362 research outputs found

    Further improve circuit partitioning using GBAW logic perturbation techniques

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    Four-fermion heavy quark operators and light current amplitudes in heavy flavor hadrons

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    We introduce and study the properties of the "color-straight" four-quark operators containing heavy and light quark fields. They are of the form (\bar b\Gamma_b b)(\bar q\Gamma_q q) where both brackets are color singlets. Their expectation values include the bulk of the nonfactorizable contributions to the nonleptonic decay widths of heavy hadrons. The expectation values of the color-straight operators in the heavy hadrons are related to the momentum integrals of the elastic light-quark formfactors of the respective heavy hadron. We calculate the asymptotic behavior of the light-current formfactors of heavy hadrons and show that the actual decrease is 1/(q^2)^3/2 rather than 1/q^4. The two-loop hybrid anomalous dimensions of the four-quark operators and their mixing (absent in the first loop) are obtained. Using plausible models for the elastic formfactors, we estimate the expectation values of the color-straight operators in the heavy mesons and baryons. Improved estimates will be possible in the future with new data on the radiative decays of heavy hadrons. We give the Wilson coefficients of the four-fermion operators in the 1/m_b expansion of the inclusive widths and discuss the numerical predictions. Estimates of the nonfactorizable expectation values are given.Comment: 51 pages. The case of flavor-singlet operators is added for the two-loop anomalous dimension

    Diagonalization of the neutralino mass matrix and boson-neutralino interaction

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    We analyze a connection between neutralino mass sign, parity and structure of the neutralino-boson interaction. Correct calculation of spin-dependent and spin-independent contributions to neutralino-nuclear scattering should consider this connection. A convenient diagonalization procedure, based on the exponetial parametrization of unitary matrix, is suggested.Comment: 21 pages, RevTex

    A Heavy-Light Chiral Quark Model

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    We present a new chiral quark model for mesons involving a heavy and a light (anti-) quark. The model relates various combinations of a quark - meson coupling constant and loop integrals to physical quantities. Then, some quantities may be predicted and some used as input. The extension from other similar models is that the present model includes the lowest order gluon condensate of the order (300 MeV)^4 determined by the mass splitting of the 0^- and the 1^- heavy meson states. Within the model, we find a reasonable description of parameters such as the decay constants f_B and f_D, the Isgur-Wise function and the axial vector coupling g_A in chiral perturbation theory for light and heavy mesons.Comment: 31 pages, 13 figures, RevTex4.

    Search for the radiative decay η→π0γγ\eta \to \pi^0 \gamma \gamma in the SND experiment at VEPP-2M

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    The η→π0γγ\eta \to \pi^0 \gamma \gamma decay was investigated by the SND detector at VEPP-2M e+e−e^+e^- collider in the reaction e+eâˆ’â†’Ï•â†’Î·Îłe^+e^-\to\phi\to \eta\gamma. Here we present the results and some details of this study. We report an upper limit (90% c.l.) Br(η→π0γγ)<8.4×10−4Br(\eta \to \pi^0 \gamma \gamma)<8.4\times 10^{-4} as our final result. Our upper limit does not contradict the earlier measurement by GAMS spectrometer. To facilitate future studies a rather detailed review of the problem is also given.Comment: 24 pages, 6 figures, LaTex. To be published in Nucl. Phys.

    A Bayesian analysis of pentaquark signals from CLAS data

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    We examine the results of two measurements by the CLAS collaboration, one of which claimed evidence for a Θ+\Theta^{+} pentaquark, whilst the other found no such evidence. The unique feature of these two experiments was that they were performed with the same experimental setup. Using a Bayesian analysis we find that the results of the two experiments are in fact compatible with each other, but that the first measurement did not contain sufficient information to determine unambiguously the existence of a Θ+\Theta^{+}. Further, we suggest a means by which the existence of a new candidate particle can be tested in a rigorous manner.Comment: 5 pages, 3 figure

    First measurement of direct f0(980)f_0(980) photoproduction on the proton

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    We report on the results of the first measurement of exclusive f0(980)f_0(980) meson photoproduction on protons for EÎł=3.0−3.8E_\gamma=3.0 - 3.8 GeV and −t=0.4−1.0-t = 0.4-1.0 GeV2^2. Data were collected with the CLAS detector at the Thomas Jefferson National Accelerator Facility. The resonance was detected via its decay in the π+π−\pi^+ \pi^- channel by performing a partial wave analysis of the reaction Îłp→pπ+π−\gamma p \to p \pi^+ \pi^-. Clear evidence of the f0(980)f_0(980) meson was found in the interference between PP and SS waves at Mπ+π−∌1M_{\pi^+ \pi^-}\sim 1 GeV. The SS-wave differential cross section integrated in the mass range of the f0(980)f_0(980) was found to be a factor of 50 smaller than the cross section for the ρ\rho meson. This is the first time the f0(980)f_0(980) meson has been measured in a photoproduction experiment

    An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics

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    For a decade, The Cancer Genome Atlas (TCGA) program collected clinicopathologic annotation data along with multi-platform molecular profiles of more than 11,000 human tumors across 33 different cancer types. TCGA clinical data contain key features representing the democratized nature of the data collection process. To ensure proper use of this large clinical dataset associated with genomic features, we developed a standardized dataset named the TCGA Pan-Cancer Clinical Data Resource (TCGA-CDR), which includes four major clinical outcome endpoints. In addition to detailing major challenges and statistical limitations encountered during the effort of integrating the acquired clinical data, we present a summary that includes endpoint usage recommendations for each cancer type. These TCGA-CDR findings appear to be consistent with cancer genomics studies independent of the TCGA effort and provide opportunities for investigating cancer biology using clinical correlates at an unprecedented scale. Analysis of clinicopathologic annotations for over 11,000 cancer patients in the TCGA program leads to the generation of TCGA Clinical Data Resource, which provides recommendations of clinical outcome endpoint usage for 33 cancer types
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