Abstract

BackgroundMany cell lines currently used in medical research, such as cancer cells or stem cells, grow in confluent sheets or colonies. The biology of individual cells provide valuable information, thus the separation of touching cells in these microscopy images is critical for counting, identification and measurement of individual cells. Over-segmentation of single cells continues to be a major problem for methods based on morphological watershed due to the high level of noise in microscopy cell images. There is a need for a new segmentation method that is robust over a wide variety of biological images and can accurately separate individual cells even in challenging datasets such as confluent sheets or colonies.ResultsWe present a new automated segmentation method called FogBank that accurately separates cells when confluent and touching each other. This technique is successfully applied to phase contrast, bright field, fluorescence microscopy and binary images. The method is based on morphological watershed principles with two new features to improve accuracy and minimize over-segmentation.First, FogBank uses histogram binning to quantize pixel intensities which minimizes the image noise that causes over-segmentation. Second, FogBank uses a geodesic distance mask derived from raw images to detect the shapes of individual cells, in contrast to the more linear cell edges that other watershed-like algorithms produce.We evaluated the segmentation accuracy against manually segmented datasets using two metrics. FogBank achieved segmentation accuracy on the order of 0.75 (1 being a perfect match). We compared our method with other available segmentation techniques in term of achieved performance over the reference data sets. FogBank outperformed all related algorithms. The accuracy has also been visually verified on data sets with 14 cell lines across 3 imaging modalities leading to 876 segmentation evaluation images.ConclusionsFogBank produces single cell segmentation from confluent cell sheets with high accuracy. It can be applied to microscopy images of multiple cell lines and a variety of imaging modalities. The code for the segmentation method is available as open-source and includes a Graphical User Interface for user friendly execution.Electronic supplementary materialThe online version of this article (doi:10.1186/s12859-014-0431-x) contains supplementary material, which is available to authorized users.

Highlights

  • Many cell lines currently used in medical research, such as cancer cells or stem cells, grow in confluent sheets or colonies

  • Many cell lines that are currently being studied for medical purposes, such as cancer cell lines, grow in confluent sheets

  • It is preferred that the developed method can analyze a multitude of image types, for example, phase contrast, differential interference contrast, and fluorescence images, as they are typically obtained in biomedical science

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Summary

Introduction

Many cell lines currently used in medical research, such as cancer cells or stem cells, grow in confluent sheets or colonies. There is a need for a new segmentation method that is robust over a wide variety of biological images and can accurately separate individual cells even in challenging datasets such as confluent sheets or colonies. Many cell lines that are currently being studied for medical purposes, such as cancer cell lines, grow in confluent sheets. These cell sheets typically exhibit cell line specific biological properties such as the morphology of the sheet, protein expression, proliferation rate, and invasive/metastatic potential. One of the requirements of an automated image analysis method is high accuracy single cell segmentation for individual time steps and its applicability to a wide range of cell types. It is preferred that the developed method can analyze a multitude of image types, for example, phase contrast, differential interference contrast, and fluorescence images, as they are typically obtained in biomedical science

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