4.7 Article

TrackMate: An open and extensible platform for single-particle tracking

Journal

METHODS
Volume 115, Issue -, Pages 80-90

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2016.09.016

Keywords

Single-particle tracking; Phototoxicity; Clathin-mediated endocytosis; Image analysis; Open-source software; Microscopy

Funding

  1. European commission FP7 ICT
  2. Laboratory for Optical and Computational Instrumentation at the UW-Madison
  3. National Science Foundation [1121998]
  4. Stanford University
  5. Fiji, ImageJ and KNIME communities
  6. Direct For Biological Sciences
  7. Div Of Molecular and Cellular Bioscience [1121998] Funding Source: National Science Foundation

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We present TrackMate, an open source Fiji plugin for the automated, semi-automated, and manual tracking of single-particles. It offers a versatile and modular solution that works out of the box for end users, through a simple and intuitive user interface. It is also easily scriptable and adaptable, operating equally well on 1D over time, 2D over time, 3D over time, or other single and multi-channel image variants. TrackMate provides several visualization and analysis tools that aid in assessing the relevance of results. The utility of TrackMate is further enhanced through its ability to be readily customized to meet specific tracking problems. TrackMate is an extensible platform where developers can easily write their own detection, particle linking, visualization or analysis algorithms within the TrackMate environment. This evolving framework provides researchers with the opportunity to quickly develop and optimize new algorithms based on existing TrackMate modules without the need of having to write de novo user interfaces, including visualization, analysis and exporting tools. The current capabilities of TrackMate are presented in the context of three different biological problems. First, we perform Caenorhabditis-elegans lineage analysis to assess how light-induced damage during imaging impairs its early development. Our TrackMate-based lineage analysis indicates the lack of a cell-specific light-sensitive mechanism. Second, we investigate the recruitment of NEMO (NE-KB essential modulator) clusters in fibroblasts after stimulation by the cytokine IL-1 and show that photodamage can generate artifacts in the shape of TrackMate characterized movements that confuse motility analysis. Finally, we validate the use of TrackMate for quantitative lifetime analysis of clathrin-mediated endocytosis in plant cells. (C) 2016 The Author(s). Published by Elsevier Inc.

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