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Numerical modeling of cardiac electrophysiology at the cellular scale

Project description

Digital twins of cardiac tissue representing cell-to-cell connections

Cardiovascular diseases are the leading cause of death globally. Numerical models of heart function are widely used to gain insight, but greater resolution is urgently needed. Representation of individual cardiac cells and their connections will require tremendous computing power. The EU-funded MICROCARD-2 project aims to address this challenge, building on the previous EuroHPC-2019 MICROCARD project and its exascale platform for cardiac electrophysiology simulations supporting cell-by-cell simulations. MICROCARD-2 plans to reduce communication bandwidth, extend its energy-efficient system code for central and graphics processing units to emerging architectures and enable production of realistic tissue meshes for simulations, among others.

Objective

Cardiac function is coordinated by an electric system whose disorders are among the most frequent causes of death and disease. Numerical models of this complex system are mature 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 makes the problem more complex, harder to solve, and four orders of magnitude larger, necessitating exascale computers.

The EuroHPC-2019 MICROCARD project is developing a simulation platform that can meet this challenge, by a joint effort of HPC experts, numerical scientists, biomedical engineers, and biomedical scientists, from academia and industry. Our proposal is to establish a Centre of Excellence that will consolidate and scale up the MICROCARD results enabling digital twins of cardiac tissue.

With a consortium gathering the core partners of MICROCARD, we will further develop MICROCARD's numerical schemes, moving to second-order spatial discretization. Based on MICROCARD results, we will develop mixed-precision preconditioners and data compression to reduce communication bandwidth. The highly successful efforts towards automated compilation of high-level model descriptions into optimized, energy-efficient system code for different CPUs and GPUs will be extended to upcoming architectures. We will continue efforts to robustify parallel remeshing software and add necessary functionality for parallel mesh partitioning and production of realistic synthetic tissue meshes needed for simulations.

The platform will be benchmarked with realistic test cases and be made accessible for a wide range of users with tailored workflows.

The platform will be adaptable to similar biological systems such as nerves, and several of our products such as improved solvers, preconditioners, remeshers, and partitioners will be reusable in a wide range of applications.

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Programme(s)

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Topic(s)

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Funding Scheme

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HORIZON-JU-RIA - HORIZON JU Research and Innovation Actions

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Call for proposal

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(opens in new window) HORIZON-EUROHPC-JU-2023-COE-03

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Coordinator

UNIVERSITE DE BORDEAUX
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 259 806,25
Address
PLACE PEY BERLAND 35
33000 BORDEAUX
France

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Region
Nouvelle-Aquitaine Aquitaine Gironde
Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 519 612,50

Participants (9)

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