DocumentCode :
3621818
Title :
Topology preserving STACS segmentation of protein subcellular location images
Author :
L. Coulot;H. Kirschner;A. Chebira;J.M.F. Moura;J. Kovacevic;E.G. Osuna;R.F. Murphy
Author_Institution :
Dept. of Electr. & Comput. Eng., Carnegie Mellon Univ., Pittsburgh, PA, USA
fYear :
2006
fDate :
6/28/1905 12:00:00 AM
Firstpage :
566
Lastpage :
569
Abstract :
We present an algorithm for the segmentation of multicell fluorescence microscopy images. Such images abound and a segmentation algorithm robust to different experimental conditions as well as cell types is becoming a necessity. In cellular imaging, among the most often used segmentation algorithms is seeded watershed. One of its features is that it tends to oversegment, splitting the cells, as well as create segmented regions much larger than a true cell. This can be an advantage (the entire cell is within the region) as well as a disadvantage (a large amount of background noise is included). We present an algorithm which segments with tight contours by building upon an active contour algorithm - STACS, by Pluempitiwiriyawej et al. We adapt the algorithm to suit the needs of our data and use another technique, topology preservation by Han et al., to build our topology preserving STACS (TPSTACS). Our algorithm significantly outperforms the seeded watershed both visually as well as by standard measures of segmentation quality: recall/precision, area similarity and area overlap
Keywords :
"Topology","Image segmentation","Proteins","Fluorescence","Microscopy","Robustness","Background noise","Active contours","Measurement standards","Area measurement"
Publisher :
ieee
Conference_Titel :
Biomedical Imaging: Nano to Macro, 2006. 3rd IEEE International Symposium on
Print_ISBN :
0-7803-9576-X
Type :
conf
DOI :
10.1109/ISBI.2006.1624979
Filename :
1624979
Link To Document :
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