TABLE 2.
Main soma quantification methods for mesoscale connectivity.
| Soma quantification method | Sample preparation/microscopy | Principle |
| Kim et al. (2015) | DAPI stained nuclei | Intensity threshold |
| Frasconi et al. (2014) | GFP transgenic mice | Adaptation of intensity threshold: mean shift clustering to detect soma centers, supervised semantic deconvolution by means of neural networks for image enhancement and manifold learning for filtering false positives |
| ClearMap | YFP | Nuclei detection with background subtraction, filters, morphological operations, and 3D peak detection, followed by watershed segmentation and volume-based filtering to identify cells. |
| MIRACL Pipeline | YFP + DTI registering | Segmentation workflow in ImageJ, utilizing optimized pre-processing, morphological analysis algorithms, and a parallelized feature extraction algorithm for 3D cellular features. |
| CellPose (Stringer et al., 2021; Oltmer et al., 2023) | Light microscopy, HE stained histopathological images | A simulated diffusion process generates spatial gradients pointing toward the center of a cell, and a neural network trained on these gradients, along with pixel categorization, forms a gradient vector field used to predict masks by constructing a dynamical system with fixed points. |
| Suite2p (Pachitariu et al., 2017) | Two-photon calcium images | Greedy segmentation of nearby pixels |
| Hu et al. (2021) | Nissl stained | Modified 3D fully connected Unet |
| Wei et al. (2023) | fMOST | Lightweight neural network for quick soma detection in low resolution, followed by a network with multi-scale context and a module for precise soma localization. |
DAPI, 4′,6-diamidino-2-phenylindole; GFP, green fluorescent protein; YFP, yellow fluorescent protein; DTI, diffusion tensor imaging; fMOST, fluorescence micro-optical sectioning tomography; 3D, three-dimensional; HE, Hematoxylin and eosin stain.