SUMMARYScalasca is a performance toolset that has been specifically designed to analyze parallel application execution behavior on large-scale systems with many thousands of processors. It offers an incremental performance-analysis procedure that integrates runtime summaries with in-depth studies of concurrent behavior via event tracing, adopting a strategy of successively refined measurement configurations. Distinctive features are its ability to identify wait states in applications with very large numbers of processes and to combine these with efficiently summarized local measurements. In this article, we review the current toolset architecture, emphasizing its scalable design and the role of the different components in transforming raw measurement data into knowledge of application execution behavior. The scalability and effectiveness of Scalasca are then surveyed from experience measuring and analyzing real-world applications on a range of computer systems.

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Many scientific and medical researchers are working towards the creation of a virtual human—a personalized digital copy of an individual—that will assist in a patient’s diagnosis, treatment and recovery. The complex nature of living systems means that the development of this remains a major challenge. We describe progress in enabling the HemeLB lattice Boltzmann code to simulate 3D macroscopic blood flow on a full human scale. Significant developments in memory management and load balancing allow near linear scaling performance of the code on hundreds of thousands of computer cores. Integral to the construction of a virtual human, we also outline the implementation of a self-coupling strategy for HemeLB. This allows simultaneous simulation of arterial and venous vascular trees based on human-specific geometries.

Drug targeting promises to substantially enhance future therapies, for example through the focussing of chemotherapeutic drugs at the site of a tumor, thus reducing the exposure of healthy tissue to unwanted damage. Promising work on the steering of medication in the human body employs magnetic fields acting on nanoparticles made of paramagnetic materials. We develop a computational tool to aid in the optimization of the physical parameters of these particles and the magnetic configuration, estimating the fraction of particles reaching a given target site in a large patient-specific vascular system for different physiological states (heart rate, cardiac output, etc.). We demonstrate the excellent computational performance of our model by its application to the simulation of paramagnetic-nanoparticle-laden flows in a circle of Willis geometry obtained from an MRI scan. The results suggest a strong dependence of the particle density at the target site on the strength of the magnetic forcing and the velocity of the background fluid flow.