Abstract

BackgroundSegmenting cell nuclei in microscopic images has become one of the most important routines in modern biological applications. With the vast amount of data, automatic localization, i.e. detection and segmentation, of cell nuclei is highly desirable compared to time-consuming manual processes. However, automated segmentation is challenging due to large intensity inhomogeneities in the cell nuclei and the background.ResultsWe present a new method for automated progressive localization of cell nuclei using data-adaptive models that can better handle the inhomogeneity problem. We perform localization in a three-stage approach: first identify all interest regions with contrast-enhanced salient region detection, then process the clusters to identify true cell nuclei with probability estimation via feature-distance profiles of reference regions, and finally refine the contours of detected regions with regional contrast-based graphical model. The proposed region-based progressive localization (RPL) method is evaluated on three different datasets, with the first two containing grayscale images, and the third one comprising of color images with cytoplasm in addition to cell nuclei. We demonstrate performance improvement over the state-of-the-art. For example, compared to the second best approach, on the first dataset, our method achieves 2.8 and 3.7 reduction in Hausdorff distance and false negatives; on the second dataset that has larger intensity inhomogeneity, our method achieves 5% increase in Dice coefficient and Rand index; on the third dataset, our method achieves 4% increase in object-level accuracy.ConclusionsTo tackle the intensity inhomogeneities in cell nuclei and background, a region-based progressive localization method is proposed for cell nuclei localization in fluorescence microscopy images. The RPL method is demonstrated highly effective on three different public datasets, with on average 3.5% and 7% improvement of region- and contour-based segmentation performance over the state-of-the-art.

Highlights

  • Segmenting cell nuclei in microscopic images has become one of the most important routines in modern biological applications

  • We suggest that the proposed region-based progressive localization (RPL) method can be potentially extended to other localization problems, if the objects of interest can be modeled as regions with distinct features from the surrounding background

  • On dataset 3, the presence of cytoplasm causes many cell nuclei to clutter into one region during the initial segmentation; this leads to FN

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Summary

Introduction

Segmenting cell nuclei in microscopic images has become one of the most important routines in modern biological applications. With the vast amount of data, automatic localization, i.e. detection and segmentation, of cell nuclei is highly desirable compared to time-consuming manual processes. Automated segmentation is challenging due to large intensity inhomogeneities in the cell nuclei and the background. Microscopic image analysis is becoming an enabling technology for modern systems-biology research, and cell nucleus segmentation is often the first step in the pipeline. The segmentation performance remains unsatisfactory in many cases. On the popular public databases [1], the state-of-the-art segmentation accuracies are just around 85%. The challenges of automated cell nucleus segmentation mainly arise from two imaging artifacts, as shown

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