Literature DB >> 8496727

Maximum a posteriori estimation with Good's roughness for three-dimensional optical-sectioning microscopy.

S Joshi1, M I Miller.   

Abstract

The three-dimensional image-reconstruction problem solved here for optical-sectioning microscopy is to estimate the fluorescence intensity lambda(x), where x epsilon R3, given a series of Poisson counting process measurements [Mj(dx)]jJ = 1, each with intensity [formula: see text] with [formula: see text] being the point spread of the optics focused to the jth plane and sj(y) the detection probability for detector point y at focal depth j. A maximum a posteriori reconstruction generated by inducing a prior distribution on the space of images via Good's three-dimensional rotationally invariant roughness penalty [formula: see text] It is proven that the sequence of iterates that is generated by using the expectation maximization algorithm is monotonically increasing in posterior probability, with stable points of the iteration satisfying the necessary maximizer conditions of the maximum a posteriori solution. The algorithms were implemented on the DECmpp-SX, a 64 x 64 parallel processor, running at < 2 s/(64(3), 3-D iteration). Results are demonstrated from simulated as well as amoebae and volvox data. We study performance comparisons of the algorithms for the missing-data problems corresponding to fast data collection for rapid motion studies in which every other focal plane is removed and for imaging with limited detector areas and efficiency.

Mesh:

Year:  1993        PMID: 8496727     DOI: 10.1364/josaa.10.001078

Source DB:  PubMed          Journal:  J Opt Soc Am A        ISSN: 0740-3232            Impact factor:   2.129


  6 in total

1.  Covisualization by computational optical-sectioning microscopy of integrin and associated proteins at the cell membrane of living onion protoplasts.

Authors:  J S Gens; C Reuzeau; K W Doolittle; J G McNally; B G Pickard
Journal:  Protoplasma       Date:  1996       Impact factor: 3.356

2.  Measure and model a 3-D space-variant PSF for fluorescence microscopy image deblurring.

Authors:  Yemeng Chen; Mengmeng Chen; Li Zhu; Jane Y Wu; Sidan Du; Yang Li
Journal:  Opt Express       Date:  2018-05-28       Impact factor: 3.894

3.  An open-source deconvolution software package for 3-D quantitative fluorescence microscopy imaging.

Authors:  Y Sun; P Davis; E A Kosmacek; F Ianzini; M A Mackey
Journal:  J Microsc       Date:  2009-12       Impact factor: 1.758

4.  Blind Depth-variant Deconvolution of 3D Data in Wide-field Fluorescence Microscopy.

Authors:  Boyoung Kim; Takeshi Naemura
Journal:  Sci Rep       Date:  2015-05-07       Impact factor: 4.379

5.  The 95F unconventional myosin is required for proper organization of the Drosophila syncytial blastoderm.

Authors:  V Mermall; K G Miller
Journal:  J Cell Biol       Date:  1995-06       Impact factor: 10.539

6.  Bayesian-based deconvolution fluorescence microscopy using dynamically updated nonstationary expectation estimates.

Authors:  Alexander Wong; Xiao Yu Wang; Maud Gorbet
Journal:  Sci Rep       Date:  2015-06-08       Impact factor: 4.379

  6 in total

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