Feature Decomposition Based Saliency Detection in Electron Cryo-Tomograms
This addresses the difficulty of segmenting complex subcellular structures in ECT for researchers in structural biology, though it is incremental as it complements existing methods rather than replacing them.
The paper tackles the problem of automatic segmentation of cellular components in Electron Cryo-Tomography (ECT) images by proposing a saliency detection method that identifies subregions standing out from the background, which successfully labels most salient regions detected by humans and filters out non-cellular areas to speed up subsequent processing.
Electron Cryo-Tomography (ECT) allows 3D visualization of subcellular structures at the submolecular resolution in close to the native state. However, due to the high degree of structural complexity and imaging limits, the automatic segmentation of cellular components from ECT images is very difficult. To complement and speed up existing segmentation methods, it is desirable to develop a generic cell component segmentation method that is 1) not specific to particular types of cellular components, 2) able to segment unknown cellular components, 3) fully unsupervised and does not rely on the availability of training data. As an important step towards this goal, in this paper, we propose a saliency detection method that computes the likelihood that a subregion in a tomogram stands out from the background. Our method consists of four steps: supervoxel over-segmentation, feature extraction, feature matrix decomposition, and computation of saliency. The method produces a distribution map that represents the regions' saliency in tomograms. Our experiments show that our method can successfully label most salient regions detected by a human observer, and able to filter out regions not containing cellular components. Therefore, our method can remove the majority of the background region, and significantly speed up the subsequent processing of segmentation and recognition of cellular components captured by ECT.