Literature DB >> 26033916

Performance and sensitivity evaluation of 3D spot detection methods in confocal microscopy.

Karel Štěpka1, Pavel Matula1, Petr Matula1, Stefan Wörz2, Karl Rohr2, Michal Kozubek1.   

Abstract

Reliable 3D detection of diffraction-limited spots in fluorescence microscopy images is an important task in subcellular observation. Generally, fluorescence microscopy images are heavily degraded by noise and non-specifically stained background, making reliable detection a challenging task. In this work, we have studied the performance and parameter sensitivity of eight recent methods for 3D spot detection. The study is based on both 3D synthetic image data and 3D real confocal microscopy images. The synthetic images were generated using a simulator modeling the complete imaging setup, including the optical path as well as the image acquisition process. We studied the detection performance and parameter sensitivity under different noise levels and under the influence of uneven background signal. To evaluate the parameter sensitivity, we propose a novel measure based on the gradient magnitude of the F1 score. We measured the success rate of the individual methods for different types of the image data and found that the type of image degradation is an important factor. Using the F1 score and the newly proposed sensitivity measure, we found that the parameter sensitivity is not necessarily proportional to the success rate of a method. This also provided an explanation why the best performing method for synthetic data was outperformed by other methods when applied to the real microscopy images. On the basis of the results obtained, we conclude with the recommendation of the HDome method for data with relatively low variations in quality, or the Sorokin method for image sets in which the quality varies more. We also provide alternative recommendations for high-quality images, and for situations in which detailed parameter tuning might be deemed expensive.
© 2015 International Society for Advancement of Cytometry.

Keywords:  3D imaging; diffraction-limited spot detection; fluorescence microscopy; parameter sensitivity

Mesh:

Year:  2015        PMID: 26033916     DOI: 10.1002/cyto.a.22692

Source DB:  PubMed          Journal:  Cytometry A        ISSN: 1552-4922            Impact factor:   4.355


  5 in total

1.  upU-Net Approaches for Background Emission Removal in Fluorescence Microscopy.

Authors:  Alessandro Benfenati
Journal:  J Imaging       Date:  2022-05-20

2.  DNA double-strand breaks in human induced pluripotent stem cell reprogramming and long-term in vitro culturing.

Authors:  Pavel Simara; Lenka Tesarova; Daniela Rehakova; Pavel Matula; Stanislav Stejskal; Ales Hampl; Irena Koutna
Journal:  Stem Cell Res Ther       Date:  2017-03-21       Impact factor: 6.832

Review 3.  Image-Based Profiling of Synaptic Connectivity in Primary Neuronal Cell Culture.

Authors:  Peter Verstraelen; Michiel Van Dyck; Marlies Verschuuren; Nachiket D Kashikar; Rony Nuydens; Jean-Pierre Timmermans; Winnok H De Vos
Journal:  Front Neurosci       Date:  2018-06-26       Impact factor: 4.677

4.  In vivo large-scale analysis of Drosophila neuronal calcium traces by automated tracking of single somata.

Authors:  Felipe Delestro; Lisa Scheunemann; Mélanie Pedrazzani; Paul Tchenio; Thomas Preat; Auguste Genovesio
Journal:  Sci Rep       Date:  2020-04-28       Impact factor: 4.379

5.  Reprogramming of Adult Peripheral Blood Cells into Human Induced Pluripotent Stem Cells as a Safe and Accessible Source of Endothelial Cells.

Authors:  Pavel Simara; Lenka Tesarova; Daniela Rehakova; Simon Farkas; Barbara Salingova; Katerina Kutalkova; Eva Vavreckova; Pavel Matula; Petr Matula; Lenka Veverkova; Irena Koutna
Journal:  Stem Cells Dev       Date:  2017-12-11       Impact factor: 3.272

  5 in total

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