Zobrazeno 1 - 9
of 9
pro vyhledávání: '"ocis:(100.6640) Superresolution"'
Autor:
Kevin O'Holleran, Michael Shaw
Publikováno v:
Biomedical Optics Express
The use of structured illumination in fluorescence microscopy allows the suppression of out of focus light and an increase in effective spatial resolution. In this paper we consider different approaches for reconstructing 2D structured illumination i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0c7b433b765381ec3cf14365613645c
http://europepmc.org/articles/PMC4132990
http://europepmc.org/articles/PMC4132990
Autor:
Alex Small
Publikováno v:
Biomedical Optics Express
We consider acquisition schemes that maximize the fraction of images that contain only a single activated molecule (as opposed to multiple activated molecules) in superresolution localization microscopy of fluorescent probes. During a superresolution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59dd6f649552752d1a894aa37d2cfadf
http://europepmc.org/articles/PMC3207365
http://europepmc.org/articles/PMC3207365
Publikováno v:
Biomedical Optics Express
Many biological structures of interest are beyond the diffraction limit of conventional microscopes and their visualization requires application of super-resolution techniques. Such techniques have found remarkable success in surpassing the diffracti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6aa91a6c4b9f509943c219c5112744a
https://pubmed.ncbi.nlm.nih.gov/22876348
https://pubmed.ncbi.nlm.nih.gov/22876348
Publikováno v:
Optics Express
Bio-mechanism investigations demand single particle tracking with high spatial and temporal resolutions which require single fluorophore 3D localization measurements with matching precision and speed. Although the precision for lateral-localization m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75fbe8a6cbdfeced2f84b9f4a4c0da6d
https://pubmed.ncbi.nlm.nih.gov/22330542
https://pubmed.ncbi.nlm.nih.gov/22330542
Publikováno v:
Biomedical Optics Express
We present an imaging method, dSLIM, that combines a novel deconvolution algorithm with spatial light interference microscopy (SLIM), to achieve 2.3x resolution enhancement with respect to the diffraction limit. By exploiting the sparsity of the phas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0a0fe4eed12382b71a1bf6e1315b4e9
https://pubmed.ncbi.nlm.nih.gov/21750760
https://pubmed.ncbi.nlm.nih.gov/21750760
Publikováno v:
Optics Express
Structured illumination (SI) has long been regarded as a nonquantitative technique for obtaining sectioned microscopic images. Its lack of quantitative results has restricted the use of SI sectioning to qualitative imaging experiments, and has also l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8dfcd4746c13725a5c8ec804487f88a
https://doi.org/10.1364/oe.20.000403
https://doi.org/10.1364/oe.20.000403
Publikováno v:
Biomedical Optics Express
Single molecule localization based super-resolution imaging techniques require repeated localization of many single emitters. We describe a method that uses the maximum likelihood estimator to localize multiple emitters simultaneously within a single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8cf198485d85caf15f9d69a5fbe8492
https://doi.org/10.1364/boe.2.001377
https://doi.org/10.1364/boe.2.001377
Publikováno v:
Biomedical Optics Express
3D STORM is one of the leading methods for super-resolution imaging, with resolution down to 10 nm in the lateral direction, and 30–50 nm in the axial direction. However, there is one important requirement to perform this type of imaging: making dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6ee38bb1579e9b1663d51d366a8870c
https://infoscience.epfl.ch/record/187186
https://infoscience.epfl.ch/record/187186
Publikováno v:
Scopus-Elsevier
Biomedical Optics Express 2 (2011), Nr. 2
Biomedical Optics Express
Biomedical Optics Express 2 (2011), Nr. 2
Biomedical Optics Express
Multiphoton fluorescence microscopy based on femtosecond laser scanning is a powerful technique for three dimensional optical sectioning in life sciences. The method is based on the simultaneous absorption of two or three photons in the focal volume
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db61d2c832796e8645cf21cf942b7194
http://www.scopus.com/inward/record.url?eid=2-s2.0-84893586436&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84893586436&partnerID=MN8TOARS