We have implemented SFDA and ATA metrics to comprehensively evalu

We have implemented SFDA and ATA metrics to comprehensively evaluate the performance of detection and tracking of cells on real experimental data. These metrics have gained acceptance by the computer vision research community as they facilitate standardization of procedures. Similar metrics have very recently been proposed in the cell tracking research community as well (Maska et al., 2014). As we have further demonstrated, automating the process of performance evaluation allows for comparison between multiple disparate

tools, for testing the performance at different parameter settings and on different types of experimental data and for assessing the contribution of newly added features to existing algorithms. We have created a separate MATLAB-based software package Selleckchem 17-AAG that we call PACT (Performance Analysis of Cell Tracking), to enable investigators to calculate SFDA MK-1775 chemical structure and ATA based on manually established ground truth. As individual datasets from different labs or different types of experiments are likely to be sufficiently unique, PACT can guide users to decide on the best tool to analyze their data. Data integration is critical for extending our understanding of complex systems and processes. TIAM was structured with this overarching principle in mind to take advantage of multi-channel acquisition afforded by the state-of-the-art

fluorescence microscopy platforms. TIAM is equipped to retrieve and associate features from transmitted light, fluorescence and reflection channels to cell tracks and

track-positions. The insights that we obtained were critically dependent on the integrative analysis facilitated by TIAM. The generic feature extraction procedure that we have employed allows for future developments to characterize patterns in fluorescence from individual cells. It is conceivable that relating the patterns in fluorescence-based readout of critical signaling molecules to each other and to motility parameters in a spatiotemporal manner by live-cell imaging will yield rich mechanistic information (Vilela and Danuser, 2011). VM conceptualized the software work-flow and oversaw the project triclocarban development. WN implemented the detection and tracking algorithms and built the user interface. VM implemented the feature extraction algorithms. RM built the user interface for visualization of tracks. VM tested the software. VM conducted the experiments, established the ground truth and analyzed data. VM and WN conducted the performance analysis. VM and WN wrote the manuscript. MLD and CHW provided overall guidance. All authors discussed the results and approved the manuscript. The following are the supplementary data related to this article. Supplementary material.

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