Particle detection and tracking in fluorescence time-lapse imaging: a contrario approach

This paper proposes a probabilistic approach for the detection and the tracking of particles in fluorescent time-lapse imaging. In the presence of a very noised and poor-quality data, particles and trajectories can be characterized by an a contrario model, that estimates the probability of observing the structures of interest in random data. This approach, first introduced in the modeling of human visual perception and then successfully applied in many image processing tasks, leads to algorithms that neither require a previous learning stage, nor a tedious parameter tuning and are very robust to noise. Comparative evaluations against a well-established baseline show that the proposed approach outperforms the state of the art.Comment: Published in Journal of Machine Vision and Application

Objective comparison of particle tracking methods

Particle tracking is of key importance for quantitative analysis of intracellular dynamic processes from time-lapse microscopy image data. Because manually detecting and following large numbers of individual particles is not feasible, automated computational methods have been developed for these tasks by many groups. Aiming to perform an objective comparison of methods, we gathered the community and organized an open competition in which participating teams applied their own methods independently to a commonly defined data set including diverse scenarios. Performance was assessed using commonly defined measures. Although no single method performed best across all scenarios, the results revealed clear differences between the various approaches, leading to notable practical conclusions for users and developers

OMEGA: a software tool for the management, analysis, and dissemination of intracellular trafficking data that incorporates motion type classification and quality control [preprint]

MOTIVATION: Particle tracking coupled with time-lapse microscopy is critical for understanding the dynamics of intracellular processes of clinical importance. Spurred on by advances in the spatiotemporal resolution of microscopy and automated computational methods, this field is increasingly amenable to multi-dimensional high-throughput data collection schemes (Snijder et al, 2012). Typically, complex particle tracking datasets generated by individual laboratories are produced with incompatible methodologies that preclude comparison to each other. There is therefore an unmet need for data management systems that facilitate data standardization, meta-analysis, and structured data dissemination. The integration of analysis, visualization, and quality control capabilities into such systems would eliminate the need for manual transfer of data to diverse downstream analysis tools. At the same time, it would lay the foundation for shared trajectory data, particle tracking, and motion analysis standards. RESULTS: Here, we present Open Microscopy Environment inteGrated Analysis (OMEGA), a cross-platform data management, analysis, and visualization system, for particle tracking data, with particular emphasis on results from viral and vesicular trafficking experiments. OMEGA provides easy to use graphical interfaces to implement integrated particle tracking and motion analysis workflows while keeping track of error propagation and data provenance. Specifically, OMEGA: 1) imports image data and metadata from data management tools such as Open Microscopy Environment Remote Objects (OMERO; Allan et al., 2012); 2) tracks intracellular particles moving across time series of image planes; 3) facilitates parameter optimization and trajectory results inspection and validation; 4) performs downstream trajectory analysis and motion type classification; 5) estimates the uncertainty associated with motion analysis; and, 6) facilitates storage and dissemination of analysis results, and analysis definition metadata, on the basis of our newly proposed Minimum Information About Particle Tracking Experiments (MIAPTE; Rigano & Strambio-De-Castillia, 2016; 2017) guidelines in combination with the OME-XML data model (Goldberg et al, 2005)

Quantitative analysis of microscopy

Particle tracking is an essential tool for the study of dynamics of biological processes. The dynamics of these processes happens in three-dimensional (3D) space as the biological structures themselves are 3D. The focus of this thesis is on the development of single particle tracking methods for analysis of the dynamics of biological processes through the use of image processing techniques. Firstly, introduced is a novel particle tracking method that works with two-dimensional (2D) image data. This method uses the theory of Haar-like features for particle detection and trajectory linking is achieved using a combination of three Kalman filters within an interacting multiple models framework. The trajectory linking process utilises an extended state space variable which better describe the morphology and intensity profiles of the particles under investigation at their current position. This tracking method is validated using both 2D synthetically generated images as well as 2D experimentally collected images. It is shown that this method outperforms 14 other stateof-the-art methods. Next this method is used to analyse the dynamics of fluorescently labelled particles using a live-cell fluorescence microscopy technique, specifically a variant of the super-resolution (SR) method PALM, spt-PALM. From this application, conclusions about the organisation of the proteins under investigation at the cell membrane are drawn. Introduced next is a second particle tracking method which is highly efficient and capable of working with both 2D and 3D image data. This method uses a novel Haar-inspired feature for particle detection, drawing inspiration from the type of particles to be detected which are typically circular in 2D space and spherical in 3D image space. Trajectory linking in this method utilises a global nearest neighbour methodology incorporating both motion models to describe the motion of the particles under investigation and a further extended state space variable describing many more aspects of the particles to be linked. This method is validated using a variety of both 2D and 3D synthetic image data. The methods performance is compared with 14 other state-of-the-art methods showing it to be one of the best overall performing methods. Finally, analysis tools to study a SR image restoration method developed by our research group, referred to as Translation Microscopy (TRAM) are investigated [1]. TRAM can be implemented on any standardised microscope and deliver an improvement in resolution of up to 7-fold. However, the results from TRAM and other SR imaging methods require specialised tools to validate and analyse them. Tools have been developed to validate that TRAM performs correctly using a specially designed ground truth. Furthermore, through analysis of results on a biological sample corroborate other published results based on the size of biological structures, showing again that TRAM performs as expected.EPSC