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Uniform tetrahedral mesh capable to help identify the internal voids of the <b>COVID-19 Main Protease. </b> Biological assembly data was retrieved from the molecule [https://www.rcsb.org/structure/6y2e 6y2e],  [https://www.rcsb.org/ Protein Data Bank].
 
Uniform tetrahedral mesh capable to help identify the internal voids of the <b>COVID-19 Main Protease. </b> Biological assembly data was retrieved from the molecule [https://www.rcsb.org/structure/6y2e 6y2e],  [https://www.rcsb.org/ Protein Data Bank].
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Uniform and graded tetrahedral meshes capable to help identify the internal voids of the <b>COVID-19 spike glycoprotein. </b> The middle and right meshes are slices. Biological assembly data was retrieved from the molecule [https://www.rcsb.org/structure/6vxx 6vxx],  [https://www.rcsb.org/ Protein Data Bank].
 
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Uniform and graded tetrahedral meshes capable to help identify the internal voids of the <b>COVID-19 spike glycoprotein. </b> The middle and right meshes are slices. Biological assembly data was retrieved from the molecule [https://www.rcsb.org/structure/6vxx 6vxx][https://www.rcsb.org/ Protein Data Bank].
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Mesh generated based on the image [https://phil.cdc.gov//PHIL_Images/23354/23354.tif 23354] retrieved from the [https://www.cdc.gov/media/subtopic/images.htm Centers for Disease Control and Prevention]. For the uniform meshes, the edge-size corresponds to 15 pixels. The adaptive meshes were created by controlling the size of the elements based on the difference in the intensity of the pixels.
 
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Revision as of 06:07, 19 March 2020

Announcements

CRTC Group: Giving thanks for a productive year with such a wonderful group, very proud to share this year with all of you at CRTC (Thanks Giving 2019).

COVID-19

What we do for COVID-19 (2019-nCoV) (for more details see medical imaging examples):

Uniform tetrahedral mesh capable to help identify the internal voids of the COVID-19 spike glycoprotein. Biological assembly data was retrieved from the molecule 6vxx, Protein Data Bank.




Uniform tetrahedral mesh capable to help identify the internal voids of the COVID-19 NSP15 Endoribonuclease. Biological assembly data was retrieved from the molecule 6vww, Protein Data Bank.



Uniform tetrahedral mesh capable to help identify the internal voids of the COVID-19 Main Protease. Biological assembly data was retrieved from the molecule 6y2e, Protein Data Bank.



Uniform and graded tetrahedral meshes capable to help identify the internal voids of the COVID-19 spike glycoprotein. The middle and right meshes are slices. Biological assembly data was retrieved from the molecule 6vxx, Protein Data Bank.



Mesh generated based on the image 23354 retrieved from the Centers for Disease Control and Prevention. For the uniform meshes, the edge-size corresponds to 15 pixels. The adaptive meshes were created by controlling the size of the elements based on the difference in the intensity of the pixels.

Workshops

CNF HPC Workshop CNF Imaging Workshop
The CRTC lab in collaboration with the Jefferson lab hosted a one-day mini-workshop on Imaging and High Performance Computing (HPC). For more information see: CNF_HPC_Workshop
Logo-hpc.png
The CRTC lab in collaboration with the Jefferson lab hosted a two-day mini-workshop on Imaging and Nuclear Femptography. For more information see: CNF_Imaging_Workshop
Cnf-workshop-logo-with-letters.png

Introduction

Finite Element (FE) mesh generation is a critical component for many (bio-)engineering and science applications. CRTCLab is developing a novel framework for highly scalable and energy-efficient high-quality mesh generation for the Finite Element Analysis in three and four dimensions. CRTC effort and focus is on research activities that combine domain-and application-specific knowledge with run-time system support to improve energy efficiency and scalability of parallel FE mesh generation codes. Traditionally, parallel FE mesh generation methods and software are developed without considering the architectural features of the supercomputer platforms on which they are eventually used for production. The main reason is the complexity of sequential, and moreover parallel, mesh generation algorithms. As a result, it is too expensive, in terms of labor and time, to customize the performance of parallel mesh generation software for specific supercomputing architectures. CRTC’s basic research is funded from NSF, NASA, NRA, total $2M and target (bio-)engineering applications are: Aerospace Industry Applications and Health Care Industry Applications.

Principles for Building Practical and Scalable Domain-Specific Environment: Adaptive Data-Driven Mesh Generation for Modeling & Simulations

This graph indicates the core enabling technologies we develop at CRTC: (i) Adaptive Tessellation Techniques: Theory and Systems and the corresponding and (ii) Parallel Runtime Software Systems required to run on current and emerging Supercomputers. The pictures around indicate the five main applications we target from left to right: (a) Computational Fluid Dynamics, (b) Numerical Flow Simulations used to Predict Flow Diversion Treatment Efficacy of Cerebral Aneurysms, (c) Trauma Brain Injuries, (d) Physic Based Adaptive Deformable Registration used in Image-Guided Neurosurgery, and (e) Imaging for Nuclear Femtography with our collaborators: from NASA/LARC, Stony Brook Medical School, Navy Research Lab, Harvard Medical School, and Physics and Jefferson Lab, respectively. The common denominator for all these applications is adaptive parallel tessellation ( or known in the science and engineering community as mesh generation or image-to-mesh conversion). Parallel mesh generation is "a new research area between the boundaries of two scientific computing disciplines: computational geometry and parallel computing" [1]. The applications are listed (left to right) with respect to interactions of input form Computer-Aided Design to Sensor data like MRI, US, etc.


Broader Impact The proposed activity will have a significant and broader impact on research and education, well beyond the bounds of this specific project and its external collaborators. Other than the direct impact to parallel unstructured mesh generation and runtime systems for supercomputers like Blue Waters, this project will benefit the performance evaluation community. This project will also promote the understanding on CerebroVascular Disease (CVD, or stroke), Image Guided Surgery for Caner, and DBS for Parkisons disease, all of which are leading natural death causes in the US.

Intellectual Merit The Intellectual Merit of this project is summarized in terms of three novel contributions: (1) an understanding of the complex computation, communication, and memory utilization patterns in a telescopic superposition of multiple parallel mesh generation codes, (2) new abstractions to efficiently throttle concurrency and to implement race-to-halt execution models at multiple levels of granularity, while orchestrating intra-and inter-layer memory management, data movement, and load balancing to improve energy-efficiency of memory and interconnect components, and (3) a novel approach to leveraging off-the-shelf and state-of-the-art low core meshing codes for highly parallel simulations.

Extreme-Scale Adaptive/Anisotropic Parallel Mesh Generation

Overview

Finite Element Mesh Generation is a critical component for many (bio-) engineering and science applications. The goal of this project is to deliver a novel Telescopic framework for highly scalable and energy efficient codes. Domain-and application-specific knowledge and run-time system support are combined to improve accuracy of FE computations.

CRTCLab addresses in depth two pillars: (i) high performance computing software runtime systems and (ii) mesh generation & adaptation based on error-metrics for NASA’s Computational Fluid Dynamics (CFD) Vision 2030. Specifically, CRTC’s focus is on the following three objectives: (1) design a multi-layered algorithmic and software framework for 3D tetrahedral anisotropic parallel mesh generation using state-of-the-art functionality supported by algorithms from AFLR and CRTC’s telescopic approach for parallel mesh generation , (2) develop error-based metrics adaptive anisotropic FE mesh generation methods and (3) design a power-aware parallel runtime software system for extreme-scale adaptive CFD computations including: (i) mesh generation & adaptation, and (ii) consistent error-based metrics for adaptation of any CFD discretizations with localizable error estimates. This is a joined project with NASA/LaRC and MIT.

  • CRTC's sub-group for Extreme Scale Parallel Mesh Generation & Adaptation, from left to right: Nikos Chrisochoides, Kevin Garner, Dana Hammond (former TM from NASA/LaRC), Christos Tsolakis and Polykarpos Thomadakis.

    We have assembled a team of established leaders (see External Collaborators) that are currently developing state-of-the-art work on mesh generation and adaptivity issues relevant to NASA’s CFD 2030 Vision and will broadly impact end-user productivity of users throughout DoD and NASA.

    Objectives

    1. Design a multi-layered algorithmic and software framework for 3D tetrahedral anisotropic parallel mesh generation methods using state-of-the-art functionality supported by methods implemented in AFLR and CRTC’s telescopic approach for parallel mesh generation.
    2. Development of error-based metrics to drive an anisotropic adaptive process
    3. Design a power-aware parallel runtime software system for extreme-scale adaptive CFD computations including: (i) mesh generation & adaptation, and (ii) consistent error-based metrics for adaptation of any CFD discretization with localizable error estimates.
  • Real-time Adaptive Mesh Generation in Medical Image Computing

    This application is using adaptive (isotropic) mesh refinement to improve (in real-time in the context of image-guided neurosurgery) the accuracy of 3D Physics-Based Deformable Registration of intra-operative MRI with pre-operative MRI.

    Overview

  • Deep Brain Stimulation – CT Imaging obtained from Neurosurgical Section of SE PADRECC McGuire VAMC (with VCU)
    • Develop adaptive deformable registration method for Deep Brain Stimulation (DBS). DBS is an effective palliative therapy for patients suffering from Essential Tremor, Parkinson’s disease, and other neurological movement disorders. Modern DBS surgery makes use of stereotactic systems and image guidance to accurately place electrode leads, as well as intra-operative imaging to surveil the location of the leads and guide the surgery. The effectiveness of DBS is directly correlated with the accuracy of DBS electrode lead placement, with more accurate electrode placement leading to better clinical outcomes. This project is a joined with VCU, VA.
  • APBNRR
    • Develop a new Adaptive Physics-Based Non-Rigid Registration (APBNRR) method developed for image guided brain tumor resection. Existing evaluation indicates that the the registration accuracy and performance of APBNRR are proved sufficient to be of clinical value in the operating room. Malignant gliomas are the most common primary and metastatic brain tumors. Treatment typically includes surgical removal followed by radiotherapy or chemotherapy. Total resection is difficult to achieve during tumor removal because of the infiltrative nature of gliomas and because brain tumors are often embedded in critical functional brain tissue. In image-guided neurosurgery, co-registered pre-operative anatomical, functional, and diffusion tensor imaging can be used to facilitate a maximally safe resection of brain tumors in certain areas of the brain. However, because the brain can deform significantly during surgery, particularly in the presence of tumor resection, non-rigid registration of the preoperative image data to the patient is required. This is a joined project with Harvard Medical School, MA.
  • Images created by the I2M tool using the CBC3D Method
    • Test five new available (in the clinic) neurovascular devices that have not been compared before through angiographic washout analysis and accurate micro CT-based tessellation (i.e., mesh or grid reconstruction) and CFD analysis in idealized sidewall aneurysm models. The CFD simulations and angiographic washout analysis will be performed on flow diverter implantations in actual patient geometries. There is a need for robust and easy-to-use Image-to-Mesh (I2M) conversion methods and software that streamline the discretization of such complex vascular geometries with fine structures with the CFD modeling process. In this project we will focus on the development and validation of fully functional I2M conversion algorithms and software (i.e., tools) for complex vascular geometries with fine structures like stents. This is a joined project with Medical School at Stony Brook University, NY.