SCI Publications
2012
T. Liu, E. Jurrus, M. Seyedhosseini, M. Ellisman, T. Tasdizen.
Watershed Merge Tree Classification for Electron Microscopy Image Segmentation, In Proceedings of the 21st International Conference on Pattern Recognition (ICPR), pp. 133--137. 2012.
S. Liu, J.A. Levine, P.-T. Bremer, V. Pascucci.
Gaussian Mixture Model Based Volume Visualization, In Proceedings of the IEEE Large-Scale Data Analysis and Visualization Symposium 2012, Note: Received Best Paper Award, pp. 73--77. 2012.
DOI: 10.1109/LDAV.2012.6378978
Keywords: Uncertainty Visualization, Volume Rendering, Gaussian Mixture Model, Ensemble Visualization
W. Liu, S. Awate, P.T. Fletcher.
Group Analysis of Resting-State fMRI by Hierarchical Markov Random Fields, In Medical Image Computing and Computer-Assisted Intervention – MICCAI 2012, Lecture Notes in Computer Science (LNCS), Vol. 7512, pp. 189--196. 2012.
ISBN: 978-3-642-33453-5
DOI: 10.1007/978-3-642-33454-2_24
Y. Livnat, T.-M. Rhyne, M. Samore.
Epinome: A Visual-Analytics Workbench for Epidemiology Data, In IEEE Computer Graphics and Applications, Vol. 32, No. 2, pp. 89--95. 2012.
ISSN: 0272-1716
DOI: 10.1109/MCG.2012.31
Effective detection of and response to infectious disease outbreaks depend on the ability to capture and analyze information and on how public health officials respond to this information. Researchers have developed various surveillance systems to automate data collection, analysis, and alert generation, yet the massive amount of collected data often leads to information overload. To improve decision-making in outbreak detection and response, it's important to understand how outbreak investigators seek relevant information. Studying their information-search strategies can provide insight into their cognitive biases and heuristics. Identifying the presence of such biases will enable the development of tools that counter balance them and help users develop alternative scenarios.
We implemented a large-scale high-fidelity simulation of scripted infectious-disease outbreaks to help us study public health practitioners' information- search strategies. We also developed Epinome, an integrated visual-analytics investigation system. Epinome caters to users' needs by providing a variety of investigation tools. It facilitates user studies by recording which tools they used, when, and how. (See the video demonstration of Epinome at www.sci.utah.edu/gallery2/v/ software/epinome.) Epinome provides a dynamic environment that seamlessly evolves and adapts to user tasks and needs. It introduces four userinteraction paradigms in public health:
• an evolving visual display,
• seamless integration between disparate views,
• loosely coordinated multiple views, and
• direct interaction with data items.
Using Epinome, users can replay simulation scenarios, investigate an unfolding outbreak using a variety of visualization tools, and steer the simulation by implementing different public health policies at predefined decision points. Epinome records user actions, such as tool selection, interactions with each tool, and policy changes, and stores them in a database for postanalysis. A psychology team can then use that information to study users' search strategies.
H. Lu, M. Berzins, C.E. Goodyer, P.K. Jimack.
Adaptive High-Order Discontinuous Galerkin Solution of Elastohydrodynamic Lubrication Point Contact Problems, In Advances in Engineering Software, Vol. 45, No. 1, pp. 313--324. 2012.
DOI: 10.1016/j.advengsoft.2011.10.006
Keywords: Elastohydrodynamic lubrication, Discontinuous Galerkin, High polynomial degree, h-adaptivity, Nonlinear systems
A.E. Lyall, S. Woolson, H.M. Wolf, B.D. Goldman, J.S. Reznick, R.M. Hamer, W. Lin, M. Styner, G. Gerig, J.H. Gilmore.
Prenatal isolated mild ventriculomegaly is associated with persistent ventricle enlargement at ages 1 and 2, In Early Human Development, Elsevier, pp. (in press). 2012.
Background: Enlargement of the lateral ventricles is thought to originate from abnormal prenatal brain development and is associated with neurodevelopmental disorders. Fetal isolated mild ventriculomegaly (MVM) is associated with the enlargement of lateral ventricle volumes in the neonatal period and developmental delays in early childhood. However, little is known about postnatal brain development in these children.
Methods: Twenty-eight children with fetal isolated MVM and 56 matched controls were followed at ages 1 and 2 years with structural imaging on a 3T Siemens scanner and assessment of cognitive development with the Mullen Scales of Early Learning. Lateral ventricle, total gray and white matter volumes, and Mullen cognitive composite scores and subscale scores were compared between groups.
Results: Compared to controls, children with prenatal isolated MVM had significantly larger lateral ventricle volumes at ages 1 and 2 years. Lateral ventricle volume at 1 and 2 years of age was significantly correlated with prenatal ventricle size. Enlargement of the lateral ventricles was associated with increased intracranial volumes and increased gray and white matter volumes. Children with MVM had Mullen composite scores similar to controls, although there was evidence of delay in fine motor and expressive language skills.
Conclusions: Children with prenatal MVM have persistent enlargement of the lateral ventricles through the age of 2 years; this enlargement is associated with increased gray and white matter volumes and some evidence of delay in fine motor and expressive language development. Further study is needed to determine if enlarged lateral ventricles are associated with increased risk for neurodevelopmental disorders.
S.A. Maas, B.J. Ellis, G.A. Ateshian, J.A. Weiss.
FEBio: Finite elements for biomechanics, In Journal of Biomechanical Engineering, Vol. 134, No. 1, pp. 011005. 2012.
DOI: 10.1115/1.4005694
PubMed ID: 22482660
T. Martin, G. Chen, S. Musuvathy, E. Cohen, C.D. Hansen.
Generalized Swept Mid-structure for Polygonal Models, In Computer Graphics Forum, Vol. 31, No. 2 part 4, Wiley-Blackwell, pp. 805--814. May, 2012.
DOI: 10.1111/j.1467-8659.2012.03061.x
Keywords: scidac, kaust
K.S. McDowell, F. Vadakkumpadan, R. Blake, J. Blauer, G. Plank, R.S. MacLeod, N.A. Trayanova.
Methodology for patient-specific modeling of atrial fibrosis as a substrate for atrial fibrillation, In Journal of Electrocardiology, Vol. 45, No. 6, pp. 640--645. 2012.
DOI: 10.1016/j.jelectrocard.2012.08.005
PubMed ID: 22999492
PubMed Central ID: PMC3515859
Keywords: Patient-specific modeling, Computational model, Atrial fibrillation, Atrial fibrosis
Q. Meng, M. Berzins.
Scalable Large-scale Fluid-structure Interaction Solvers in the Uintah Framework via Hybrid Task-based Parallelism Algorithms, SCI Technical Report, No. UUSCI-2012-004, SCI Institute, University of Utah, 2012.
Keywords: uintah, csafe
Q. Meng, A. Humphrey, M. Berzins.
The Uintah Framework: A Unified Heterogeneous Task Scheduling and Runtime System, In Digital Proceedings of The International Conference for High Performance Computing, Networking, Storage and Analysis, Note: SC’12 –2nd International Workshop on Domain-Specific Languages and High-Level Frameworks for High Performance Computing, WOLFHPC 2012, pp. 2441--2448. 2012.
DOI: 10.1109/SCC.2012.6674233
The development of a new unified, multi-threaded runtime system for the execution of asynchronous tasks on heterogeneous systems is described in this work. These asynchronous tasks arise from the Uintah framework, which was developed to provide an environment for solving a broad class of fluid-structure interaction problems on structured adaptive grids. Uintah has a clear separation between its MPI-free user-coded tasks and its runtime system that ensures these tasks execute efficiently. This separation also allows for complete isolation of the application developer from the complexities involved with the parallelism Uintah provides. While we have designed scalable runtime systems for large CPU core counts, the emergence of heterogeneous systems, with additional on-node accelerators and co-processors presents additional design challenges in terms of effectively utilizing all computational resources on-node and managing multiple levels of parallelism. Our work addresses these challenges for Uintah by the development of new hybrid runtime system and Unified multi-threaded MPI task scheduler, enabling Uintah to fully exploit current and emerging architectures with support for asynchronous, out-of-order scheduling of both CPU and GPU computational tasks. This design coupled with an approach that uses MPI to communicate between nodes, a shared memory model on-node and the use of novel lock-free data structures, has made it possible for Uintah to achieve excellent scalability for challenging fluid-structure problems using adaptive mesh refinement on as many as 256K cores on the DoE Jaguar XK6 system. This design has also demonstrated an ability to run capability jobs on the heterogeneous systems, Keeneland and TitanDev. In this work, the evolution of Uintah and its runtime system is examined in the context of our new Unified multi-threaded scheduler design. The performance of the Unified scheduler is also tested against previous Uintah scheduler and runtime designs over a range of processor core and GPU counts.
Q. Meng, J. Hall, H. Rutigliano, X. Zhou, B.R. Sessions, R. Stott, K. Panter, C.J. Davies, R. Ranjan, D. Dosdall, R.S. MacLeod, N. Marrouche, K.L. White, Z. Wang, I.A. Polejaeva.
30 Generation of Cloned Transgenic Goats with Cardiac Specific Overexpression of Transforming Growth Factor β1, In Reproduction, Fertility and Development, Vol. 25, No. 1, pp. 162--163. 2012.
DOI: 10.1071/RDv25n1Ab30
Transforming growth factor β1 (TGF-β1) has a potent profibrotic function and is central to signaling cascades involved in interstitial fibrosis, which plays a critical role in the pathobiology of cardiomyopathy and contributes to diastolic and systolic dysfunction. In addition, fibrotic remodeling is responsible for generation of re-entry circuits that promote arrhythmias (Bujak and Frangogiannis 2007 Cardiovasc. Res. 74, 184–195). Due to the small size of the heart, functional electrophysiology of transgenic mice is problematic. Large transgenic animal models have the potential to offer insights into conduction heterogeneity associated with fibrosis and the role of fibrosis in cardiovascular diseases. The goal of this study was to generate transgenic goats overexpressing an active form of TGFβ-1 under control of the cardiac-specific α-myosin heavy chain promoter (α-MHC). A pcDNA3.1DV5-MHC-TGF-β1cys33ser vector was constructed by subcloning the MHC-TGF-β1 fragment from the plasmid pUC-BM20-MHC-TGF-β1 (Nakajima et al. 2000 Circ. Res. 86, 571–579) into the pcDNA3.1D V5 vector. The Neon transfection system was used to electroporate primary goat fetal fibroblasts. After G418 selection and PCR screening, transgenic cells were used for SCNT. Oocytes were collected by slicing ovaries from an abattoir and matured in vitro in an incubator with 5\% CO2 in air. Cumulus cells were removed at 21 to 23 h post-maturation. Oocytes were enucleated by aspirating the first polar body and nearby cytoplasm by micromanipulation in Hepes-buffered SOF medium with 10 µg of cytochalasin B mL–1. Transgenic somatic cells were individually inserted into the perivitelline space and fused with enucleated oocytes using double electrical pulses of 1.8 kV cm–1 (40 µs each). Reconstructed embryos were activated by ionomycin (5 min) and DMAP and cycloheximide (CHX) treatments. Cloned embryos were cultured in G1 medium for 12 to 60 h in vitro and then transferred into synchronized recipient females. Pregnancy was examined by ultrasonography on day 30 post-transfer. A total of 246 cloned embryos were transferred into 14 recipients that resulted in production of 7 kids. The pregnancy rate was higher in the group cultured for 12 h compared with those cultured 36 to 60 h [44.4\% (n = 9) v. 20\% (n = 5)]. The kidding rates per embryo transferred of these 2 groups were 3.8\% (n = 156) and 1.1\% (n = 90), respectively. The PCR results confirmed that all the clones were transgenic. Phenotype characterization [e.g. gene expression, electrocardiogram (ECG), and magnetic resonance imaging (MRI)] is underway. We demonstrated successful production of transgenic goat via SCNT. To our knowledge, this is the first transgenic goat model produced for cardiovascular research.
M.D. Meyer, M. Sedlmair, T. Munzner.
The Four-Level Nested Model Revisited: Blocks and Guidelines, In Workshop on BEyond time and errors: novel evaLuation methods for Information Visualization (BELIV), IEEE VisWeek 2012, 2012.
P. Muralidharan, P.T. Fletcher.
Sasaki Metrics for Analysis of Longitudinal Data on Manifolds, In Proceedings of the 2012 IEEE conference on Computer Vision and Pattern Recognition (CVPR), pp. 1027--1034. 2012.
DOI: 10.1109/CVPR.2012.6247780
Longitudinal data arises in many applications in which the goal is to understand changes in individual entities over time. In this paper, we present a method for analyzing longitudinal data that take values in a Riemannian manifold. A driving application is to characterize anatomical shape changes and to distinguish between trends in anatomy that are healthy versus those that are due to disease. We present a generative hierarchical model in which each individual is modeled by a geodesic trend, which in turn is considered as a perturbation of the mean geodesic trend for the population. Each geodesic in the model can be uniquely parameterized by a starting point and velocity, i.e., a point in the tangent bundle. Comparison between these parameters is achieved through the Sasaki metric, which provides a natural distance metric on the tangent bundle. We develop a statistical hypothesis test for differences between two groups of longitudinal data by generalizing the Hotelling T2 statistic to manifolds. We demonstrate the ability of these methods to distinguish differences in shape changes in a comparison of longitudinal corpus callosum data in subjects with dementia versus healthily aging controls.
A. Narayan, D. Xiu.
Stochastic Collocation Methods on Unstructured Grids in High Dimensions via Interpolation, In SIAM Journal on Scientific Computing, Vol. 34, No. 3, pp. A1729–-A1752. 2012.
DOI: 10.1137/110854059
Keywords: stochastic collocation, polynomial chaos, interpolation, orthogonal polynomials
A. Narayan, Y. Marzouk, D. Xiu.
Sequential Data Assimilation with Multiple Models, In Journal of Computational Physics, Vol. 231, No. 19, pp. 6401--6418. 2012.
DOI: 10.1016/j.jcp.2012.06.002
Data assimilation is an essential tool for predicting the behavior of real physical systems given approximate simulation models and limited observations. For many complex systems, there may exist several models, each with different properties and predictive capabilities. It is desirable to incorporate multiple models into the assimilation procedure in order to obtain a more accurate prediction of the physics than any model alone can provide. In this paper, we propose a framework for conducting sequential data assimilation with multiple models and sources of data. The assimilated solution is a linear combination of all model predictions and data. One notable feature is that the combination takes the most general form with matrix weights. By doing so the method can readily utilize different weights in different sections of the solution state vectors, allow the models and data to have different dimensions, and deal with the case of a singular state covariance. We prove that the proposed assimilation method, termed direct assimilation, minimizes a variational functional, a generalized version of the one used in the classical Kalman filter. We also propose an efficient iterative assimilation method that assimilates two models at a time until all models and data are assimilated. The mathematical equivalence of the iterative method and the direct method is established. Numerical examples are presented to demonstrate the effectiveness of the new method.
Keywords: Uncertainty quantification, Data assimilation, Kalman filter, Model averaging
B. Nelson, E. Liu, R.M. Kirby, R. Haimes.
ElVis: A System for the Accurate and Interactive Visualization of High-Order Finite Element Solutions, In IEEE Transactions on Visualization and Computer Graphics (TVCG), Vol. 18, No. 12, pp. 2325--2334. Dec, 2012.
DOI: 10.1109/TVCG.2012.218
A.R.C. Paiva, T. Tasdizen.
Fingerprint Image Segmentation using Data Manifold Characteristic Features, In International Journal of Pattern Recognition and Artificial Intelligence, Vol. 26, No. 4, pp. (23 pages). 2012.
DOI: 10.1142/S0218001412560101
Keywords: Fingerprint segmentation, manifold characterization, feature extraction, dimensionality reduction
B. Paniagua, L. Bompard, J. Cates, R.T. Whitaker, M. Datar, C. Vachet, M. Styner.
Combined SPHARM-PDM and entropy-based particle systems shape analysis framework, In Medical Imaging 2012: Biomedical Applications in Molecular, Structural, and Functional Imaging, SPIE Intl Soc Optical Eng, March, 2012.
DOI: 10.1117/12.911228
PubMed ID: 24027625
PubMed Central ID: PMC3766973
C Partl, A Lex, M Streit, D Kalkofen, K Kashofer, D Schmalstieg.
enRoute: Dynamic Path Extraction from Biological Pathway Maps for In-Depth Experimental Data Analysis, In Proceedings of the IEEE Symposium on Biological Data Visualization (BioVis '12), IEEE, pp. 107--114. 2012.
DOI: 10.1109/BioVis.2012.6378600
Pathway maps are an important source of information when analyzing functional implications of experimental data on biological processes. However, associating large quantities of data with nodes on a pathway map and allowing in depth-analysis at the same time is a challenging task. While a wide variety of approaches for doing so exist, they either do not scale beyond a few experiments or fail to represent the pathway appropriately. To remedy this, we introduce enRoute, a new approach for interactively exploring experimental data along paths that are dynamically extracted from pathways. By showing an extracted path side-by-side with experimental data, enRoute can present large amounts of data for every pathway node. It can visualize hundreds of samples, dozens of experimental conditions, and even multiple datasets capturing different aspects of a node at the same time. Another important property of this approach is its conceptual compatibility with arbitrary forms of pathways. Most notably, enRoute works well with pathways that are manually created, as they are available in large, public pathway databases. We demonstrate enRoute with pathways from the well-established KEGG database and expression as well as copy number datasets from humans and mice with more than 1,000 experiments. We validate enRoute using case studies with domain experts, who used enRoute to explore data for glioblastoma multiforme in humans and a model of steatohepatitis in mice.
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