Axon tracking in serial block-face scanning electron microscopy

被引:73
作者
Jurrus, Elizabeth [1 ]
Hardy, Melissa [2 ]
Tasdizen, Tolga [1 ]
Fletcher, P. Thomas [1 ]
Koshevoy, Pavel [1 ]
Chien, Chi-Bin [2 ]
Denk, Winfried [3 ]
Whitaker, Ross [1 ]
机构
[1] Univ Utah, Sci Comp & Imaging Inst, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT USA
[3] Max Planck Inst Med Res, Heidelberg, Germany
关键词
Image processing; Tracking; Kalman filtering; Active contours; Scanning electron microscopy; Neurobiology; OBJECT DETECTION; SEGMENTATION; IMAGES; CELL;
D O I
10.1016/j.media.2008.05.002
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Electron microscopy is an important modality for the analysis of neuronal structures in neurobiology. We address the problem of tracking axons across large distances in volumes acquired by serial block-face scanning electron microscopy (SBFSEM). Tracking, for this application, is defined as the segmentation of an axon that spans a volume using similar features between slices. This is a challenging problem due to the small cross-sectional size of axons and the low signal-to-noise ratio in our SBFSEM images. A carefully engineered algorithm using Kalman-snakes and optical flow computation is presented. Axon tracking is initialized with user clicks or automatically using the watershed segmentation algorithm, which identifies axon centers. Multiple axons are tracked from slice to slice through a volume, updating the positions and velocities in the model and providing constraints to maintain smoothness between slices. Validation results indicate that this algorithm can significantly speed up the task of manual axon tracking. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:180 / 188
页数:9
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