Abstract

Automated cell imaging systems facilitate fast and reliable analysis of biological events at the cellular level. In these systems, the first step is usually cell segmentation that greatly affects the success of the subsequent system steps. On the other hand, similar to other image segmentation problems, cell segmentation is an ill-posed problem that typically necessitates the use of domain-specific knowledge to obtain successful segmentations even by human subjects. The approaches that can incorporate this knowledge into their segmentation algorithms have potential to greatly improve segmentation results. In this work, we propose a new approach for the effective segmentation of live cells from phase contrast microscopy. This approach introduces a new set of “smart markers” for a marker-controlled watershed algorithm, for which the identification of its markers is critical. The proposed approach relies on using domain-specific knowledge, in the form of visual characteristics of the cells, to define the markers. We evaluate our approach on a total of 1,954 cells. The experimental results demonstrate that this approach, which uses the proposed definition of smart markers, is quite effective in identifying better markers compared to its counterparts. This will, in turn, be effective in improving the segmentation performance of a marker-controlled watershed algorithm.

Highlights

  • Automated imaging systems are becoming popular to analyze cellular events of fixed or live cells

  • Working with live cell images taken from the KATO-3 cell line, our experiments demonstrate that the proposed algorithm, which uses this new smart marker definition, is effective in finding better markers compared to its counterparts, which will in turn improve the segmentation performance of a markercontrolled watershed algorithm

  • Dataset We conduct our experiments on 44 live cell images of the KATO-3 human gastric cancer cell line

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Summary

Introduction

Automated imaging systems are becoming popular to analyze cellular events of fixed or live cells. These cellular imaging systems have potential for decreasing processing time and for reducing human errors in the analysis. There are several algorithms for the segmentation of fixed cell images from a light or a fluorescence microscope, there exist only few for the segmentation of live cells from phase contrast microscopy. For monolayer isolated cell segmentation, the studies first differentiate cell pixels from the background using global thresholding [1], adaptive thresholding [2,3,4,5], and clustering algorithms [6] and consider the connected components of the cell pixels as the segmented cells

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