Fast and robust optical flow for time-lapse microscopy using super-voxels

被引:37
作者
Amat, Fernando [1 ]
Myers, Eugene W. [2 ]
Keller, Philipp J. [1 ]
机构
[1] Howard Hughes Med Inst, Ashburn, VA 20147 USA
[2] Max Planck Inst Mol Cell Biol & Genet, D-01307 Dresden, Germany
关键词
IMAGE REGISTRATION; COMPUTATION; MOTION;
D O I
10.1093/bioinformatics/bts706
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Optical flow is a key method used for quantitative motion estimation of biological structures in light microscopy. It has also been used as a key module in segmentation and tracking systems and is considered a mature technology in the field of computer vision. However, most of the research focused on 2D natural images, which are small in size and rich in edges and texture information. In contrast, 3D time-lapse recordings of biological specimens comprise up to several terabytes of image data and often exhibit complex object dynamics as well as blurring due to the point-spread-function of the microscope. Thus, new approaches to optical flow are required to improve performance for such data. Results: We solve optical flow in large 3D time-lapse microscopy datasets by defining a Markov random field (MRF) over super-voxels in the foreground and applying motion smoothness constraints between super-voxels instead of voxel-wise. This model is tailored to the specific characteristics of light microscopy datasets: super-voxels help registration in textureless areas, the MRF over super-voxels efficiently propagates motion information between neighboring cells and the background subtraction and super-voxels reduce the dimensionality of the problem by an order of magnitude. We validate our approach on large 3D time-lapse datasets of Drosophila and zebrafish development by analyzing cell motion patterns. We show that our approach is, on average, 10 x faster than commonly used optical flow implementations in the Insight Tool-Kit (ITK) and reduces the average flow end point error by 50% in regions with complex dynamic processes, such as cell divisions.
引用
收藏
页码:373 / 380
页数:8
相关论文
共 40 条
[1]   Computation and visualization of three-dimensional soft tissue motion in the orbit [J].
Abràmoff, MD ;
Viergever, MA .
IEEE TRANSACTIONS ON MEDICAL IMAGING, 2002, 21 (04) :296-304
[2]   SLIC Superpixels Compared to State-of-the-Art Superpixel Methods [J].
Achanta, Radhakrishna ;
Shaji, Appu ;
Smith, Kevin ;
Lucchi, Aurelien ;
Fua, Pascal ;
Suesstrunk, Sabine .
IEEE TRANSACTIONS ON PATTERN ANALYSIS AND MACHINE INTELLIGENCE, 2012, 34 (11) :2274-2281
[3]  
[Anonymous], 2011 17 INT C DIG SI
[4]  
[Anonymous], 2009, BMVC
[5]  
Ayvaci Alper., 2010, Advances_in_neural_information_processing systems, P100
[6]   A Database and Evaluation Methodology for Optical Flow [J].
Baker, Simon ;
Scharstein, Daniel ;
Lewis, J. P. ;
Roth, Stefan ;
Black, Michael J. ;
Szeliski, Richard .
INTERNATIONAL JOURNAL OF COMPUTER VISION, 2011, 92 (01) :1-31
[7]   The robust estimation of multiple motions: Parametric and piecewise-smooth flow fields [J].
Black, MJ ;
Anandan, P .
COMPUTER VISION AND IMAGE UNDERSTANDING, 1996, 63 (01) :75-104
[8]   Large Displacement Optical Flow: Descriptor Matching in Variational Motion Estimation [J].
Brox, Thomas ;
Malik, Jitendra .
IEEE TRANSACTIONS ON PATTERN ANALYSIS AND MACHINE INTELLIGENCE, 2011, 33 (03) :500-513
[9]   Lucas/Kanade meets Horn/Schunck: Combining local and global optic flow methods [J].
Bruhn A. ;
Weickert J. ;
Schnörr C. .
International Journal of Computer Vision, 2005, 61 (3) :1-21
[10]   Mapping the Spatiotemporal Dynamics of Calcium Signaling in Cellular Neural Networks Using Optical Flow [J].
Buibas, Marius ;
Yu, Diana ;
Nizar, Krystal ;
Silva, Gabriel A. .
ANNALS OF BIOMEDICAL ENGINEERING, 2010, 38 (08) :2520-2531