About this event
Bio: Amanda Randles is the Alfred Winborne Mordecai and Victoria Stover Mordecai Assistant Professor of Biomedical Sciences at Duke University. She has courtesy appointments in the departments of Mechanical Engineering and Material Science, Computer Science and Mathematics, and is a member of the Duke Cancer Institute. Amongst other recognitions, she has received the ACM Grace Murray Hopper Award, IEEE-CS Technical Consortium on High Performance Computing (TCHPC) Award, the NSF CAREER award, the NIH Director’s Early Independence Award, the LLNL Lawrence Fellowship, and the ACM/IEEE George Michael Memorial High Performance Computing Fellowship. She was also named to the World Economic Forum Young Scientist List and the MIT Technology Review World’s Top 35 Innovators under the Age of 35 list and is a Senior Member of the National Academy of Inventors. Amanda received her PhD in Applied Physics from Harvard University as a DOE Computational Graduate Fellow and NSF Fellow. Before that, she received her Master’s degree in Computer Science from Harvard University and her Bachelor’s degree in Computer Science and Physics from Duke University. Prior to graduate school, she worked as a software engineer at IBM on the Blue Gene supercomputing team. She has contributed over 70 peer-reviewed papers, 120 granted US patents, and 100 pending patent applications.
Talk Abstract: Patient-specific simulations are a promising area for personalized medicine and often times require efficient use of large-scale computational resources. In this talk, I will discuss two use cases: personalized blood flow modeling and air flow models to support ventilator splitting. In each case, I will discuss how we have developed scalable models and tuned them to represent individual patients. I will cover the acquisition of the data, building of the model, validation methods, and steps to ensure scalable and reproducible results. In terms of the blood flow models, it has been shown that hemodynamic forces can play a key role in the localization and development of disease. When combined with computational approaches that can extend the models to include physiologically accurate hematocrit levels in large regions of the circulatory system, these image-based models yield insight into the underlying mechanisms driving disease progression and inform surgical planning or the design of next generation drug delivery systems. Building a detailed, realistic model of human blood flow, however, is a formidable mathematical and computational challenge. The models must incorporate the motion of fluid, intricate geometry of the blood vessels, continual pulse-driven changes in flow and pressure, and the behavior of suspended bodies such as red blood cells. In this talk, I will discuss the development of HARVEY, a parallel fluid dynamics application designed to model hemodynamics in patient-specific geometries. I will cover the methods introduced to reduce the overall time-to-solution and enable near-linear strong scaling on some of the largest supercomputers in the world. Finally, I will present the expansion of the scope of projects to address not only vascular diseases, but also treatment planning and the movement of circulating tumor cells in the bloodstream. For the ventilator splitting work, I will discuss how we established a new model, validated it, and were able to turn around a large parameter study using 800,000 compute hours over the course of one weekend. In both cases, a problem-centric approach set the stage for building efficient models that can provide insight into patient-specific dynamics.
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