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Cacciapaglia, Giacomo,Parolini, Alberto American Physical Society 2016 Physical review. D Vol.93 No.7
<P>Vectorlike quarks, usually dubbed top partners, are a common presence in composite Higgs models. Being composite objects, their mass is expected to be of the order of their inverse size, that is the condensation scale of the new strong interactions. Light top partners, while not being a generic prediction, are, however, often considered in phenomenological models. We suggest that their lightness may be due to the matching of global't Hooft anomalies of the underlying theory. We check this mechanism in explicit models, showing that, in one case, composite fermions with the quantum numbers of the top quark obtain a mass which is controlled by a soft breaking term and can be made parametrically small.</P>
Singlets in composite Higgs models in light of the LHC 750 GeV diphoton excess
Belyaev, Alexander,Cacciapaglia, Giacomo,Cai, Haiying,Flacke, Thomas,Parolini, Alberto,Serô,dio, Hugo American Physical Society 2016 Physical review. D Vol.94 No.1
<P>Models of compositeness can successfully address the origin of the Higgs boson, as a pseudo-Nambu-Goldstone boson (pNGB) of a spontaneously broken global symmetry, and flavor physics via the partial compositeness mechanism. If the dynamics is generated by a confining gauge group with fermionic matter content, there exists only a finite set of models that have the correct properties to account for the Higgs and top partners at the same time. In this paper, we explore the theory space of this class of models; remarkably, all of them contain-beyond the pNGB Higgs-a pNGB singlet, a, which couples to Standard Model gauge bosons via Wess-Zumino-Witten interactions, thus providing naturally a resonance in the diboson at the LHC. With the assumption that the recently reported diphoton excess at 750 GeVat the LHC arises from the a resonance, we propose a generic approach on how to delineate the best candidate for composite Higgs models with top partners. We find that constraints from other diboson searches severely reduce the theory space of the models under consideration. For the models which can explain the diphoton excess, we make precise and testable predictions for the width and other diboson resonance searches.</P>
Grohs Patrick,Remaud Elodie,Lath Cybill,Vuong Kim,Parolini Marie-Lize,Dannaoui Eric,Podglajen Isabelle 대한진단검사의학회 2023 Annals of Laboratory Medicine Vol.43 No.6
Background: Matrix-assisted laser desorption ionization (MALDI) is the cornerstone of bacterial identification. The performance of a new MALDI time-of-flight mass spectrometry VITEK MS PRIME (VMS-P) system was compared with that of the MALDI Biotyper Microflex LT (MBT) system, which is routinely used in our laboratory. Methods: Sixteen bacterial and yeast reference strains cultured in 20 different media were analyzed over 10 consecutive rounds using both systems. Bacterial and yeast isolates from the routine workflow were processed using both systems. Microcolonies were identified after a 4-hour agar subculture from positive blood culture bottles, without extraction. Results: To determine the repeatability based on the reference strains, 1,190 spots were processed using each system. Correct identification was achieved for 94.0% (MBT) and 98.4% (VMS-P; P<0.01) of spots. Among these, 83.0% (MBT) and 100.0% (VMS-P) were identified with a high degree of confidence. For 1,214 spots from routine isolates, species identification was achieved for 90.0% (MBT) and 91.4% (VMS-P; P=0.26) of spots. For 69.8% (MBT) and 87.4% (VMS-P) of the spots, identification was achieved with a high degree-of-confidence score. When identification was performed using both systems, the agreement between them was 97.9%. The identification of microcolonies from positive blood culture bottles was achieved for 55.5% (MBT) and 70.2% (VMS-P; P=0.01) of spots. Conclusions: The MBT and VMS-P systems perform similarly in routine daily practice. The new VMS-P system shows high repeatability, better confidence scores for identification, and promising ability to identify microcolonies.