(Updated on 2013/2/13)
ID:O-1
Principal developer
Shu TAKAGI, Team Leader, RIKEN
General description
ZZ-EFSI aims the fluid-structure interaction analyses to analyze and predict behaviors of a soft human body for medical application
Computational model
- Finite difference modeling. The solid structure and fluid are identified with a density function (or VOF).
- The solid structure and fluid are all incompressible and described with the different stress terms
Computational method
SMAC method、4-Color SOR
Parallelization
Domain decomposition method
Required language and library
FORTRAN90, C++, MPI, OpenMP, SPHERE
Status of code for public release
Source code is available through ISLIM download site
Maximum computing size in present experiences
- Number of voxels:960x960x960 (884,736,000 elements)
- Parallel computing with 8,192 cores
- Required memory/disk storage: 400GB/8TB
Expected computing size in K computer
- Number of voxels: 40000x4000x4000 (640 billion elements)
- Whole body high resolution blood stream analysis, which data is generated from the MRI images in the demonstration experiments
- Required memory/disk storage: 300TB/6PB.
Figure 1. Whole body blood stream simulation including the material properties, such as in blood vessels.
What does the code enable?
- Blood stream computation covering large blood vessels to capillary vessels including red blood cells and blood platelets
- The simulation is driven directly by the medical data like CT scanner data and MRI data. This enables personalized simulation promptly after the doctor's diagnosis.
ID:O-2
Principal developer
Kenichi ISHIKAWA, Associate Professor, University of Tokyo
General description
The code analyses the spatial dose distribution in a whole body from the medical-purpose heavy particle beam by Monte Carlo method for voxel data. The newly developed domain decomposition Monte Carlo technique allows very large voxel data treatment
Computational model
The domain decomposition
Computational method
Monte Carlo method
Parallelization
The history parallelization by the domain decomposition
Required language and library
FORTRAN77, Fortran90, MPI
Status of code for public release
Source code is available through ISLIM download site.
Maximum computing size in present experiences
- The dose distribution in a whole human body voxel phantom
- The number of voxels: 502×234×860 voxels (whole body) using 1,024 cores of the QUEST/RICC
Expected computing size in K computer
- A whole human body voxel phantom divided by 0.3 mm cubic
- The number of voxels: 1640×890×5630 voxels
- The number of cores: 640 thousands of cores.
Figure 1. The dose distributions of a human body voxel phantom for the assumed the 149 MeV/u carbon beam injected to lung. The three figures show the contribution from all particles (left), from ions (center), and from neutrons (right).
What does the code enable?
- The precise and exact spatial dose distribution for even much non-uniform portion
- The beam wise contribution by ion species, neutron, and photon, which are useful to evaluate biological effects and the secondary cancer's risk analysis.
ID:O-3
Principal developer
Kohei OKITA, Nihon University
General description
The ultrasound propagation simulation for the cancer treatment using High-Intensity Focused Ultrasound (HIFU)
Computational model
Basic equations of the ultrasound propagation for multicomponent media are solved using the n-th order spatial and the second-order time difference schemes (Okita et al., Int. J. Numer. Meth. Fluids 2011; 65:43–66).
Computational method
Finite Difference Time Domain (FDTD) method
Parallelization
The hybrid parallelization by the domain decomposition
Required language and library
Fortran90, C++, MPI, OpenMP, SPHERE
Status of code for public release
Source code is available through ISLIM download site
Maximum computing size in present experiences
- The number of meshes: 1400×1200×1200(2,016,000,000 nodes)
- The number of cores: 256 to 8192 cores
- Required memory/disk storage: 484 GB/1.5 TB
Expected computing size in K computer
- The number of meshes: 1.28 to 4.32 trillion nodes
- Required memory/disk storage: 31-103 TB/90-300 TB (640 thousands of cores)
Figure 1. HIFU for a brain cancer through a skull using an array transducer
What does the code enable?
- Prediction of the treatment region using the simulation with the human body model derived from medical images
- Simulation assisted focus-control HIFU for the deep cancer on which ultrasounds can’t correctly focus
- Support of the development of HIFU device and the safety evaluation of the device in clinical trials for the approval.
- Pre-operative planning for the minimally-invasive HIFU therapy using the simulation of an individual body.
ID:O-4
Principal developer
Toshiaki HISADA, Professor, University of Tokyo
General description
The heart muscle cell models including internal structure (microscopic model) are distributed to each finite element of the heart model (macroscopic model). Both the models are coupled and solved simultaneously using the homogenization method.
Computational model
The finite element methods
Computational method
The sparse matrix solvers by both iterative and direct methods
Parallelization
The hybrid parallelization / the flat MPI parallelization
Required language and library
FORTRAN 90, MPI, Open MP
Status of code for public release
Not released for public.
Maximum computing size in present experiences
- About 26,000 DOFs/cell x 8000 cells
- The biventricular macroscopic model with more than 8,000 elements
- A 8,000-core parallelization on a x86 cluster
- Required memory/disk storage: 4GB x 1000/10-100 GB
Expected computing size in K computer
- About 200,000 DOFs/cell x 640,000 cells
- A whole heart model with more than 640,000 elements
- Parallelization for 640,000 cores
- Required memory/disk storage: 16GB x 80,000/3GB x 80,000.
Figure 1. UT-Heart simulates the heart beats and blood ejection from microscopic events.
What does the code enable?
- Multiscale simulation of a finely meshed whole heart model for practical use will be enabled with almost ideal scalability
- Validation based on clinical data is ongoing from various angles at the University of Tokyo Hospital towards clinical applicatio
- The macroscopic heart simulator was already used for the design of Implantable Cardioverter Defibrillator and brought a breakthrough
- Relationship between the microscopic abnormality regarding functional proteins or ion channels in a cell and the macroscopic heart disease such as hypertrophic cardiomyopathy or long QT syndrome will be understood.