A novel cell segmentation method and cell phase identification using Markov model. Academic Article uri icon

Overview

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.

publication date

  • March 1, 2009

Research

keywords

  • Cell Cycle
  • Cell Nucleus
  • Image Processing, Computer-Assisted
  • Markov Chains
  • Microscopy, Fluorescence
  • Pattern Recognition, Automated

Identity

PubMed Central ID

  • PMC2846548

Scopus Document Identifier

  • 63349108493

Digital Object Identifier (DOI)

  • 10.1109/TITB.2008.2007098

PubMed ID

  • 19272857

Additional Document Info

volume

  • 13

issue

  • 2