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dc.contributor.authorMandracchia, Biagio 
dc.contributor.authorLiu, Wenhao
dc.contributor.authorHua, Xuanwen
dc.contributor.authorForghani, Parvin
dc.contributor.authorLee, Soojung
dc.contributor.authorHou, Jessica
dc.contributor.authorNie, Shuyi
dc.contributor.authorXu, Chunhui
dc.contributor.authorJia, Shu
dc.date.accessioned2023-09-26T11:35:04Z
dc.date.available2023-09-26T11:35:04Z
dc.date.issued2023-09
dc.identifier.citationSci Adv. 2023 Sep;9(35):eadg9245.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16508
dc.descriptionIncluye: artículo, material suplementario, videos y software.es_ES
dc.description.abstractFluorescence microscopy is one of the most indispensable and informative driving forces for biological research, but the extent of observable biological phenomena is essentially determined by the content and quality of the acquired images. To address the different noise sources that can degrade these images, we introduce an algorithm for multiscale image restoration through optimally sparse representation (MIRO). MIRO is a deterministic framework that models the acquisition process and uses pixelwise noise correction to improve image quality. Our study demonstrates that this approach yields a remarkable restoration of the fluorescence signal for a wide range of microscopy systems, regardless of the detector used (e.g., electron-multiplying charge-coupled device, scientific complementary metal-oxide semiconductor, or photomultiplier tube). MIRO improves current imaging capabilities, enabling fast, low-light optical microscopy, accurate image analysis, and robust machine intelligence when integrated with deep neural networks. This expands the range of biological knowledge that can be obtained from fluorescence microscopy.es_ES
dc.description.sponsorshipWe acknowledge the support of the National Institutes of Health grants R35GM124846 (to S.J.) and R01AA028527 (to C.X.), the National Science Foundation grants BIO2145235 and EFMA1830941 (to S.J.), and Marvin H. and Nita S. Floyd Research Fund (to S.J.). This research project was supported, in part, by the Emory University Integrated Cellular Imaging Microscopy Core and by PHS Grant UL1TR000454 from the Clinical and Translational Science Award Program, National Institutes of Health, and National Center for Advancing Translational Sciences.es_ES
dc.language.isoenges_ES
dc.publisherAmerican Association for the Advancement of Science (AAAS) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subject.meshAlgorithms es_ES
dc.subject.meshElectrons es_ES
dc.subject.meshMicroscopy, Fluorescence es_ES
dc.subject.meshImage Processing, Computer-Assistedes_ES
dc.subject.meshNeural Networks, Computeres_ES
dc.titleOptimal sparsity allows reliable system-aware restoration of fluorescence microscopy imageses_ES
dc.typeresearch articlees_ES
dc.rights.licenseAtribución-NoComercial 4.0 Internacional*
dc.identifier.pubmedID37647399es_ES
dc.format.volume9es_ES
dc.format.number35es_ES
dc.format.pageeadg9245es_ES
dc.identifier.doi10.1126/sciadv.adg9245es_ES
dc.contributor.funderNational Institutes of Health (Estados Unidos) es_ES
dc.contributor.funderNational Science Foundation (Estados Unidos) es_ES
dc.contributor.funderOffice of Emerging Frontiers and Multidisciplinary Activities (Estados Unidos)es_ES
dc.contributor.funderEmory University (Estados Unidos)es_ES
dc.contributor.funderNational Center for Advancing Translational Sciences (Estados Unidos) es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn2375-2548es_ES
dc.relation.publisherversionhttps://doi.org/10.1126/sciadv.adg9245es_ES
dc.identifier.journalScience advanceses_ES
dc.repisalud.centroISCIII::Centro Nacional de Microbiología::Unidades Comunes Científico-Técnicas (UCCT)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES


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Este Item está sujeto a una licencia Creative Commons: Atribución-NoComercial 4.0 Internacional