg/kg augmented the activities of amoxicillin and gentamicin in successful treatment of MSSA and MRSA infections. We demonstrated that plectasin strongly rejuvenates the therapeutic potencies of existing antibiotics in vitro and in vivo. This is a novel strategy that can have major clinical implications in our fight against bacterial infections
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