632 research outputs found

    On binary reflected Gray codes and functions

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    AbstractThe binary reflected Gray code function b is defined as follows: If m is a nonnegative integer, then b(m) is the integer obtained when initial zeros are omitted from the binary reflected Gray code of m.This paper examines this Gray code function and its inverse and gives simple algorithms to generate both. It also simplifies Conder's result that the jth letter of the kth word of the binary reflected Gray code of length n is 2n-2n-j-1⌊2n-2n-j-1-k/2⌋mod2by replacing the binomial coefficient by k-12n-j+1+12

    Torsion in Buildings Subjected to Earthquakes

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    https://deepblue.lib.umich.edu/bitstream/2027.42/154131/1/39015094008060.pd

    Torsion in Buildings Subjected to Earthquakes

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    National Science Foundationhttp://deepblue.lib.umich.edu/bitstream/2027.42/116059/1/39015094008060.pd

    Evaluation of clinical prediction models (part 2):how to undertake an external validation study

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    External validation studies are an important but often neglected part of prediction model research. In this article, the second in a series on model evaluation, Riley and colleagues explain what an external validation study entails and describe the key steps involved, from establishing a high quality dataset to evaluating a model’s predictive performance and clinical usefulness.</p

    Planar selective Leidenfrost propulsion without physically structured substrates or walls

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    The Leidenfrost effect allows droplets to be transported on a virtually frictionless layer of vapor above a superheated substrate. The substrates are normally topographically structured using subtractive techniques to produce saw-tooth, herringbone, and other patterns and bulk heated, leading to significant challenges in energy consumption and controlled operation. Here, we propose a planar lithographic approach to levitate and propel droplets using temperature profiles, which can be spatially patterned and controlled in time. We show that micro-patterned electrodes can be heated and provide control of the pressure profile and the vapor flow. Using these almost featureless planar substrates, we achieve self-directed motion of droplets, with velocities of approximately 30 mms−1, without topographically structuring the substrate or introducing physical walls. Our approach has the potential to be integrated into applications, such as digital microfluidics, where frictionless and contactless droplet transport may be advantageous

    A description of the origins, design and performance of the TRAITS-SGP Atlantic salmon Salmo salar L. cDNA microarray

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    The origins, design, fabrication and performance of an Atlantic salmon microarray are described. The microarray comprises 16 950 Atlantic salmon-derived cDNA features, printed in duplicate and mostly sourced from pre-existing expressed sequence tag (EST) collections [SALGENE and salmon genome project (SGP)] but also supplemented with cDNAs from suppression subtractive hybridization libraries and candidate genes involved in immune response, protein catabolism, lipid metabolism and the parr–smolt transformation. A preliminary analysis of a dietary lipid experiment identified a number of genes known to be involved in lipid metabolism. Significant fold change differences (as low as 1.2x) were apparent from the microarray analysis and were confirmed by quantitative real-time polymerase chain reaction analysis. The study also highlighted the potential for obtaining artefactual expression patterns as a result of cross-hybridization of similar transcripts. Examination of the robustness and sensitivity of the experimental design employed demonstrated the greater importance of biological replication over technical (dye flip) replication for identification of a limited number of key genes in the studied system. The TRAITS (TRanscriptome Analysis of Important Traits of Salmon)–salmon genome project microarray has been proven, in a number of studies, to be a powerful tool for the study of key traits of Atlantic salmon biology. It is now available for use by researchers in the wider scientific community

    Evaluation of clinical prediction models (part 1):from development to external validation

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    Evaluating the performance of a clinical prediction model is crucial to establish its predictive accuracy in the populations and settings intended for use. In this article, the first in a three part series, Collins and colleagues describe the importance of a meaningful evaluation using internal, internal-external, and external validation, as well as exploring heterogeneity, fairness, and generalisability in model performance

    Antagonism of ␦ 2 -Opioid Receptors by Naltrindole-5Ј- isothiocyanate Attenuates Heroin Self-Administration but Not Antinociception in Rats 1

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    ABSTRACT ␦-Opioid receptors have been implicated in reinforcement processes and antagonists are available that produce long-lasting and selective antagonism of ␦-opioid receptors in vivo. This experiment assessed the contribution of ␦-opioid receptors to the antinociceptive and reinforcing properties of heroin. The effects of the irreversible ␦-antagonist naltrindole-5Ј-isothiocyanate (5Ј-NTII) were evaluated on heroin self-administration and hot-plate antinociception in rats. 5Ј-NTII (10 nmol i.c.v.) shifted the dose-response curve for heroin self-administration downward, increasing the A 50 values on the ascending and descending limbs by approximately 0.5 log units and decreasing the maximum by 33%. 5Ј-NTII (40 nmol i.c.v.) shifted both limbs of the heroin self-administration dose-effect curve 1.2 log units to the right and decreased the maximum by 90%. Heroin self-administration gradually returned to baseline levels over 7 or 17 days after administration of 10 or 40 nmol 5Ј-NTII, respectively. 5Ј-NTII (40 nmol i.c.v.) decreased the self-administration of 0.17 mg/infusion cocaine by 40% while having no effect on responding maintained by 0.33 or 0.67 mg/infusion. 5Ј-NTII attenuated the antinociceptive effects of deltorphin (␦ 2 ) in a dose-dependent manner while having no effect on antinociception elicited after i

    Present and Future CP Measurements

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    We review theoretical and experimental results on CP violation summarizing the discussions in the working group on CP violation at the UK phenomenology workshop 2000 in Durham.Comment: 104 pages, Latex, to appear in Journal of Physics

    Investigating Childhood Leukemia in Churchill County, Nevada

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    BACKGROUND: Sixteen children diagnosed with acute leukemia between 1997 and 2002 lived in Churchill County, Nevada, at the time of or before their illness. Considering the county population and statewide cancer rate, fewer than two cases would be expected. OBJECTIVES: In March 2001, the Centers for Disease Control and Prevention led federal, state, and local agencies in a cross-sectional, case-comparison study to determine if ongoing environmental exposures posed a health risk to residents and to compare levels of contaminants in environmental and biologic samples collected from participating families. METHODS: Surveys with more than 500 variables were administered to 205 people in 69 families. Blood, urine, and cheek cell samples were collected and analyzed for 139 chemicals, eight viral markers, and several genetic polymorphisms. Air, water, soil, and dust samples were collected from almost 80 homes to measure more than 200 chemicals. RESULTS: The scope of this cancer cluster investigation exceeded any previous study of pediatric leukemia. Nonetheless, no exposure consistent with leukemia risk was identified. Overall, tungsten and arsenic levels in urine and water samples were significantly higher than national comparison values; however, levels were similar among case and comparison groups. CONCLUSIONS: Although the cases in this cancer cluster may in fact have a common etiology, their small number and the length of time between diagnosis and our exposure assessment lessen the ability to find an association between leukemia and environmental exposures. Given the limitations of individual cancer cluster investigations, it may prove more efficient to pool laboratory and questionnaire data from similar leukemia clusters
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