Projektbeschreibung
Modellierung der Elektrophysiologie des Herzens
Herzrhythmusstörungen – also ein unregelmäßiger Herzschlag – sind häufige Ursachen für Tod und Invalidität. Zur Erforschung der diesen Arrhythmien zugrunde liegenden komplexen Elektrik werden meist mathematische Modelle angewendet. Die Forschungsgruppe des EU-finanzierten Projekts MICROCARD möchte einen Nachfolger dieser Modelle der Elektrophysiologie des Herzens erarbeiten, der die einzelnen Zellen und deren Verbindungen abbildet. Dies erhöht jedoch die Größe und Komplexität der Simulation erheblich und erfordert Hochleistungsrechnen im Exa-Maßstab. Daher wird im Rahmen von MICROCARD eine leistungsfähige Simulationsplattform entwickelt, die für Exa-Rechner geeignet ist und belastbare Erkenntnisse über die Elektrophysiologie des Herzens und ähnlicher biologischer Systeme wie Nerven, Muskeln, das Auge und das Gehirn liefert.
Ziel
Cardiovascular diseases are the most frequent cause of death worldwide and half of these deaths are due to cardiac arrhythmia, a disorder of the heart's electrical synchronization system. Numerical models of this complex system are highly sophisticated and widely used, but to match observations in aging and diseased hearts they need to move from a continuum approach to a representation of individual cells and their interconnections. This implies a different, harder numerical problem and a 10,000-fold increase in problem size. Exascale computers will be needed to run such models.
We propose to develop an exascale application platform for cardiac electrophysiology simulations that is usable for cell-by-cell simulations. The platform will be co-designed by HPC experts, numerical scientists, biomedical engineers, and biomedical scientists, from academia and industry. We will develop, in concert, numerical schemes suitable for exascale parallelism, problem-tailored linear-system solvers and preconditioners, and a compiler to translate high-level model descriptions into optimized, energy-efficient system code for heterogeneous computing systems. The code will be parallelized with a recently developed runtime system that is resilient to hardware failures and will use an energy-aware task placement strategy.
The platform will be applied in real-life use cases with high impact in the biomedical domain and will showcase HPC in this area where it is painfully underused. It will be made accessible for a wide range of users both as code and through a web interface.
We will further employ our HPC and biomedical expertise to accelerate the development of parallel segmentation and (re)meshing software, necessary to create the extremely large and complex meshes needed from available large volumes of microscopy data.
The platform will be adaptable to similar biological systems such as nerves, and components of the platform will be reusable in a wide range of applications.
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IA - Innovation actionKoordinator
33000 Bordeaux
Frankreich