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Erratum to: Search for the HH → $ b\overline{b}b\overline{b} $ process via vector-boson fusion production using proton-proton collisions at $ \sqrt{s} $ = 13 TeV with the ATLAS detector
One correction is noted for the paper. A wrong cross-section was used for the theory prediction in figure 6 due to not taking into account the VHH contamination properly in the rescaling formula for the signal samples.
Erratum: Search for new non-resonant phenomena in high-mass dilepton final states with the ATLAS detector
The Lagrangian in eq. (2.1) of JHEP 11 (2020) 005 has an erroneous factor of 1/2. The analysis code used for the results reported in the paper does not have this factor. The results remain unchanged.
Erratum to: Search for the HH → $ b\overline{b}b\overline{b} $ process via vector-boson fusion production using proton-proton collisions at $ \sqrt{s} $ = 13 TeV with the ATLAS detector
One correction is noted for the paper. A wrong cross-section was used for the theory prediction in figure 6 due to not taking into account the VHH contamination properly in the rescaling formula for the signal samples. The change in the theory prediction leads to stricter exclusion limits on the di-vector-boson–di-Higgs-boson coupling modifier κ 2V . The observed excluded region corresponds to κ 2V < –0.43 and κ 2V > 2.56, while the expected exclusion is κ 2V < –0.55 and κ 2V > 2.72. Erratum JHEP 01 (2021) 145 fixed the description in the text but contains the uncorrected figure. The correct figure is shown in the new erratum.
Measurement of Higgs boson decay into $b$-quarks in associated production with a top-quark pair in $pp$ collisions at $ \sqrt{s} $ = 13 TeV with the ATLAS detector
The associated production of a Higgs boson and a top-quark pair is measured in events characterized by the presence of one or two electrons or muons. The Higgs boson decay into a b-quark pair is used. The analyzed data, corresponding to an integrated luminosity of 139 fb –1 , were collected in proton-proton collisions at the Large Hadron Collider between 2015 and 2018 at a centre-of-mass energy of √s = 13 TeV. The measured signal strength, defined as the ratio of the measured signal yield to that predicted by the Standard Model, is $0.35$ $^{+0.36}_{–0.34}$. This result is compatible with the Standard Model prediction and corresponds to an observed (expected) significance of 1.0 (2.7) standard deviations. The signal strength is also measured differentially in bins of the Higgs boson transverse momentum in the simplified template cross-section framework, including a bin for specially selected boosted Higgs bosons with transverse momentum above 300 GeV.
Search for heavy neutral leptons in decays of W bosons produced in 13 TeV pp collisions using prompt and displaced signatures with the ATLAS detector
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Erratum to: Measurement of differential cross sections and W + /W - cross-section ratios for W boson production in association with jets at $\sqrt{s} $ = 8 TeV with the ATLAS detector
Two additions impacting tables 3 and 4 in ref. [1] are presented in the following. No significant impact is found for other results or figures in ref. [1].
Erratum to: Measurement of light-by-light scattering and search for axion-like particles with 2.2 nb -1 of Pb+Pb data with the ATLAS detector
One correction is noted for the paper, which does not affect the results reported. The right panel of figure 9 is corrected as it contained the “internal” label, giving the misleading impression on the credibility of the figure.
Atlas of Transcription Factor Binding Sites from ENCODE DNase Hypersensitivity Data across 27 Tissue Types
Characterizing the tissue-specific binding sites of transcription factors (TFs) is essential to reconstruct gene regulatory networks and predict functions for non-coding genetic variation. DNase-seq footprinting enables the prediction of genome-wide binding sites for hundreds of TFs simultaneously. Despite the public availability of high-quality DNase-seq data from hundreds of samples, a comprehensive, up-to-date resource for the locations of genomic footprints is lacking. Here, we develop a scalable footprinting workflow using two state-of-the-art algorithms: Wellington and HINT. We apply our workflow to detect footprints in 192 ENCODE DNase-seq experiments and predict the genomic occupancy of 1,515 human TFs in 27 human tissues. We validate that these footprints overlap true-positive TF binding sites from ChIP-seq. We demonstrate that the locations, depth, and tissue specificity of footprints predict effects of genetic variants on gene expression and capture a substantial proportion of genetic risk for complex traits.
Method and Atlas to Enable Targeting for Cardiac Radioablation Employing the American Heart Association Segmented Model
Cardiac radioablation using stereotactic body radiation therapy is gaining popularity as a noninvasive treatment for otherwise refractory ventricular arrhythmias. As radiation oncologists might be unaccustomed to the lexicon used by cardiologists to describe the location of arrhythmogenic foci, a preliminary guide to cardiac-specific anatomy and orientation is needed to foster effective communication between the radiation oncologist and cardiology team.
ATLAS LAr calorimeter performance in LHC run 2 and electronics upgrades for next runs
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Radiation damage from energetic particles at GRad-level of SiO 2 fibers of the Large Hadron Collider ATLAS Zero-Degree Calorimeter (ZDC)
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Effect of irradiation and annealing performed with bias voltage applied across the coupling capacitors on the interstrip resistance of ATLAS ITk silicon strip sensors
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Preliminary defect level investigation in ATLAS ITk Strip Sensors using DLTS
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Measurements of electroweak-boson-tagged jet energy loss and modification by ATLAS
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