A Semi-Markov Model for Mitosis Segmentation in Time-Lapse Phase Contrast Microscopy Image Sequences of Stem Cell Populations

被引:61
作者
Liu, An-An [1 ]
Li, Kang [2 ]
Kanade, Takeo [3 ]
机构
[1] Tianjin Univ, Sch Elect Informat Engn, Tianjin 300072, Peoples R China
[2] Microsoft Corp, Redmond, WA 98052 USA
[3] Carnegie Mellon Univ, Inst Robot, Pittsburgh, PA 15213 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Hidden conditional random fields; large-scale cell population; mitosis detection; phase contrast microscopy; sequence segmentation; semi-Markov model; LINEAGE CONSTRUCTION; TRACKING;
D O I
10.1109/TMI.2011.2169495
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
We propose a semi-Markov model trained in a max-margin learning framework for mitosis event segmentation in large-scale time-lapse phase contrast microscopy image sequences of stem cell populations. Our method consists of three steps. First, we apply a constrained optimization based microscopy image segmentation method that exploits phase contrast optics to extract candidate subsequences in the input image sequence that contains mitosis events. Then, we apply a max-margin hidden conditional random field (MM-HCRF) classifier learned from human-annotated mitotic and nonmitotic sequences to classify each candidate subsequence as a mitosis or not. Finally, a max-margin semi-Markov model (MM-SMM) trained on manually-segmented mitotic sequences is utilized to reinforce the mitosis classification results, and to further segment each mitosis into four predefined temporal stages. The proposed method outperforms the event-detection CRF model recently reported by Huh et al. as well as several other competing methods in very challenging image sequences of multipolar-shaped C3H10T1/2 mesenchymal stem cells. For mitosis detection, an overall precision of 95.8% and a recall of 88.1% were achieved. For mitosis segmentation, the mean and standard deviation for the localization errors of the start and end points of all mitosis stages were well below 1 and 2 frames, respectively. In particular, an overall temporal location error of 0.73 +/- 1.29 frames was achieved for locating daughter cell birth events.
引用
收藏
页码:359 / 369
页数:11
相关论文
共 46 条
[21]   Computer vision tracking of stemness [J].
Li, Kang ;
Miller, Eric D. ;
Chen, Mei ;
Kanade, Takeo ;
Weiss, Lee E. ;
Campbell, Phil G. .
2008 IEEE INTERNATIONAL SYMPOSIUM ON BIOMEDICAL IMAGING: FROM NANO TO MACRO, VOLS 1-4, 2008, :847-+
[22]   Mitosis cell identification with conditional random fields [J].
Liang, Lichen ;
Zhou, Xiaobo ;
Li, Fuhai ;
Wong, Stephen T. C. ;
Huckins, Jeremy ;
King, Randy W. .
2007 IEEE/NIH LIFE SCIENCE SYSTEMS AND APPLICATIONS WORKSHOP, 2007, :9-+
[23]  
Liu A-A, 2010, Proceedings 2010 7th IEEE International Symposium on Biomedical Imaging: From Nano to Macro, P580, DOI 10.1109/ISBI.2010.5490279
[24]   Distinctive image features from scale-invariant keypoints [J].
Lowe, DG .
INTERNATIONAL JOURNAL OF COMPUTER VISION, 2004, 60 (02) :91-110
[25]  
McCallum A., 2003, Proc Ninet Conf Uncertain Artif Intell, P403
[26]  
McCallum A., 2000, ICML
[27]   SEMI-SMOOTH AND SEMI-CONVEX FUNCTIONS IN CONSTRAINED OPTIMIZATION [J].
MIFFLIN, R .
SIAM JOURNAL ON CONTROL AND OPTIMIZATION, 1977, 15 (06) :959-972
[28]  
Morency L.P., 2007, Proc. Computer Vision and Pattern Recognition, P1, DOI DOI 10.1109/CVPR.2007.383299
[29]   THRESHOLD SELECTION METHOD FROM GRAY-LEVEL HISTOGRAMS [J].
OTSU, N .
IEEE TRANSACTIONS ON SYSTEMS MAN AND CYBERNETICS, 1979, 9 (01) :62-66
[30]  
Padfield DR, 2006, I S BIOMED IMAGING, P1036