1,437 research outputs found

    The Data Quality Monitoring for the CMS Silicon Strip Tracker

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    The CMS Silicon Strip Tracker (SST), consisting of more than 10 million channels, is organized in about 15,000 detector modules and it is the largest silicon strip tracker ever built for high energy physics experiments. The Data Quality Monitoring system for the Tracker has been developed within the CMS Software framework. More than 100,000 monitorable quantities need to be managed by the DQM system that organizes them in a hierarchical structure reflecting the detector arrangement in subcomponents and the various levels of data processing. Monitorable quantities computed at the level of individual detectors are processed to extract automatic quality checks and summary results that can be visualized with specialized graphical user interfaces. In view of the great complexity of the CMS Tracker detector the standard visualization tools based on histograms have been complemented with 2 and 3 dimensional graphical images of the subdetector that can show the whole detector down to single channel resolution. The functionalities of the CMS Silicon Strip Tracker DQM system and the experience acquired during the SST commissioning will be described

    Anomalous tqγtq\gamma coupling effects in exclusive radiative B-meson decays

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    The top-quark FCNC processes will be searched for at the CERN LHC, which are correlated with the B-meson decays. In this paper, we study the effects of top-quark anomalous interactions tqγtq\gamma in the exclusive radiative BKγB\to K^*\gamma and BργB\to\rho\gamma decays. With the current experimental data of the branching ratios, the direct CP and the isospin asymmetries, bounds on the coupling κtcRγ\kappa_{tcR}^{\gamma} from BKγB\to K^*\gamma and κtuRγ\kappa_{tuR}^{\gamma} from BργB\to \rho\gamma decays are derived, respectively. The bound on κtcRγ|\kappa_{tcR}^{\gamma}| from B(BKγ){\mathcal B}(B\to K^{*}\gamma) is generally compatible with that from B(BXsγ){\mathcal B}(B\to X_{s}\gamma). However, the isospin asymmetry Δ(Kγ)\Delta(K^{*}\gamma) further restrict the phase of κtcRγ\kappa_{tcR}^{\gamma}, and the combined bound results in the upper limit, B(tcγ)<0.21\mathcal B(t\to c\gamma)<0.21%, which is lower than the CDF result. For real κtcRγ\kappa_{tcR}^{\gamma}, the upper bound on B(tcγ)\mathcal B(t\to c\gamma) is about of the same order as the 5σ5\sigma discovery potential of ATLAS with an integrated luminosity of 10fb110 {\rm fb}^{-1}. For BργB\to\rho\gamma decays, the NP contribution is enhanced by a large CKM factor Vud/Vtd|V_{ud}/V_{td}|, and the constraint on tuγtu\gamma coupling is rather restrictive, B(tuγ)<1.44×105\mathcal B(t\to u\gamma)<1.44\times 10^{-5}. With refined measurements to be available at the LHCb and the future super-B factories, we can get close correlations between BVγB\to V \gamma and the rare tqγt\to q\gamma decays, which will be studied directly at the LHC ATLAS and CMS.Comment: 25 pages, 15 figures, pdflate

    Serological epitope profile of anti-Ro52-positive patients with systemic autoimmune rheumatic diseases

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    Background: Ro52 is an interferon-inducible protein of the tripartite motif family. Antibodies against Ro52 have been described in patients with different autoimmune diseases, such as systemic lupus erythematosus and Sj\uf6gren's syndrome, that are often associated with anti-Ro60 antibodies. The Ro52 autoantigen is extraordinarily immunogenic, and its autoantibodies are directed against both linear and conformational epitopes. The aim of this study was to evaluate the prevalence of antibodies to the five Ro52 domains, as well as to Ro52 176- to 196-amino acid (aa) and 200-239-aa peptides, in different systemic autoimmune rheumatic diseases (SARDs). We also aimed to verify whether antibodies to a single domain or domain association could increase their diagnostic specificity for any SARD. Methods: Serum samples were obtained from 100 anti-Ro52 antibody-positive patients with SARDs and from 68 controls (50 healthy donors and 18 patients with other autoimmune or allergic diseases). A special line immunoassay was created containing a full-length Ro52 antigen expressed in insect cells using the baculovirus system, five recombinant Ro52 antigen fragments [Ro52-1, Ro52-2, Ro52-3, Ro52-4 (partly overlapping Ro52-1 and Ro52-2), and Ro52-5 (partly overlapping Ro52-2 and Ro52-3)], and two Ro52 peptides (176-196 aa and 200-239 aa), all expressed in Escherichia coli. Results: In patients with SARDs, fragment prevalence rates were as follows: Ro52-1 = 3 %, Ro52-2 = 97 %, Ro52-3 = 0 %, Ro52-4 = 9 %, Ro52-5 = 28 %, Ro52 175-196-aa peptide = 6 %, and Ro52 200-239-aa peptide = 74 %. All control samples were negative for the full-length Ro52 and for the five fragments tested. Conclusions: The main epitope of the Ro52 antigen was localized on fragment 2 (aa 125-267), and the majority (97 %) of SARD sera had antibodies that target this fragment. As most of the samples were positive for fragment 2 and only some for fragments 4 or 5, which partially overlap fragment 2, it seems that the target epitope is localized in the middle of fragment 2 or in the area between fragments 4 and 5. No antibody against a single epitope or a combination of epitopes was linked to any of the single SARDs

    Study of Z boson production in pPb collisions at √sNN = 5.02 TeV

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    © 2016 The Author.The production of Z bosons in pPb collisions at sNN=5.02 TeV is studied by the CMS experiment via the electron and muon decay channels. The inclusive cross section is compared to pp collision predictions, and found to scale with the number of elementary nucleon-nucleon collisions. The differential cross sections as a function of the Z boson rapidity and transverse momentum are measured. Though they are found to be consistent within uncertainty with theoretical predictions both with and without nuclear effects, the forward-backward asymmetry suggests the presence of nuclear effects at large rapidities. These results provide new data for constraining nuclear parton distribution functions
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