dc.contributor.author | Sekh, Arif Ahmed | |
dc.contributor.author | Opstad, Ida Sundvor | |
dc.contributor.author | Godtliebsen, Gustav | |
dc.contributor.author | Birgisdottir, Åsa Birna | |
dc.contributor.author | Ahluwalia, Balpreet Singh | |
dc.contributor.author | Agarwal, Krishna | |
dc.contributor.author | Prasad, Dilip K. | |
dc.date.accessioned | 2022-02-24T09:10:28Z | |
dc.date.available | 2022-02-24T09:10:28Z | |
dc.date.issued | 2021-12-15 | |
dc.description.abstract | Segmenting 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.citation | Sekh 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. 2021:1-12 | en_US |
dc.identifier.cristinID | FRIDAID 1974873 | |
dc.identifier.doi | 10.1038/s42256-021-00420-0 | |
dc.identifier.issn | 2522-5839 | |
dc.identifier.uri | https://hdl.handle.net/10037/24124 | |
dc.language.iso | eng | en_US |
dc.publisher | Nature | en_US |
dc.relation.journal | Nature Machine Intelligence | |
dc.relation.projectID | info: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.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2021 The Author(s) | en_US |
dc.title | Physics-based machine learning for subcellular segmentation in living cells | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |