Acceleration of cardiac tissue simulation with graphic processing units

In this technical note we show the promise of using graphic processing units (GPUs) to accelerate simulations of electrical wave propagation in cardiac tissue, one of the more demanding computational problems in cardiology. We have found that the computational speed of two-dimensional (2D) tissue simulations with a single commercially available GPU is about 30 times faster than with a single 2.0 GHz Advanced Micro Devices (AMD) Opteron processor. We have also simulated wave conduction in the three-dimensional (3D) anatomic heart with GPUs where we found the computational speed with a single GPU is 1.6 times slower than with a 32-central processing unit (CPU) Opteron cluster. However, a cluster with two or four GPUs is faster than the CPU-based cluster. These results demonstrate that a commodity personal computer is able to perform a whole heart simulation of electrical wave conduction within times that enable the investigators to interact more easily with their simulations

The Mont-Blanc prototype: an alternative approach for high-performance computing systems

High-performance computing (HPC) is recognized as one of the pillars for further advance of science, industry, medicine, and education. Current HPC systems are being developed to overcome emerging challenges in order to reach Exascale level of performance,which is expected by the year 2020. The much larger embedded and mobile market allows for rapid development of IP blocks, and provides more flexibility in designing an application-specific SoC, in turn giving possibility in balancing performance, energy-efficiency and cost. In the Mont-Blanc project, we advocate for HPC systems be built from such commodity IP blocks, currently used in embedded and mobile SoCs. As a first demonstrator of such approach, we present the Mont-Blanc prototype; the first HPC system built with commodity SoCs, memories, and NICs from the embedded and mobile domain, and off-the-shelf HPC networking, storage, cooling and integration solutions. We present the system’s architecture, and evaluation including both performance and energy efficiency. Further, we compare the system’s abilities against a production level supercomputer. At the end, we discuss parallel scalability, and estimate the maximum scalability point of this approach across a set of HPC applications.Postprint (published version

Finite element simulations: computations and applications to aerodynamics and biomedicine.

171 p.Las ecuaciones en derivadas parciales describen muchos fenómenos de interés práctico y sus solucionessuelen necesitar correr simulaciones muy costosas en clústers de cálculo.En el ámbito de los flujos turbulentos, en particular, el coste de las simulaciones es demasiado grande sise utilizan métodos básicos, por eso es necesario modelizar el sistema.Esta tesis doctoral trata principalmente de dos temas en Cálculo Científico.Por un lado, estudiamos nuevos desarrollos en la modelización y simulación de flujos turbulentos;utilizamos un Método de Elementos Finitos adaptativo y un modelo de ¿número de Reynolds infinito¿para reducir el coste computacional de simulaciones que, sin estas modificaciones, serían demasiadocostosas.De esta manera conseguimos lograr simulaciones evolutivas de flujos turbulentos con número deReynolds muy grande, lo cual se considera uno de los mayores retos en aerodinámica.El otro pilar de esta tesis es una aplicación biomédica.Desarrollamos un modelo computacional de Ablación (Cardiaca) por Radiofrecuencia, una terapiacomún para tratar varias enfermedades, por ejemplo algunas arritmias.Nuestro modelo mejora los modelos existentes en varias maneras, y en particular en tratar de obteneruna aproximación fiel de la geometría del sistema, lo cual se descubre ser crítico para simularcorrectamente la física del fenómeno

Advances in Signal and Image Processing in Biomedical Applications

Our bodies are continually passing on information about our prosperity. This information can be collected using physiological instruments that measure beat, circulatory strain, oxygen drenching levels, blood glucose, nerve conduction, mind activity, and so on. For the most part, such estimations are taken at unequivocal spotlights in time and noted on a patient’s outline. Working with conventional bio-estimation apparatuses, the sign can be figured by programming to give doctors continuous information and more noteworthy bits of knowledge to help in clinical evaluations. By utilizing progressively modern intends to break down what our bodies are stating, we can conceivably decide the condition of a patient’s wellbeing through increasingly noninvasive measures

Investigating Arrhythmia Potential in Cardiac Myocytes in Presence of Long QT Syndrome

Long QT Syndrome (LQTS) is an increasingly studied condition that leads to potentially fatal heart rhythm disorders, called arrhythmias, and sudden cardiac death. The alterations in the electrocardiograms (ECGs) seen in LQTS patients is caused by mutations to genes related to ion channels in cardiac cells. Computational modeling allows the mechanistic study of these ion channel mutations in LQTS by providing quantitative predictors of cardiac behavior in human and rabbit heart models. This work hypothesizes that the repolarization reserve in cardiac Purkinje cells (PC), that form the cardiac conduction system, is lower than that of ventricular myocytes (VM), resulting in a higher propensity of electrophysiological abnormalities in the form of spontaneous activity, particularly early and delayed afterdepolarizations (EADs and DADs, respectively). To investigate this hypothesis, detailed computational methods were created by incorporating experimental data. The computer models were then utilized to reproduce the experimentally observed behavior in single cells as well as 3-dimensional ventricular models. The computational results show more profound effects of the LQTS mutations on action potential duration (APD) prolongation in PCs when compared to VMs. Ectopic beats exist in isoproterenol conditions for human PCs. Future research includes determining the effect of these APD differences on the entirety of the heart using an anatomical 3D model of a rabbit heart