Literature DB >> 26176413

Quantitative comparison of multiframe data association techniques for particle tracking in time-lapse fluorescence microscopy.

Ihor Smal1, Erik Meijering2.   

Abstract

Biological studies of intracellular dynamic processes commonly require motion analysis of large numbers of particles in live-cell time-lapse fluorescence microscopy imaging data. Many particle tracking methods have been developed in the past years as a first step toward fully automating this task and enabling high-throughput data processing. Two crucial aspects of any particle tracking method are the detection of relevant particles in the image frames and their linking or association from frame to frame to reconstruct the trajectories. The performance of detection techniques as well as specific combinations of detection and linking techniques for particle tracking have been extensively evaluated in recent studies. Comprehensive evaluations of linking techniques per se, on the other hand, are lacking in the literature. Here we present the results of a quantitative comparison of data association techniques for solving the linking problem in biological particle tracking applications. Nine multiframe and two more traditional two-frame techniques are evaluated as a function of the level of missing and spurious detections in various scenarios. The results indicate that linking techniques are generally more negatively affected by missing detections than by spurious detections. If misdetections can be avoided, there appears to be no need to use sophisticated multiframe linking techniques. However, in the practically likely case of imperfect detections, the latter are a safer choice. Our study provides users and developers with novel information to select the right linking technique for their applications, given a detection technique of known quality.
Copyright © 2015 Elsevier B.V. All rights reserved.

Keywords:  Correspondence problem; Fluorescence microscopy; Lagrangian relaxation; Multiframe data association; Object tracking

Mesh:

Year:  2015        PMID: 26176413     DOI: 10.1016/j.media.2015.06.006

Source DB:  PubMed          Journal:  Med Image Anal        ISSN: 1361-8415            Impact factor:   8.545


  6 in total

1.  Quantifying transcription factor binding dynamics at the single-molecule level in live cells.

Authors:  Diego M Presman; David A Ball; Ville Paakinaho; Jonathan B Grimm; Luke D Lavis; Tatiana S Karpova; Gordon L Hager
Journal:  Methods       Date:  2017-03-15       Impact factor: 3.608

2.  Piecewise-Stationary Motion Modeling and Iterative Smoothing to Track Heterogeneous Particle Motions in Dense Environments.

Authors:  Philippe Roudot; Khuloud Jaqaman; Charles Kervrann; Gaudenz Danuser
Journal:  IEEE Trans Image Process       Date:  2017-11       Impact factor: 10.856

3.  Automated Cell Tracking Using Motion Prediction-Based Matching and Event Handling.

Authors:  Fatima Boukari; Sokratis Makrogiannis
Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2018-10-12       Impact factor: 3.710

4.  A review for cell and particle tracking on microscopy images using algorithms and deep learning technologies.

Authors:  Hui-Jun Cheng; Ching-Hsien Hsu; Che-Lun Hung; Chun-Yuan Lin
Journal:  Biomed J       Date:  2021-10-07       Impact factor: 7.892

5.  Automated single particle detection and tracking for large microscopy datasets.

Authors:  Rhodri S Wilson; Lei Yang; Alison Dun; Annya M Smyth; Rory R Duncan; Colin Rickman; Weiping Lu
Journal:  R Soc Open Sci       Date:  2016-05-18       Impact factor: 2.963

6.  A global sampler of single particle tracking solutions for single molecule microscopy.

Authors:  Michael Hirsch; Richard Wareham; Ji W Yoon; Daniel J Rolfe; Laura C Zanetti-Domingues; Michael P Hobson; Peter J Parker; Marisa L Martin-Fernandez; Sumeetpal S Singh
Journal:  PLoS One       Date:  2019-10-28       Impact factor: 3.240

  6 in total

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