984 research outputs found
Improving distributed runoff prediction in urbanized catchments with remote sensing based estimates of impervious surface cover
The amount and intensity of runoff on catchment scale are strongly determined by the presence of impervious land-cover types, which are the predominant cover types in urbanized areas. This paper examines the impact of different methods for estimating impervious surface cover on the prediction of peak discharges, as determined by a fully distributed rainfall-runoff model (WetSpa), for the upper part of the Woluwe River catchment in the southeastern part of Brussels. The study shows that detailed information on the spatial distribution of impervious surfaces, as obtained from remotely sensed data, produces substantially different estimates of peak discharges than traditional approaches based on expert judgment of average imperviousness for different types of urban land use. The study also demonstrates that sub-pixel estimation of imperviousness may be a useful alternative for more expensive high-resolution mapping for rainfall-runoff modelling at catchment scale
Recommendations of the LHC Dark Matter Working Group: Comparing LHC searches for heavy mediators of dark matter production in visible and invisible decay channels
Weakly-coupled TeV-scale particles may mediate the interactions between
normal matter and dark matter. If so, the LHC would produce dark matter through
these mediators, leading to the familiar "mono-X" search signatures, but the
mediators would also produce signals without missing momentum via the same
vertices involved in their production. This document from the LHC Dark Matter
Working Group suggests how to compare searches for these two types of signals
in case of vector and axial-vector mediators, based on a workshop that took
place on September 19/20, 2016 and subsequent discussions. These suggestions
include how to extend the spin-1 mediated simplified models already in
widespread use to include lepton couplings. This document also provides
analytic calculations of the relic density in the simplified models and reports
an issue that arose when ATLAS and CMS first began to use preliminary numerical
calculations of the dark matter relic density in these models.Comment: 19 pages, 4 figures; v2: author list and LaTeX problem fixe
Full Hierarchic Versus Non-Hierarchic Classification Approaches for Mapping Sealed Surfaces at the Rural-Urban Fringe Using High-Resolution Satellite Data
Since 2008 more than half of the world population is living in cities and urban sprawl is continuing. Because of these developments, the mapping and monitoring of urban environments and their surroundings is becoming increasingly important. In this study two object-oriented approaches for high-resolution mapping of sealed surfaces are compared: a standard non-hierarchic approach and a full hierarchic approach using both multi-layer perceptrons and decision trees as learning algorithms. Both methods outperform the standard nearest neighbour classifier, which is used as a benchmark scenario. For the multi-layer perceptron approach, applying a hierarchic classification strategy substantially increases the accuracy of the classification. For the decision tree approach a one-against-all hierarchic classification strategy does not lead to an improvement of classification accuracy compared to the standard all-against-all approach. Best results are obtained with the hierarchic multi-layer perceptron classification strategy, producing a kappa value of 0.77. A simple shadow reclassification procedure based on characteristics of neighbouring objects further increases the kappa value to 0.84
Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability
Emerging evidence suggested a converging mechanism in neurodegenerative brain diseases (NBD) involving early neuronal network dysfunctions and alterations in the homeostasis of neuronal firing as culprits of neurodegeneration. In this study, we used paired-end short-read and direct long-read whole genome sequencing to investigate an unresolved autosomal dominant dementia family significantly linked to 7q36. We identified and validated a chromosomal inversion of ca. 4Mb, segregating on the disease haplotype and disrupting the coding sequence of dipeptidyl-peptidase 6 gene (DPP6). DPP6 resequencing identified significantly more rare variants-nonsense, frame-shift, and missense-in early-onset Alzheimer's disease (EOAD, p value = 0.03, OR = 2.21 95% CI 1.05-4.82) and frontotemporal dementia (FTD, p = 0.006, OR = 2.59, 95% CI 1.28-5.49) patient cohorts. DPP6 is a type II transmembrane protein with a highly structured extracellular domain and is mainly expressed in brain, where it binds to the potassium channel K(v)4.2 enhancing its expression, regulating its gating properties and controlling the dendritic excitability of hippocampal neurons. Using in vitro modeling, we showed that the missense variants found in patients destabilize DPP6 and reduce its membrane expression (p < 0.001 and p < 0.0001) leading to a loss of protein. Reduced DPP6 and/or K(v)4.2 expression was also detected in brain tissue of missense variant carriers. Loss of DPP6 is known to cause neuronal hyperexcitability and behavioral alterations in Dpp6-KO mice. Taken together, the results of our genomic, genetic, expression and modeling analyses, provided direct evidence supporting the involvement of DPP6 loss in dementia. We propose that loss of function variants have a higher penetrance and disease impact, whereas the missense variants have a variable risk contribution to disease that can vary from high to low penetrance. Our findings of DPP6, as novel gene in dementia, strengthen the involvement of neuronal hyperexcitability and alteration in the homeostasis of neuronal firing as a disease mechanism to further investigate
Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traits
INTRODUCTION: Despite increasing evidence of a role of rare genetic variation in the risk of Alzheimer's disease (AD), limited attention has been paid to its contribution to AD-related biomarker traits indicative of AD-relevant pathophysiological processes. METHODS: We performed whole-exome gene-based rare-variant association studies (RVASs) of 17 AD-related traits on whole-exome sequencing (WES) data generated in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery (EMIF-AD MBD) study (n = 450) and whole-genome sequencing (WGS) data from ADNI (n = 808). RESULTS: Mutation screening revealed a novel probably pathogenic mutation (PSEN1 p.Leu232Phe). Gene-based RVAS revealed the exome-wide significant contribution of rare coding variation in RBKS and OR7A10 to cognitive performance and protection against left hippocampal atrophy, respectively. DISCUSSION: The identification of these novel gene-trait associations offers new perspectives into the role of rare coding variation in the distinct pathophysiological processes culminating in AD, which may lead to identification of novel therapeutic and diagnostic targets
Physics searches at the LHC
With the LHC up and running, the focus of experimental and theoretical high
energy physics will soon turn to an interpretation of LHC data in terms of the
physics of electroweak symmetry breaking and the TeV scale. We present here a
broad review of models for new TeV-scale physics and their LHC signatures. In
addition, we discuss possible new physics signatures and describe how they can
be linked to specific models of physics beyond the Standard Model. Finally, we
illustrate how the LHC era could culminate in a detailed understanding of the
underlying principles of TeV-scale physics.Comment: 184 pages, 55 figures, 14 tables, hundreds of references; scientific
feedback is welcome and encouraged. v2: text, references and Overview Table
added; feedback still welcom
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability
Emerging evidence suggested a converging mechanism in neurodegenerative brain diseases (NBD) involving early neuronal
network dysfunctions and alterations in the homeostasis of neuronal fring as culprits of neurodegeneration. In this study,
we used paired-end short-read and direct long-read whole genome sequencing to investigate an unresolved autosomal
dominant dementia family signifcantly linked to 7q36. We identifed and validated a chromosomal inversion of ca. 4 Mb,
segregating on the disease haplotype and disrupting the coding sequence of dipeptidyl-peptidase 6 gene (DPP6). DPP6
resequencing identifed signifcantly more rare variants—nonsense, frameshift, and missense—in early-onset Alzheimer’s
disease (EOAD, p value=0.03, OR=2.21 95% CI 1.05–4.82) and frontotemporal dementia (FTD, p=0.006, OR=2.59, 95%
CI 1.28–5.49) patient cohorts. DPP6 is a type II transmembrane protein with a highly structured extracellular domain and
is mainly expressed in brain, where it binds to the potassium channel Kv4.2 enhancing its expression, regulating its gating
properties and controlling the dendritic excitability of hippocampal neurons. Using in vitro modeling, we showed that the
missense variants found in patients destabilize DPP6 and reduce its membrane expression (p<0.001 and p<0.0001) leading
to a loss of protein. Reduced DPP6 and/or Kv4.2 expression was also detected in brain tissue of missense variant carriers.
Loss of DPP6 is known to caus
A Roadmap for HEP Software and Computing R&D for the 2020s
Particle physics has an ambitious and broad experimental programme for the coming decades. This programme requires large investments in detector hardware, either to build new facilities and experiments, or to upgrade existing ones. Similarly, it requires commensurate investment in the R&D of software to acquire, manage, process, and analyse the shear amounts of data to be recorded. In planning for the HL-LHC in particular, it is critical that all of the collaborating stakeholders agree on the software goals and priorities, and that the efforts complement each other. In this spirit, this white paper describes the R&D activities required to prepare for this software upgrade.Peer reviewe
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