Computational simulation of cellular proliferation using a meshless method
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.22/22028 |
Resumo: | Background and objective: During cell proliferation, cells grow and divide in order to obtain two new genetically identical cells. Understanding this process is crucial to comprehend other biological processes. Computational models and algorithms have emerged to study this process and several examples can be found in the literature. The objective of this work was to develop a new computational model capable of simulating cell proliferation. This model was developed using the Radial Point Interpolation Method, a meshless method that, to the knowledge of the authors, was never used to solve this type of problem. Since the efficiency of the model strongly depends on the efficiency of the meshless method itself, the optimal numbers of integration points per integration cell and of nodes for each influence-domain were investigated. Irregular nodal meshes were also used to study their influence on the algorithm. Methods: For the first time, an iterative discrete model solved by the Radial Point Interpolation Method based on the Galerkin weak form was used to establish the system of equations from the reactiondiffusion integro-differential equations, following a new phenomenological law proposed by the authors that describes the growth of a cell over time while dependant on oxygen and glucose availability. The discretization flexibility of the meshless method allows to explicitly follow the geometric changes of the cell until the division phase. Results: It was found that an integration scheme of 6 × 6 per integration cell and influence-domains with only seven nodes allows to predict the cellular growth and division with the best balance between the relative error and the computing cost. Also, it was observed that using irregular meshes do not influence the solution. Conclusions: Even in a preliminary phase, the obtained results are promising, indicating that the algorithm might be a potential tool to study cell proliferation since it can predict cellular growth and division. Moreover, the Radial Point Interpolation Method seems to be a suitable method to study this type of process, even when irregular meshes are used. However, to optimize the algorithm |
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Computational simulation of cellular proliferation using a meshless methodIntegration pointsInfluence domainsMeshless methodsCell proliferationNumerical simulationBackground and objective: During cell proliferation, cells grow and divide in order to obtain two new genetically identical cells. Understanding this process is crucial to comprehend other biological processes. Computational models and algorithms have emerged to study this process and several examples can be found in the literature. The objective of this work was to develop a new computational model capable of simulating cell proliferation. This model was developed using the Radial Point Interpolation Method, a meshless method that, to the knowledge of the authors, was never used to solve this type of problem. Since the efficiency of the model strongly depends on the efficiency of the meshless method itself, the optimal numbers of integration points per integration cell and of nodes for each influence-domain were investigated. Irregular nodal meshes were also used to study their influence on the algorithm. Methods: For the first time, an iterative discrete model solved by the Radial Point Interpolation Method based on the Galerkin weak form was used to establish the system of equations from the reactiondiffusion integro-differential equations, following a new phenomenological law proposed by the authors that describes the growth of a cell over time while dependant on oxygen and glucose availability. The discretization flexibility of the meshless method allows to explicitly follow the geometric changes of the cell until the division phase. Results: It was found that an integration scheme of 6 × 6 per integration cell and influence-domains with only seven nodes allows to predict the cellular growth and division with the best balance between the relative error and the computing cost. Also, it was observed that using irregular meshes do not influence the solution. Conclusions: Even in a preliminary phase, the obtained results are promising, indicating that the algorithm might be a potential tool to study cell proliferation since it can predict cellular growth and division. Moreover, the Radial Point Interpolation Method seems to be a suitable method to study this type of process, even when irregular meshes are used. However, to optimize the algorithmThis work was supported by Ministério da Ciência, Tecnologia e Ensino Superior - Fundação para a Ciência e a Tecnologia (Portugal) [grant number SFRH/BD/146272/2019]; and LAETA [project number UIDB/50022/2020].ElsevierRepositório Científico do Instituto Politécnico do PortoBarbosa, M.I.A.Belinha, JorgeJorge, R.M. NatalCarvalho, A.X.20222035-01-01T00:00:00Z2022-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/22028eng10.1016/j.cmpb.2022.106974metadata only accessinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T13:18:23Zoai:recipp.ipp.pt:10400.22/22028Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:42:06.445502Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Computational simulation of cellular proliferation using a meshless method |
title |
Computational simulation of cellular proliferation using a meshless method |
spellingShingle |
Computational simulation of cellular proliferation using a meshless method Barbosa, M.I.A. Integration points Influence domains Meshless methods Cell proliferation Numerical simulation |
title_short |
Computational simulation of cellular proliferation using a meshless method |
title_full |
Computational simulation of cellular proliferation using a meshless method |
title_fullStr |
Computational simulation of cellular proliferation using a meshless method |
title_full_unstemmed |
Computational simulation of cellular proliferation using a meshless method |
title_sort |
Computational simulation of cellular proliferation using a meshless method |
author |
Barbosa, M.I.A. |
author_facet |
Barbosa, M.I.A. Belinha, Jorge Jorge, R.M. Natal Carvalho, A.X. |
author_role |
author |
author2 |
Belinha, Jorge Jorge, R.M. Natal Carvalho, A.X. |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Repositório Científico do Instituto Politécnico do Porto |
dc.contributor.author.fl_str_mv |
Barbosa, M.I.A. Belinha, Jorge Jorge, R.M. Natal Carvalho, A.X. |
dc.subject.por.fl_str_mv |
Integration points Influence domains Meshless methods Cell proliferation Numerical simulation |
topic |
Integration points Influence domains Meshless methods Cell proliferation Numerical simulation |
description |
Background and objective: During cell proliferation, cells grow and divide in order to obtain two new genetically identical cells. Understanding this process is crucial to comprehend other biological processes. Computational models and algorithms have emerged to study this process and several examples can be found in the literature. The objective of this work was to develop a new computational model capable of simulating cell proliferation. This model was developed using the Radial Point Interpolation Method, a meshless method that, to the knowledge of the authors, was never used to solve this type of problem. Since the efficiency of the model strongly depends on the efficiency of the meshless method itself, the optimal numbers of integration points per integration cell and of nodes for each influence-domain were investigated. Irregular nodal meshes were also used to study their influence on the algorithm. Methods: For the first time, an iterative discrete model solved by the Radial Point Interpolation Method based on the Galerkin weak form was used to establish the system of equations from the reactiondiffusion integro-differential equations, following a new phenomenological law proposed by the authors that describes the growth of a cell over time while dependant on oxygen and glucose availability. The discretization flexibility of the meshless method allows to explicitly follow the geometric changes of the cell until the division phase. Results: It was found that an integration scheme of 6 × 6 per integration cell and influence-domains with only seven nodes allows to predict the cellular growth and division with the best balance between the relative error and the computing cost. Also, it was observed that using irregular meshes do not influence the solution. Conclusions: Even in a preliminary phase, the obtained results are promising, indicating that the algorithm might be a potential tool to study cell proliferation since it can predict cellular growth and division. Moreover, the Radial Point Interpolation Method seems to be a suitable method to study this type of process, even when irregular meshes are used. However, to optimize the algorithm |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022 2022-01-01T00:00:00Z 2035-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.22/22028 |
url |
http://hdl.handle.net/10400.22/22028 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1016/j.cmpb.2022.106974 |
dc.rights.driver.fl_str_mv |
metadata only access info:eu-repo/semantics/openAccess |
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metadata only access |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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