A flexible and robust approach for segmenting cell nuclei from 2D microscopy images using supervised learning and template matching

被引:57
作者
Chen, Cheng [1 ]
Wang, Wei [1 ,2 ]
Ozolek, John A. [3 ]
Rohde, Gustavo K. [1 ,4 ,5 ]
机构
[1] Carnegie Mellon Univ, Dept Biomed Engn, Ctr Bioimage Informat, Pittsburgh, PA 15213 USA
[2] Beijing Jiaotong Univ, Sch Elect & Informat Engn, Dept Elect & Informat Engn, Beijing, Peoples R China
[3] Childrens Hosp Pittsburgh, Dept Pathol, Pittsburgh, PA 15201 USA
[4] Carnegie Mellon Univ, Dept Elect & Comp Engn, Pittsburgh, PA 15213 USA
[5] Carnegie Mellon Univ, Computat Biol Program, Pittsburgh, PA 15213 USA
关键词
segmentation; nuclei; template matching; nonrigid registration; cross correlation; TIME-LAPSE MICROSCOPY; AUTOMATIC SEGMENTATION; TISSUE-SECTIONS; UNSUPERVISED SEGMENTATION; CLUSTERED NUCLEI; SELECTION METHOD; ACTIVE CONTOURS; CANCER-TISSUE; CLASSIFICATION; TRACKING;
D O I
10.1002/cyto.a.22280
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a new supervised learning-based template matching approach for segmenting cell nuclei from microscopy images. The method uses examples selected by a user for building a statistical model that captures the texture and shape variations of the nuclear structures from a given dataset to be segmented. Segmentation of subsequent, unlabeled, images is then performed by finding the model instance that best matches (in the normalized cross correlation sense) local neighborhood in the input image. We demonstrate the application of our method to segmenting nuclei from a variety of imaging modalities, and quantitatively compare our results to several other methods. Quantitative results using both simulated and real image data show that, while certain methods may work well for certain imaging modalities, our software is able to obtain high accuracy across several imaging modalities studied. Results also demonstrate that, relative to several existing methods, the template-based method we propose presents increased robustness in the sense of better handling variations in illumination, variations in texture from different imaging modalities, providing more smooth and accurate segmentation borders, as well as handling better cluttered nuclei. (c) 2013 International Society for Advancement of Cytometry
引用
收藏
页码:495 / 507
页数:13
相关论文
共 67 条
[1]   High-throughput analysis of multispectral images of breast cancer tissue [J].
Adiga, Umesh ;
Malladi, Ravikanth ;
Fernandez-Gonzalez, Rodrigo ;
de Solorzano, Carlos Ortiz .
IEEE TRANSACTIONS ON IMAGE PROCESSING, 2006, 15 (08) :2259-2268
[2]   Improved Automatic Detection and Segmentation of Cell Nuclei in Histopathology Images [J].
Al-Kofahi, Yousef ;
Lassoued, Wiem ;
Lee, William ;
Roysam, Badrinath .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2010, 57 (04) :841-852
[3]  
[Anonymous], 2006, Digital Image Processing
[4]  
[Anonymous], 2005, International Journal of Advance Research in Computer Science and Management Studies
[5]   Unsupervised cell nucleus segmentation with active contours [J].
Bamford, P ;
Lovell, B .
SIGNAL PROCESSING, 1998, 71 (02) :203-213
[6]  
Bengtsson E., 2004, Pattern Recognition and Image Analysis, V14, P157
[7]   CellProfiler: image analysis software for identifying and quantifying cell phenotypes [J].
Carpenter, Anne E. ;
Jones, Thouis Ray ;
Lamprecht, Michael R. ;
Clarke, Colin ;
Kang, In Han ;
Friman, Ola ;
Guertin, David A. ;
Chang, Joo Han ;
Lindquist, Robert A. ;
Moffat, Jason ;
Golland, Polina ;
Sabatini, David M. .
GENOME BIOLOGY, 2006, 7 (10)
[8]   Active contours without edges [J].
Chan, TF ;
Vese, LA .
IEEE TRANSACTIONS ON IMAGE PROCESSING, 2001, 10 (02) :266-277
[9]   Constraint factor graph cut-based active contour method for automated cellular image segmentation in RNAi screening [J].
Chen, C. ;
Li, H. ;
Zhou, X. ;
Wong, S. T. C. .
JOURNAL OF MICROSCOPY, 2008, 230 (02) :177-191
[10]   Automated segmentation, classification, and tracking of cancer cell nuclei in time-lapse microscopy [J].
Chen, XW ;
Zhou, XB ;
Wong, STC .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2006, 53 (04) :762-766