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dc.contributor.authorSekh, Arif Ahmed
dc.contributor.authorOpstad, Ida Sundvor
dc.contributor.authorGodtliebsen, Gustav
dc.contributor.authorBirgisdottir, Åsa Birna
dc.contributor.authorAhluwalia, Balpreet Singh
dc.contributor.authorAgarwal, Krishna
dc.contributor.authorPrasad, Dilip K.
dc.date.accessioned2022-02-24T09:10:28Z
dc.date.available2022-02-24T09:10:28Z
dc.date.issued2021-12-15
dc.description.abstractSegmenting subcellular structures in living cells from fluorescence microscope images is a ground truth (GT)-deficient problem. The microscopes’ three-dimensional blurring function, finite optical resolution due to light diffraction, finite pixel resolution and the complex morphological manifestations of the structures all contribute to GT-hardness. Unsupervised segmentation approaches are quite inaccurate. Therefore, manual segmentation relying on heuristics and experience remains the preferred approach. However, this process is tedious, given the countless structures present inside a single cell, and generating analytics across a large population of cells or performing advanced artificial intelligence tasks such as tracking are greatly limited. Here we bring modelling and deep learning to a nexus for solving this GT-hard problem, improving both the accuracy and speed of subcellular segmentation. We introduce a simulation-supervision approach empowered by physics-based GT, which presents two advantages. First, the physics-based GT resolves the GT-hardness. Second, computational modelling of all the relevant physical aspects assists the deep learning models in learning to compensate, to a great extent, for the limitations of physics and the instrument. We show extensive results on the segmentation of small vesicles and mitochondria in diverse and independent living- and fixed-cell datasets. We demonstrate the adaptability of the approach across diverse microscopes through transfer learning, and illustrate biologically relevant applications of automated analytics and motion analysis.en_US
dc.identifier.citationSekh AA, Opstad IS, Godtliebsen G, Birgisdottir Åb, Ahluwalia BS, Agarwal K, Prasad DK. Physics-based machine learning for subcellular segmentation in living cells. Nature Machine Intelligence. 2021:1-12en_US
dc.identifier.cristinIDFRIDAID 1974873
dc.identifier.doi10.1038/s42256-021-00420-0
dc.identifier.issn2522-5839
dc.identifier.urihttps://hdl.handle.net/10037/24124
dc.language.isoengen_US
dc.publisherNatureen_US
dc.relation.journalNature Machine Intelligence
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/804233/Norway/Label-free 3D morphological nanoscopy for studying sub-cellular dynamics in live cancer cells with high spatio-temporal resolution/3D-nanoMorph/en_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2021 The Author(s)en_US
dc.titlePhysics-based machine learning for subcellular segmentation in living cellsen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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