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dc.contributor.authorMartín González, Elena 
dc.contributor.authorMoya Sáez, Elisa
dc.contributor.authorMenchón Lara, Rosa María
dc.contributor.authorRoyuela del Val, Javier
dc.contributor.authorPalencia de Lara, César 
dc.contributor.authorRodríguez Cayetano, Manuel 
dc.contributor.authorSimmross Wattenberg, Federico Jesús 
dc.contributor.authorAlberola López, Carlos 
dc.date.accessioned2021-08-27T11:05:47Z
dc.date.available2021-08-27T11:05:47Z
dc.date.issued2021
dc.identifier.citationComputer Methods and Programs in Biomedicine, 2021, vol. 207, 106143es
dc.identifier.issn0169-2607es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/48168
dc.descriptionProducción Científicaes
dc.description.abstractBackground and objective: Recent research has reported methods that reconstruct cardiac MR images acquired with acceleration factors as high as 15 in Cartesian coordinates. However, the computational cost of these techniques is quite high, taking about 40 min of CPU time in a typical current machine. This delay between acquisition and final result can completely rule out the use of MRI in clinical environments in favor of other techniques, such as CT. In spite of this, reconstruction methods reported elsewhere can be parallelized to a high degree, a fact that makes them suitable for GPU-type computing devices. This paper contributes a vendor-independent, device-agnostic implementation of such a method to reconstruct 2D motion-compensated, compressed-sensing MRI sequences in clinically viable times. Methods: By leveraging our OpenCLIPER framework, the proposed system works in any computing device (CPU, GPU, DSP, FPGA, etc.), as long as an OpenCL implementation is available, and development is significantly simplified versus a pure OpenCL implementation. In OpenCLIPER, the problem is partitioned in independent black boxes which may be connected as needed, while device initialization and maintenance is handled automatically. Parallel implementations of both a groupwise FFD-based registration method, as well as a multicoil extension of the NESTA algorithm have been carried out as processes of OpenCLIPER. Our platform also includes significant development and debugging aids. HIP code and precompiled libraries can be integrated seamlessly as well since OpenCLIPER makes data objects shareable between OpenCL and HIP. This also opens an opportunity to include CUDA source code (via HIP) in prospective developments. Results: The proposed solution can reconstruct a whole 12–14 slice CINE volume acquired in 19–32 coils and 20 phases, with an acceleration factor of ranging 4–8, in a few seconds, with results comparable to another popular platform (BART). If motion compensation is included, reconstruction time is in the order of one minute. Conclusions: We have obtained clinically-viable times in GPUs from different vendors, with delays in some platforms that do not have correspondence with its price in the market. We also contribute a parallel groupwise registration subsystem for motion estimation/compensation and a parallel multicoil NESTA subsystem for -norm problem solving.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.classificationMagnetic resonance imaginges
dc.subject.classificationImagen por resonancia magnéticaes
dc.subject.classificationGraphics processing unites
dc.subject.classificationUnidad de procesamiento gráficoes
dc.subject.classificationOpenCLIPERes
dc.titleA clinically viable vendor-independent and device-agnostic solution for accelerated cardiac MRI reconstructiones
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2021 The Authorses
dc.identifier.doi10.1016/j.cmpb.2021.106143es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0169260721002182?via%3Dihubes
dc.peerreviewedSIes
dc.description.projectMinisterio de Economía, Industria y Competitividad (grant TEC2017-82408-R)es
dc.description.projectAsociación Española Contra el Cáncer (grant PRDVL19001MOYA)es
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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