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 languageEnglish
Pages (from-to)152-157
Number of pages6
JournalIEEE Transactions on Information Technology in Biomedicine
Volume13
Issue number2
DOIs
StatePublished - 2009

Keywords

  • Cell phase identification
  • Continuous Markov model
  • Nuclei segmentation
  • Time-lapse fluorescence microscopy
  • Tracking

Fingerprint

Dive into the research topics of 'A novel cell segmentation method and cell phase identification using Markov model'. Together they form a unique fingerprint.

Cite this