Superpixel-based segmentation of muscle fibers in multi-channel microscopy. Issue 5 (December 2016)

• Record Type: Journal Article
• Authors: Nguyen, Binh; Heemskerk, Hans; So, Peter; Tucker-Kellogg, Lisa
• Is Part Of: BMC systems biology. Volume 10:Issue 5(2016)
• Page Start: 39
• Page End: 50
• Publication Date: 2016-12
• Subjects: Superpixel -- Segmentation -- Muscle fibers -- Confetti fluorescence -- Multi-channel microscopy; Biological systems -- Periodicals; Biology -- Research -- Periodicals; Cell physiology -- Periodicals; Genes -- Analysis -- Periodicals; 571
• DOI: 10.1186/s12918-016-0372-2
• Languages: English
• ISSNs: 1752-0509

Abstract

Abstract Background Confetti fluorescence and other multi-color genetic labelling strategies are useful for observing stem cell regeneration and for other problems of cell lineage tracing. One difficulty of such strategies is segmenting the cell boundaries, which is a very different problem from segmenting color images from the real world. This paper addresses the difficulties and presents a superpixel-based framework for segmentation of regenerated muscle fibers in mice. Results We propose to integrate an edge detector into a superpixel algorithm and customize the method for multi-channel images. The enhanced superpixel method outperforms the original and another advanced superpixel algorithm in terms of both boundary recall and under-segmentation error. Our framework was applied to cross-section and lateral section images of regenerated muscle fibers from confetti-fluorescent mice. Compared with "ground-truth" segmentations, our framework yielded median Dice similarity coefficients of 0.92 and higher. Conclusion Our segmentation framework is flexible and provides very good segmentations of multi-color muscle fibers. We anticipate our methods will be useful for segmenting a variety of tissues in confetti fluorecent mice and in mice with similar multi-color labels.