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Marker-Less stage drift correction in super-resolution microscopy using the single-cluster PHD filter

Marker-Less stage drift correction in super-resolution microscopy using the single-cluster PHD filter
Marker-Less stage drift correction in super-resolution microscopy using the single-cluster PHD filter

Fluorescence microscopy is a technique which allows the imaging of cellular and intracellular dynamics through the activation of fluorescent molecules attached to them. It is a very important technique because it can be used to analyze the behavior of intracellular processes in vivo in contrast to methods like electron microscopy. There are several challenges related to the extraction of meaningful information from images acquired from optical microscopes due to the low contrast between objects and background and the fact that point-like objects are observed as blurred spots due to the diffraction limit of the optical system. Another consideration is that for the study of intracellular dynamics, multiple particles must be tracked at the same time, which is a challenging task due to problems such as the presence of false positives and missed detections in the acquired data. Additionally, the objective of the microscope is not completely static with respect to the cover slip due to mechanical vibrations or thermal expansions which introduces bias in the measurements. In this paper, a Bayesian approach is used to simultaneously track the locations of objects with different motion behaviors and the stage drift using image data obtained from fluorescence microscopy experiments. Namely, detections are extracted from the acquired frames using image processing techniques, and then these detections are used to accurately estimate the particle positions and simultaneously correct the drift introduced by the motion of the sample stage. A single cluster Probability Hypothesis Density (PHD) filter with object classification is used for the estimation of the multiple target state assuming different motion behaviors. The detection and tracking methods are tested and their performance is evaluated on both simulated and real data.

Biomedical imaging, estimation, filtering, microscopy, molecular imaging, particle tracking, probability density function, simultaneous localization and mapping
1932-4553
193-202
Schlangen, Isabel
3c69b082-aadc-49cb-8bf9-8df20a8d2c7a
Franco, José
6f88f0bd-effb-46a2-9a6f-a2062915786d
Houssineau, Jérémie
89988b62-a668-4560-b49f-c1686ba7b584
Pitkeathly, William T.E.
46c8085d-e776-4ec4-95fd-2d537d7d01df
Clark, Daniel
537f80e8-cbe6-41eb-b1d4-31af1f0e6393
Smal, Ihor
fc9ce9b5-de50-4e19-9f5b-f4599ad25f2b
Rickman, Colin
47551504-e58b-40d4-8b99-422196aa4b0b
Schlangen, Isabel
3c69b082-aadc-49cb-8bf9-8df20a8d2c7a
Franco, José
6f88f0bd-effb-46a2-9a6f-a2062915786d
Houssineau, Jérémie
89988b62-a668-4560-b49f-c1686ba7b584
Pitkeathly, William T.E.
46c8085d-e776-4ec4-95fd-2d537d7d01df
Clark, Daniel
537f80e8-cbe6-41eb-b1d4-31af1f0e6393
Smal, Ihor
fc9ce9b5-de50-4e19-9f5b-f4599ad25f2b
Rickman, Colin
47551504-e58b-40d4-8b99-422196aa4b0b

Schlangen, Isabel, Franco, José, Houssineau, Jérémie, Pitkeathly, William T.E., Clark, Daniel, Smal, Ihor and Rickman, Colin (2016) Marker-Less stage drift correction in super-resolution microscopy using the single-cluster PHD filter. IEEE Journal on Selected Topics in Signal Processing, 10 (1), 193-202, [7348657]. (doi:10.1109/JSTSP.2015.2506402).

Record type: Article

Abstract

Fluorescence microscopy is a technique which allows the imaging of cellular and intracellular dynamics through the activation of fluorescent molecules attached to them. It is a very important technique because it can be used to analyze the behavior of intracellular processes in vivo in contrast to methods like electron microscopy. There are several challenges related to the extraction of meaningful information from images acquired from optical microscopes due to the low contrast between objects and background and the fact that point-like objects are observed as blurred spots due to the diffraction limit of the optical system. Another consideration is that for the study of intracellular dynamics, multiple particles must be tracked at the same time, which is a challenging task due to problems such as the presence of false positives and missed detections in the acquired data. Additionally, the objective of the microscope is not completely static with respect to the cover slip due to mechanical vibrations or thermal expansions which introduces bias in the measurements. In this paper, a Bayesian approach is used to simultaneously track the locations of objects with different motion behaviors and the stage drift using image data obtained from fluorescence microscopy experiments. Namely, detections are extracted from the acquired frames using image processing techniques, and then these detections are used to accurately estimate the particle positions and simultaneously correct the drift introduced by the motion of the sample stage. A single cluster Probability Hypothesis Density (PHD) filter with object classification is used for the estimation of the multiple target state assuming different motion behaviors. The detection and tracking methods are tested and their performance is evaluated on both simulated and real data.

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More information

Published date: February 2016
Keywords: Biomedical imaging, estimation, filtering, microscopy, molecular imaging, particle tracking, probability density function, simultaneous localization and mapping

Identifiers

Local EPrints ID: 480204
URI: http://eprints.soton.ac.uk/id/eprint/480204
ISSN: 1932-4553
PURE UUID: 74e62073-997e-4b31-97a1-e74b0aa1c2a3

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Date deposited: 01 Aug 2023 17:04
Last modified: 17 Mar 2024 13:11

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Contributors

Author: Isabel Schlangen
Author: José Franco
Author: Jérémie Houssineau
Author: William T.E. Pitkeathly
Author: Daniel Clark
Author: Ihor Smal
Author: Colin Rickman

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