TY - JOUR
T1 - A novel cell segmentation method and cell phase identification using Markov model
AU - Zhou, Xiaobo
AU - Li, Fuhai
AU - Yan, Jun
AU - Wong, Stephen T.C.
N1 - Funding Information:
Manuscript received October 14, 2007. First published October 31, 2008; current version published March 3, 2009. This work was supported by the Harvard Center for Neurodegeneration and Repair (HCNR) Center for Bioin-formatics Research Grant, Harvard Medical School. This work was supported by the National Institutes of Health (NIH) under Grant R01 LM008696 and the Bioinformatics Program Grant, Harvard Center for Neurodegeneration and Repair to S. T. C. Wong.
PY - 2009
Y1 - 2009
N2 - Optical microscopy is becoming an important technique in drug discovery and life science research. The approaches used to analyze optical microscopy images are generally classified into two categories: automatic and manual approaches. However, the existing automatic systems are rather limited in dealing with large volume of time-lapse microscopy images because of the complexity of cell behaviors and morphological variance. On the other hand, manual approaches are very time-consuming. In this paper, we propose an effective automated, quantitative analysis system that can be used to segment, track, and quantize cell cycle behaviors of a large population of cells nuclei effectively and efficiently. We use adaptive thresholding and watershed algorithm for cell nuclei segmentation followed by a fragment merging method that combines two scoring models based on trend and no trend features. Using the context information of time-lapse data, the phases of cell nuclei are identified accurately via a Markov model. Experimental results show that the proposed system is effective for nuclei segmentation and phase identification.
AB - Optical microscopy is becoming an important technique in drug discovery and life science research. The approaches used to analyze optical microscopy images are generally classified into two categories: automatic and manual approaches. However, the existing automatic systems are rather limited in dealing with large volume of time-lapse microscopy images because of the complexity of cell behaviors and morphological variance. On the other hand, manual approaches are very time-consuming. In this paper, we propose an effective automated, quantitative analysis system that can be used to segment, track, and quantize cell cycle behaviors of a large population of cells nuclei effectively and efficiently. We use adaptive thresholding and watershed algorithm for cell nuclei segmentation followed by a fragment merging method that combines two scoring models based on trend and no trend features. Using the context information of time-lapse data, the phases of cell nuclei are identified accurately via a Markov model. Experimental results show that the proposed system is effective for nuclei segmentation and phase identification.
KW - Cell phase identification
KW - Continuous Markov model
KW - Nuclei segmentation
KW - Time-lapse fluorescence microscopy
KW - Tracking
UR - http://www.scopus.com/inward/record.url?scp=63349108493&partnerID=8YFLogxK
U2 - 10.1109/TITB.2008.2007098
DO - 10.1109/TITB.2008.2007098
M3 - Article
C2 - 19272857
AN - SCOPUS:63349108493
SN - 1089-7771
VL - 13
SP - 152
EP - 157
JO - IEEE Transactions on Information Technology in Biomedicine
JF - IEEE Transactions on Information Technology in Biomedicine
IS - 2
ER -