Abstract
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.
Original language | English (US) |
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Pages (from-to) | 152-157 |
Number of pages | 6 |
Journal | IEEE Transactions on Information Technology in Biomedicine |
Volume | 13 |
Issue number | 2 |
DOIs | |
State | Published - 2009 |
Keywords
- Cell phase identification
- Continuous Markov model
- Nuclei segmentation
- Time-lapse fluorescence microscopy
- Tracking
ASJC Scopus subject areas
- Electrical and Electronic Engineering
- Biotechnology
- Computer Science Applications
- Medicine(all)