83 research outputs found

    Statistical inference for radially-stable generalized Pareto distributions and return level-sets in geometric extremes

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    We obtain a functional analogue of the quantile function for probability measures admitting a continuous Lebesgue density on Rd\mathbb{R}^d, and use it to characterize the class of non-trivial limit distributions of radially recentered and rescaled multivariate exceedances in geometric extremes. A new class of multivariate distributions is identified, termed radially stable generalized Pareto distributions, and is shown to admit certain stability properties that permit extrapolation to extremal sets along any direction in Rd\mathbb{R}^d. Based on the limit Poisson point process likelihood of the radially renormalized point process of exceedances, we develop parsimonious statistical models that exploit theoretical links between structural star-bodies and are amenable to Bayesian inference. The star-bodies determine the mean measure of the limit Poisson process through a hierarchical structure. Our framework sharpens statistical inference by suitably including additional information from the angular directions of the geometric exceedances and facilitates efficient computations in dimensions d=2d=2 and d=3d=3. Additionally, it naturally leads to the notion of the return level-set, which is a canonical quantile set expressed in terms of its average recurrence interval, and a geometric analogue of the uni-dimensional return level. We illustrate our methods with a simulation study showing superior predictive performance of probabilities of rare events, and with two case studies, one associated with river flow extremes, and the other with oceanographic extremes.Comment: 65 pages, 34 figure

    C−C Bond Formation via Double C−H Functionalization:  Aerobic Oxidative Coupling as a Method for Synthesizing Heterocoupled Biaryls

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    The aerobic oxidative coupling of arenes such as benzofuran and N-substituted indoles with benzene and derivatives thereof is described. The reaction is shown to take place in both inter- and intramolecular scenarios

    A Bayesian General Linear Modeling Approach to Cortical Surface fMRI Data Analysis

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    Cortical surface functional magnetic resonance imaging (cs-fMRI) has recently grown in popularity versus traditional volumetric fMRI. In addition to offering better whole-brain visualization, dimension reduction, removal of extraneous tissue types, and improved alignment of cortical areas across subjects, it is also more compatible with common assumptions of Bayesian spatial models. However, as no spatial Bayesian model has been proposed for cs-fMRI data, most analyses continue to employ the classical general linear model (GLM), a “massive univariate” approach. Here, we propose a spatial Bayesian GLM for cs-fMRI, which employs a class of sophisticated spatial processes to model latent activation fields. We make several advances compared with existing spatial Bayesian models for volumetric fMRI. First, we use integrated nested Laplacian approximations, a highly accurate and efficient Bayesian computation technique, rather than variational Bayes. To identify regions of activation, we utilize an excursions set method based on the joint posterior distribution of the latent fields, rather than the marginal distribution at each location. Finally, we propose the first multi-subject spatial Bayesian modeling approach, which addresses a major gap in the existing literature. The methods are very computationally advantageous and are validated through simulation studies and two task fMRI studies from the Human Connectome Project. Supplementary materials for this article, including a standardized description of the materials available for reproducing the work, are available as an online supplement

    Multicolor Photometric Observation of Lightning from Space: Comparison with Radio Measurements

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    This study evaluates the effectiveness of spectrophotometric measurements from space in revealing properties of lightning flash. The multicolor optical waveform data obtained by FORMOSAT-2/Imager of Sprites and Upper Atmospheric Lightning (ISUAL) were analyzed in relation to National Lightning Detection Network (NLDN), North Alabama Lightning Mapping Array (LMA). As of July 2011, we found six lightning events which were observed by ISUAL and North Alabama LMA. In two of these events, NLDN showed clear positive cloud-to-ground (CG) discharges with peak current of +139.9 kA and +41.6 kA and, around that time, LMA showed continuous intra-cloud (IC) leader activities at 4-6 km altitudes. ISUAL also observed consistent optical waveforms of the IC and CG components and, interestingly, it was found that the blue/red spectral ratio clearly decreased by a factor of 1.5-2.5 at the time of CG discharges. Other four lightning events in which NLDN did not detect any CG discharges were also investigated, but such a feature was not found in any of these cases. These results suggest that the optical color of CG component is more reddish than that of IC component and we explain this as a result of more effective Rayleigh scattering in blue light emissions coming from lower-altitude light source. This finding suggests that spectral measurements could be a new useful technique to characterize ICs and CGs from space. In this talk, we will also present a result from lightning statistical analysis of ISUAL spectrophotometric data and ULF magnetic data

    Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.

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    The occurrence of non-epileptic hyperkinetic movements in the context of developmental epileptic encephalopathies is an increasingly recognized phenomenon. Identification of causative mutations provides an important insight into common pathogenic mechanisms that cause both seizures and abnormal motor control. We report bi-allelic loss-of-function CACNA1B variants in six children from three unrelated families whose affected members present with a complex and progressive neurological syndrome. All affected individuals presented with epileptic encephalopathy, severe neurodevelopmental delay (often with regression), and a hyperkinetic movement disorder. Additional neurological features included postnatal microcephaly and hypotonia. Five children died in childhood or adolescence (mean age of death: 9 years), mainly as a result of secondary respiratory complications. CACNA1B encodes the pore-forming subunit of the pre-synaptic neuronal voltage-gated calcium channel Cav2.2/N-type, crucial for SNARE-mediated neurotransmission, particularly in the early postnatal period. Bi-allelic loss-of-function variants in CACNA1B are predicted to cause disruption of Ca2+ influx, leading to impaired synaptic neurotransmission. The resultant effect on neuronal function is likely to be important in the development of involuntary movements and epilepsy. Overall, our findings provide further evidence for the key role of Cav2.2 in normal human neurodevelopment.MAK is funded by an NIHR Research Professorship and receives funding from the Wellcome Trust, Great Ormond Street Children's Hospital Charity, and Rosetrees Trust. E.M. received funding from the Rosetrees Trust (CD-A53) and Great Ormond Street Hospital Children's Charity. K.G. received funding from Temple Street Foundation. A.M. is funded by Great Ormond Street Hospital, the National Institute for Health Research (NIHR), and Biomedical Research Centre. F.L.R. and D.G. are funded by Cambridge Biomedical Research Centre. K.C. and A.S.J. are funded by NIHR Bioresource for Rare Diseases. The DDD Study presents independent research commissioned by the Health Innovation Challenge Fund (grant number HICF-1009-003), a parallel funding partnership between the Wellcome Trust and the Department of Health, and the Wellcome Trust Sanger Institute (grant number WT098051). We acknowledge support from the UK Department of Health via the NIHR comprehensive Biomedical Research Centre award to Guy's and St. Thomas' National Health Service (NHS) Foundation Trust in partnership with King's College London. This research was also supported by the NIHR Great Ormond Street Hospital Biomedical Research Centre. J.H.C. is in receipt of an NIHR Senior Investigator Award. The research team acknowledges the support of the NIHR through the Comprehensive Clinical Research Network. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, Department of Health, or Wellcome Trust. E.R.M. acknowledges support from NIHR Cambridge Biomedical Research Centre, an NIHR Senior Investigator Award, and the University of Cambridge has received salary support in respect of E.R.M. from the NHS in the East of England through the Clinical Academic Reserve. I.E.S. is supported by the National Health and Medical Research Council of Australia (Program Grant and Practitioner Fellowship)

    Bayesian Generalized Two-way ANOVA Modeling for Functional Data Using INLA

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    Functional analysis of variance (ANOVA) modeling has been proved particularly useful to investigate the dynamic changes of functional data according to certain categorical factors and their interactions. The current existing methods often encounter difficulties when the functional data are high-dimensional, non-Gaussian, and/or exhibit certain shape characteristics that vary with spatial locations. In this paper, we investigate the functional two-way ANOVA models from a novel Bayesian perspective. A class of highly flexible Gaussian Markov random fields (GMRF) are taken as priors on the functions in the model, which allows us to model various types of functional effects, such as (discrete or continuous) temporal effects and (point-level or areal) spatial effects. The resulting posterior distributions are obtained by an efficient computational tool based on integrated nested Laplace approximations (INLA) Rue, Martino and Chopin (2009). We then employ the excursion method introduced by Bolin and Lindgren (2015) to build simultaneous credible intervals of functional effects and test their significance from a Bayesian point of view. A simulation study and multiple data examples are presented to demonstrate the merits of our method
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