317 research outputs found

    Estimates of hadron azimuthal anisotropy from multiparton interactions in proton-proton collisions at sqrt(s) = 14 TeV

    Full text link
    We estimate the amount of collective "elliptic flow" expected at mid-rapidity in proton-proton (p-p) collisions at the CERN Large Hadron Collider (LHC), assuming that any possible azimuthal anisotropy of the produced hadrons with respect to the plane of the reaction follows the same overlap-eccentricity and particle-density scalings as found in high-energy heavy ion collisions. Using a Glauber eikonal model, we compute the p-p eccentricities, transverse areas and particle-multiplicities for various phenomenological parametrisations of the proton spatial density. For realistic proton transverse profiles, we find integrated elliptic flow v2 parameters below 3% in p-p collisions at sqrt(s) = 14 TeV.Comment: 17 pages, 9 figures. Very minor mods. Version to appear in EPJ-

    Gene set analysis exploiting the topology of a pathway

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Recently, a great effort in microarray data analysis is directed towards the study of the so-called gene sets. A gene set is defined by genes that are, somehow, functionally related. For example, genes appearing in a known biological pathway naturally define a gene set. The gene sets are usually identified from a priori biological knowledge. Nowadays, many bioinformatics resources store such kind of knowledge (see, for example, the Kyoto Encyclopedia of Genes and Genomes, among others). Although pathways maps carry important information about the structure of correlation among genes that should not be neglected, the currently available multivariate methods for gene set analysis do not fully exploit it.</p> <p>Results</p> <p>We propose a novel gene set analysis specifically designed for gene sets defined by pathways. Such analysis, based on graphical models, explicitly incorporates the dependence structure among genes highlighted by the topology of pathways. The analysis is designed to be used for overall surveillance of changes in a pathway in different experimental conditions. In fact, under different circumstances, not only the expression of the genes in a pathway, but also the strength of their relations may change. The methods resulting from the proposal allow both to test for variations in the strength of the links, and to properly account for heteroschedasticity in the usual tests for differential expression.</p> <p>Conclusions</p> <p>The use of graphical models allows a deeper look at the components of the pathway that can be tested separately and compared marginally. In this way it is possible to test single components of the pathway and highlight only those involved in its deregulation.</p

    Mid-portion Achilles tendinopathy: why painful? An evidence-based philosophy

    Get PDF
    Chronic mid-portion Achilles tendinopathy is generally difficult to treat as the background to the pain mechanisms has not yet been clarified. A wide range of conservative and surgical treatment options are available. Most address intratendinous degenerative changes when present, as it is believed that these changes are responsible for the symptoms. Since up to 34% of asymptomatic tendons show histopathological changes, we believe that the tendon proper is not the cause of pain in the majority of patients. Chronic painful tendons show the ingrowth of sensory and sympathetic nerves from the paratenon with release of nociceptive substances. Denervating the Achilles tendon by release of the paratenon is sufficient to cause pain relief in the majority of patients. This type of treatment has the additional advantage that it is associated with a shorter recovery time when compared with treatment options that address the tendon itself. An evidence-based philosophy on the cause of pain in chronic mid-portion Achilles tendinopathy is presented

    Limit On the Neutrino Magnetic Moment Using 1496 Days of Super-Kamiokande-i Solar Neutrino Data

    Full text link
    A search for a non-zero neutrino magnetic moment has been conducted using 1496 live days of solar neutrino data from {\SK}. Specifically, we searched for distortions to the energy spectrum of recoil electrons arising from magnetic scattering due to a non-zero neutrino magnetic moment. In the absence of clear signal, we found μν3.6×1010\mu_{\nu} \leq 3.6 \times 10^{-10} μB\mu_{B} at 90% C.L. by fitting to the Super-Kamiokande day/night spectra. The fitting took into account the effect of neutrino oscillation on the shapes of energy spectra. With additional information from other solar neutrino and KamLAND experiments constraining the oscillation region, a limit of μν1.1×1010\mu_{\nu} \leq 1.1 \times 10^{-10} μB\mu_{B} at 90% C.L. was obtained.Comment: 5 pages, 4 figure
    corecore