|Authors||J. Chai, J. E. Hake, N. Wu, M. Wen, X. Cai, G. T. Lines, J. Yang, H. Su, C. Zhang and X. Liao|
|Title||Towards Simulation of Subcellular Calcium Dynamics at Nanometre Resolution|
|Afilliation||Cardiac Modeling, High Performance Computing, Center for Biomedical Computing (SFF), Scientific Computing|
|Project(s)||Center for Biomedical Computing (SFF)|
|Publication Type||Journal Article|
|Year of Publication||2015|
|Journal||International Journal of High Performance Computing Applications|
Numerical simulation of subcellular dynamics with a resolution down to one nanometre can be an important tool for discovering the physiological cause of many heart diseases. The requirement of enormous computational power, however, has made such simulations prohibitive so far. By using up to 12,288 Intel Xeon Phi 31S1P coprocessors on the new hybrid cluster Tianhe-2, which is the new number one supercomputer of the world, we have achieved 1.27 Pflop/s in double precision, which brings us much closer to the nanometre resolution. This is the result of efficiently using the hardware on different levels: (1) a single Xeon Phi (2) a single compute node that consists of a host and three coprocessors, and (3) a huge number of interconnected nodes. To overcome the challenge of programming Intel’s new many-integrated core (MIC) architecture, we have adopted techniques such as vectorization, hierarchical data blocking, register data reuse, offloading computations to the coprocessors, and pipelining computations with intra-/inter-node communications.