214 research outputs found

    MHSP in reversed-biased operation mode for ion blocking in gas-avalanche multipliers

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    We present recent results on the operation of gas-avalanche detectors comprising a cascade of gas electron multipliers (GEMs) and Micro-Hole and Strip Plates (MHSPs) multiplier operated in reversed-bias (R-MHSP) mode. The operation mechanism of the R-MHSP is explained and its potential contribution to ion-backflow (IBF) reduction is demonstrated. IBF values of 4E-3 were obtained in cascaded R-MHSP and GEM multipliers at gains of about 1E+4, though at the expense of reduced effective gain in the first R- MHSP multiplier in the cascade.Comment: 23 pages, 8 figure

    Interactive Content-Based Image Retrieval with Deep Neural Networks

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    Detectors for Energy-Resolved Fast Neutron Imaging

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    Two detectors for energy-resolved fast-neutron imaging in pulsed broad-energy neutron beams are presented. The first one is a neutron-counting detector based on a solid neutron converter coupled to a gaseous electron multiplier (GEM). The second is an integrating imaging technique, based on a scintillator for neutron conversion and an optical imaging system with fast framing capability

    Enumerating Isolated Cliques in Temporal Networks

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    Isolation is a concept from the world of clique enumeration that is mostly used to model communities that do not have much contact to the outside world. Herein, a clique is considered isolated if it has few edges connecting it to the rest of the graph. Motivated by recent work on enumerating cliques in temporal networks, we lift the isolation concept to this setting. We discover that the addition of the time dimension leads to six distinct natural isolation concepts. Our main contribution is the development of fixed-parameter enumeration algorithms for five of these six clique types employing the parameter "degree of isolation". On the empirical side, we implement and test these algorithms on (temporal) social network data, obtaining encouraging preliminary results

    Stimulus-dependent maximum entropy models of neural population codes

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    Neural populations encode information about their stimulus in a collective fashion, by joint activity patterns of spiking and silence. A full account of this mapping from stimulus to neural activity is given by the conditional probability distribution over neural codewords given the sensory input. To be able to infer a model for this distribution from large-scale neural recordings, we introduce a stimulus-dependent maximum entropy (SDME) model---a minimal extension of the canonical linear-nonlinear model of a single neuron, to a pairwise-coupled neural population. The model is able to capture the single-cell response properties as well as the correlations in neural spiking due to shared stimulus and due to effective neuron-to-neuron connections. Here we show that in a population of 100 retinal ganglion cells in the salamander retina responding to temporal white-noise stimuli, dependencies between cells play an important encoding role. As a result, the SDME model gives a more accurate account of single cell responses and in particular outperforms uncoupled models in reproducing the distributions of codewords emitted in response to a stimulus. We show how the SDME model, in conjunction with static maximum entropy models of population vocabulary, can be used to estimate information-theoretic quantities like surprise and information transmission in a neural population.Comment: 11 pages, 7 figure

    Metabolic labeling of RNA uncovers principles of RNA production and degradation dynamics in mammalian cells

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    available in PMC 2011 November 01.Cellular RNA levels are determined by the interplay of RNA production, processing and degradation. However, because most studies of RNA regulation do not distinguish the separate contributions of these processes, little is known about how they are temporally integrated. Here we combine metabolic labeling of RNA at high temporal resolution with advanced RNA quantification and computational modeling to estimate RNA transcription and degradation rates during the response of mouse dendritic cells to lipopolysaccharide. We find that changes in transcription rates determine the majority of temporal changes in RNA levels, but that changes in degradation rates are important for shaping sharp 'peaked' responses. We used sequencing of the newly transcribed RNA population to estimate temporally constant RNA processing and degradation rates genome wide. Degradation rates vary significantly between genes and contribute to the observed differences in the dynamic response. Certain transcripts, including those encoding cytokines and transcription factors, mature faster. Our study provides a quantitative approach to study the integrative process of RNA regulation.Human Frontier Science Program (Strasbourg, France)Howard Hughes Medical InstituteBurroughs Wellcome Fund (Career Award at the Scientific Interface

    Using the information embedded in the testing sample to break the limits caused by the small sample size in microarray-based classification

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    <p>Abstract</p> <p>Background</p> <p>Microarray-based tumor classification is characterized by a very large number of features (genes) and small number of samples. In such cases, statistical techniques cannot determine which genes are correlated to each tumor type. A popular solution is the use of a subset of pre-specified genes. However, molecular variations are generally correlated to a large number of genes. A gene that is not correlated to some disease may, by combination with other genes, express itself.</p> <p>Results</p> <p>In this paper, we propose a new classiification strategy that can reduce the effect of over-fitting without the need to pre-select a small subset of genes. Our solution works by taking advantage of the information embedded in the testing samples. We note that a well-defined classification algorithm works best when the data is properly labeled. Hence, our classification algorithm will discriminate all samples best when the testing sample is assumed to belong to the correct class. We compare our solution with several well-known alternatives for tumor classification on a variety of publicly available data-sets. Our approach consistently leads to better classification results.</p> <p>Conclusion</p> <p>Studies indicate that thousands of samples may be required to extract useful statistical information from microarray data. Herein, it is shown that this problem can be circumvented by using the information embedded in the testing samples.</p

    Development Trends of White Matter Connectivity in the First Years of Life

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    The human brain is organized into a collection of interacting networks with specialized functions to support various cognitive functions. Recent research has reached a consensus that the brain manifests small-world topology, which implicates both global and local efficiency at minimal wiring costs, and also modular organization, which indicates functional segregation and specialization. However, the important questions of how and when the small-world topology and modular organization come into existence remain largely unanswered. Taking a graph theoretic approach, we attempt to shed light on this matter by an in vivo study, using diffusion tensor imaging based fiber tractography, on 39 healthy pediatric subjects with longitudinal data collected at average ages of 2 weeks, 1 year, and 2 years. Our results indicate that the small-world architecture exists at birth with efficiency that increases in later stages of development. In addition, we found that the networks are broad scale in nature, signifying the existence of pivotal connection hubs and resilience of the brain network to random and targeted attacks. We also observed, with development, that the brain network seems to evolve progressively from a local, predominantly proximity based, connectivity pattern to a more distributed, predominantly functional based, connectivity pattern. These observations suggest that the brain in the early years of life has relatively efficient systems that may solve similar information processing problems, but in divergent ways
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