16 research outputs found

    Prioritized Data Compression using Wavelets

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    The volume of data and the velocity with which it is being generated by com- putational experiments on high performance computing (HPC) systems is quickly outpacing our ability to effectively store this information in its full fidelity. There- fore, it is critically important to identify and study compression methodologies that retain as much information as possible, particularly in the most salient regions of the simulation space. In this paper, we cast this in terms of a general decision-theoretic problem and discuss a wavelet-based compression strategy for its solution. We pro- vide a heuristic argument as justification and illustrate our methodology on several examples. Finally, we will discuss how our proposed methodology may be utilized in an HPC environment on large-scale computational experiments

    Alternatives to Contour Visualizations for Power Systems Data

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    Electrical grids are geographical and topological structures whose voltage states are challenging to represent accurately and efficiently for visual analysis. The current common practice is to use colored contour maps, yet these can misrepresent the data. We examine the suitability of four alternative visualization methods for depicting voltage data in a geographically dense distribution system -- Voronoi polygons, H3 tessellations, S2 tessellations, and a network-weighted contour map. We find that Voronoi tessellations and network-weighted contour maps more accurately represent the statistical distribution of the data than regular contour maps.Comment: IEEE Vis 202

    Segmentation and visualization of multivariate features using feature-local distributions

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    Abstract. We introduce an iterative feature-based transfer function design that extracts and systematically incorporates multivariate featurelocal statistics into a texture-based volume rendering process. We argue that an interactive multivariate feature-local approach is advantageous when investigating ill-defined features, because it provides a physically meaningful, quantitatively rich environment within which to examine the sensitivity of the structure properties to the identification parameters. We demonstrate the efficacy of this approach by applying it to vortical structures in Taylor-Green turbulence. Our approach identified the existence of two distinct structure populations in these data, which cannot be isolated or distinguished via traditional transfer functions based on global distributions

    African-specific alleles modify risk for asthma at the 17q12-q21 locus in African Americans

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    BACKGROUND: Asthma is the most common chronic disease in children, occurring at higher frequencies and with more severe disease in children with African ancestry. METHODS: We tested for association with haplotypes at the most replicated and significant childhood-onset asthma locus at 17q12-q21 and asthma in European American and African American children. Following this, we used whole-genome sequencing data from 1060 African American and 100 European American individuals to identify novel variants on a high-risk African American-specific haplotype. We characterized these variants in silico using gene expression and ATAC-seq data from airway epithelial cells, functional annotations from ENCODE, and promoter capture (pc)Hi-C maps in airway epithelial cells. Candidate causal variants were then assessed for correlation with asthma-associated phenotypes in African American children and adults. RESULTS: Our studies revealed nine novel African-specific common variants, enriched on a high-risk asthma haplotype, which regulated the expression of GSDMA in airway epithelial cells and were associated with features of severe asthma. Using ENCODE annotations, ATAC-seq, and pcHi-C, we narrowed the associations to two candidate causal variants that are associated with features of T2 low severe asthma. CONCLUSIONS: Previously unknown genetic variation at the 17q12-21 childhood-onset asthma locus contributes to asthma severity in individuals with African ancestries. We suggest that many other population-specific variants that have not been discovered in GWAS contribute to the genetic risk for asthma and other common diseases
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