5,614 research outputs found

    A clean signal for a top-like isosinglet fermion at the Large Hadron Collider

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    We predict a clean signal at the Large Hadron Collider (s)\sqrt s)=14 TeV for a scenario where there is a top-like, charge +2/3 vectorlike isosinglet fermion. Such a quark, via mixing with the standard model top, can undergo decays via both flavour-changing Z-boson coupling and flavour-changing Yukawa interactions. We concentrate on the latter channel, and study the situation where, following its pair-production, the heavy quark pair gives rise to two tops and two Higgs boson. We show that the case where each Higgs decays in the bbˉb\bar{b} channel, there can be a rather distinct and background-free signal that can unveil the existence of the vectorlike isosinglet quark of this kind.Comment: 14 pages, 5 figures, 4 table

    Triboson interpretations of the ATLAS diboson excess

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    The ATLAS excess in fat jet pair production is kinematically compatible with the decay of a heavy resonance into two gauge bosons plus an extra particle. This hypothesis would explain the absence of such a large excess in the analogous CMS analysis of fat dijet final states, as well as the negative results of diboson resonance searches in the semi-leptonic decay modes. If the extra particle is the Higgs boson, this hypothesis might also explain -statistical fluctuations aside- why the CMS search for WH resonances in the semi-leptonic channel finds some excess while in the fully hadronic one it does not have a significant deviation.Comment: LaTeX 17 pages. v2: Enlarged discussion to address CMS WH excess. v3: Added discussion of diboson helicities. Final version to appear in JHE

    Dilepton azimuthal correlations in tt production

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    The dilepton azimuthal correlation, namely the difference phi between the azimuthal angles of the positive and negative charged lepton in the laboratory frame, provides a stringent test of the spin correlation in tt production at the Large Hadron Collider. We introduce a parameterisation of the differential cross section dalpha=dphi in terms of a Fourier series and show that the third-order expansion provides a su ciently accurate approximation. This expansion can be considered as a `bridge' between theory and data, making it very simple to cast predictions in the Standard Model (SM) and beyond, and to report measurements, without the need to provide the numbers for the whole binned distribution. We show its application by giving predictions for the coeffcients in the presence of (i) an anomalous top chromomagnetic dipole moment; (ii) an anomalous tbW interaction. The methods presented greatly facilitate the study of this angular distribution, which is of special interest given the 3:2(3:7) deviation from the SM next-to-leading order prediction found by the ATLAS collaboration in Run 2 data.This work has been supported by MINECO Project FPA 2013-47836-C3-2-P (including ERDF)

    EFTfitter: A tool for interpreting measurements in the context of effective field theories

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    Over the past years, the interpretation of measurements in the context of effective field theories has attracted much attention in the field of particle physics. We present a tool for interpreting sets of measurements in such models using a Bayesian ansatz by calculating the posterior probabilities of the corresponding free parameters numerically. An example is given, in which top-quark measurements are used to constrain anomalous couplings at the Wtb-vertex.The authors would like to thank Fabian Bach, Kathrin Becker, Dominic HirschbĂĽhl and Mikolaj Misiak for their help and for the fruitful discussions. In particular, the authors would like to thank Fabian Bach for providing the code for the single-top cross sections. N.C. acknowledges the support of FCT-Portugal through the contract IF/00050/2013/CP1172/CT00

    ifCNV: A novel isolation-forest-based package to detect copy-number variations from various targeted NGS datasets

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    Copy-number variations (CNVs) are an essential component of genetic variation distributed across large parts of the human genome. CNV detection from next-generation sequencing data and artificial intelligence algorithms have progressed in recent years. However, only a few tools have taken advantage of machine-learning algorithms for CNV detection, and none propose using artificial intelligence to automatically detect probable CNV-positive samples. The most developed approach is to use a reference or normal dataset to compare with the samples of interest, and it is well known that selecting appropriate normal samples represents a challenging task that dramatically influences the precision of results in all CNV-detecting tools. With careful consideration of these issues, we propose here ifCNV, a new software based on isolation forests that creates its own reference, available in R and python with customizable parameters. ifCNV combines artificial intelligence using two isolation forests and a comprehensive scoring method to faithfully detect CNVs among various samples. It was validated using targeted next-generation sequencing (NGS) datasets from diverse origins (capture and amplicon, germline and somatic), and it exhibits high sensitivity, specificity, and accuracy. ifCNV is a publicly available open-source software (https://github.com/SimCab-CHU/ifCNV) that allows the detection of CNVs in many clinical situations
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