3-D Active Meshes: Fast Discrete Deformable Models for Cell Tracking in 3-D Time-Lapse Microscopy
By Alexandre Cecilien Dufour, Roman Thibeaux, Elisabeth Labruyere, Nancy Guillen, Jean-Christophe Olivo-Marin. 2011
150 citations recorded by the source corpus.
Subfields: Biophysics, Computer Vision and Pattern Recognition
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Biophysics
- Fuyong Xing
- Lin F. Yang
- Erik H. W. Meijering
- Oleh Dzyubachyk
- Nicolas Chenouard
- Alexandre Cecilien Dufour
- Martin Maška
- Vannary Meas-Yedid
In Computer Vision and Pattern Recognition
- Lin F. Yang
- Fuyong Xing
- Erik H. W. Meijering
- Oleh Dzyubachyk
- Nicolas Chenouard
- Martin Maška
- Alexandre Cecilien Dufour
- Arrate Muñoz-Barrutia
Citations in the corpus
- A benchmark for comparison of cell tracking algorithms (2014, methodology): “After the ISBI 2013 workshop, the organizing committee confirmed the accuracy of the submitted results and compiled the final rankings presented in this article.”
- Segmentation and Shape Tracking of Whole Fluorescent Cells Based on the Chan–Vese Model (2013, methodology): “Approaches developed for this specific task can broadly be classified [9] as either tracking by detection [10]–[13] or tracking by model evolution [9], [14]–[21].”
- Robust Nucleus/Cell Detection and Segmentation in Digital Pathology and Microscopy Images: A Comprehensive Review (2016, methodology): “improved the framework by using 3-D active meshes to reformulate the problem in the discrete domain such that the computational complexity can be significantly reduced [227].”
- Icy: an open bioimage informatics platform for extended reproducible research (2012, background): “The active contours (two dimensions) 23 and active meshes (three dimensions) 24,25 plug-ins are found in protocols dedicated to segmenting and tracking large, deformable objects (typically cells or nuclei) for studying cell-cell interactions in the immune system 26 , and the morphology and motility…”