Bayesian Model comparison of Higgs couplings

We investigate the possibility of contributions from physics beyond the Standard Model (SM) to the Higgs couplings, in the light of the LHC data. The work is performed within an interim framework where the magnitude of the Higgs production and decay rates are rescaled though Higgs coupling scale factors. We perform Bayesian parameter inference on these scale factors, concluding that there is good compatibility with the SM. Furthermore, we carry out Bayesian model comparison on all models where any combination of scale factors can differ from their SM values and find that typically models with fewer free couplings are strongly favoured. We consider the evidence that each coupling individually equals the SM value, making the minimal assumptions on the other couplings. Finally, we make a comparison of the SM against a single "not-SM" model, and find that there is moderate to strong evidence for the SM.Comment: 24 pages, 4 figure

A Bayesian comparison of U(1) lepton flavour models

Whether the anarchical ansatz or more symmetric structures best describe the neutrino parameters is a long standing question that underwent a revival of interest after the discovery of a non- vanishing reactor angle and the indication of a non-maximal atmospheric angle. In this letter, a Bayesian statistical approach is adopted in order to analyse and compare the two hypotheses within the context of U(1) flavour models. We study the constraints on individual model parameters and perform model comparison: the results elect constructions with built-in hierarchies among the matrix elements as preferred over the anarchical ones, with values of the evidence that depends slightly on whether the U(1) charges are also considered as free parameters or not, and on the priors used.Comment: 13 pages, 6 figure

Unparticle Self-Interactions at the Large Hadron Collider

We investigate the effect of unparticle self-interactions at the Large Hadron Collider (LHC). Especially, we discuss the three-point correlation function, which is determined by conformal symmetry up to a constant, and study its relation to processes with four-particle final states. These processes could be used as a favorable way to look for unparticle physics, and for weak enough couplings to the Standard Model, even the only way. We find updated upper bounds on the cross sections for unparticle-mediated 4 gamma final states at the LHC and novel upper bounds for the corresponding 2 gamma 2l and 4l final states. The size of the allowed cross sections obtained are comparably large for large values of the scaling dimension of the unparticle sector, but they decrease with decreasing values of this parameter. In addition, we present relevant distributions for the different final states, enabling the possible identification of the unparticle scaling dimension if there was to be a large number of events of such final states at the LHC.Comment: 29 pages, 10 figures. Final version published in Phys. Rev.

Updated determination of the solar neutrino fluxes from solar neutrino data

We present an update of the determination of the solar neutrino fluxes from a global analysis of the solar and terrestrial neutrino data in the framework of three-neutrino mixing. Using a Bayesian analysis we reconstruct the posterior probability distribution function for the eight normalization parameters of the solar neutrino fluxes plus the relevant masses and mixing, with and without imposing the luminosity constraint. We then use these results to compare the description provided by different Standard Solar Models. Our results show that, at present, both models with low and high metallicity can describe the data with equivalent statistical agreement. We also argue that even with the present experimental precision the solar neutrino data have the potential to improve the accuracy of the solar model predictions.Comment: 20 pages, 2 tables, 5 figures. arXiv admin note: substantial text overlap with arXiv:0910.458

[11C]-l-Methionine positron emission tomography in the management of children and young adults with brain tumors

Only a few Methyl-[11C]-l-methionine (MET) positron emission tomography (PET) studies have focused on children and young adults with brain neoplasm. Due to radiation exposure, long scan acquisition time, and the need for sedation in young children MET-PET studies should be restricted to this group of patients when a decision for further therapy is not possible from routine diagnostic procedures alone, e.g., structural imaging. We investigated the diagnostic accuracy of MET-PET for the differentiation between tumorous and non-tumorous lesions in this group of patients. Forty eight MET-PET scans from 39 patients aged from 2 to 21 years (mean 15 ± 5.0 years) were analyzed. The MET tumor-uptake relative to a corresponding control region was calculated. A receiver operating characteristic (ROC) was performed to determine the MET-uptake value that best distinguishes tumorous from non-tumorous brain lesions. A differentiation between tumorous (n = 39) and non-tumorous brain lesions (n = 9) was possible at a threshold of 1.48 of relative MET-uptake with a sensitivity of 83% and a specificity of 92%, respectively. A differentiation between high grade malignant lesions (mean MET-uptake = 2.00 ± 0.46) and low grade tumors (mean MET-uptake = 1.84 ± 0.31) was not possible. There was a significant difference in MET-uptake between the histologically homogeneous subgroups of astrocytoma WHO grade II and anaplastic astrocytoma WHO grade III (P = 0.02). MET-PET might be a useful tool to differentiate tumorous from non-tumorous lesions in children and young adults when a decision for further therapy is difficult or impossible from routine structural imaging procedures alone

Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

Funder: NCI U24CA211006Abstract: The Cancer Genome Atlas (TCGA) and International Cancer Genome Consortium (ICGC) curated consensus somatic mutation calls using whole exome sequencing (WES) and whole genome sequencing (WGS), respectively. Here, as part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2,658 cancers across 38 tumour types, we compare WES and WGS side-by-side from 746 TCGA samples, finding that ~80% of mutations overlap in covered exonic regions. We estimate that low variant allele fraction (VAF < 15%) and clonal heterogeneity contribute up to 68% of private WGS mutations and 71% of private WES mutations. We observe that ~30% of private WGS mutations trace to mutations identified by a single variant caller in WES consensus efforts. WGS captures both ~50% more variation in exonic regions and un-observed mutations in loci with variable GC-content. Together, our analysis highlights technological divergences between two reproducible somatic variant detection efforts