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1.
Nat Methods ; 17(7): 749, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-32591761

RESUMO

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

2.
Nat Methods ; 17(7): 734-740, 2020 07.
Artigo em Inglês | MEDLINE | ID: mdl-32541853

RESUMO

An outstanding challenge in single-molecule localization microscopy is the accurate and precise localization of individual point emitters in three dimensions in densely labeled samples. One established approach for three-dimensional single-molecule localization is point-spread-function (PSF) engineering, in which the PSF is engineered to vary distinctively with emitter depth using additional optical elements. However, images of dense emitters, which are desirable for improving temporal resolution, pose a challenge for algorithmic localization of engineered PSFs, due to lateral overlap of the emitter PSFs. Here we train a neural network to localize multiple emitters with densely overlapping Tetrapod PSFs over a large axial range. We then use the network to design the optimal PSF for the multi-emitter case. We demonstrate our approach experimentally with super-resolution reconstructions of mitochondria and volumetric imaging of fluorescently labeled telomeres in cells. Our approach, DeepSTORM3D, enables the study of biological processes in whole cells at timescales that are rarely explored in localization microscopy.


Assuntos
Aprendizado Profundo , Imageamento Tridimensional/métodos , Imagem Individual de Molécula/métodos , Fenômenos Biológicos , Redes Neurais de Computação , Telômero/ultraestrutura
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