For eachstimulus,ourextractedcomputational mechanisms areconsistent withprior scientific literature, and in one case yields a new mechanistic hypothesis.

Here we go beyond previous theories to analyze how a simple linear retinal encoding model with different convolutional cell types efficiently encodes naturalistic spatiotemporal movies given a fixed firing rate budget.

Identifying evolutionary correspondences between cell types across species is a fundamental challenge in comparative genomics and evolutionary biology. Existing approaches often rely on either reference-based matching, which imposes asymmetry by designating one species as the reference, or projection-based matching, which may increase computational complexity and obscure biological interpretability at the cell-type level. Here, we present OT-MESH, an unsupervised computational framework leveraging entropy-regularized optimal transport (OT) to systematically determine cross-species cell type homologies. Our method uniquely integrates the Minimize Entropy of Sinkhorn (MESH) technique to refine the OT plan, transforming diffuse transport matrices into sparse, interpretable correspondences. Through systematic evaluation on synthetic datasets, we demonstrate that OT-MESH achieves near-optimal matching accuracy with computational efficiency, while maintaining remarkable robustness to noise. Compared to other OT-based methods like RefCM, OT-MESH provides speedup while achieving comparable accuracy. Applied to retinal bipolar cells (BCs) and retinal ganglion cells (RGCs) from mouse and macaque, OT-MESH accurately recovers known evolutionary relationships and uncovers novel correspondences, one of which was independently validated experimentally. Thus, our framework offers a principled, scalable, and interpretable solution for evolutionary cell type mapping, facilitating deeper insights into cellular specialization and conservation across species.

Many neural circuits are composed of numerous distinct cell types that perform different operations on their inputs, and send their outputs to distinct targets. Therefore, a key step in understanding neural systems is to reliably distinguish cell types. An important example is the retina, for which present-day techniques for identifying cell types are accurate, but very labor-intensive. Here, we develop automated classifiers for functional identification of retinal ganglion cells, the output neurons of the retina, based solely on recorded voltage patterns on a large scale array. We use per-cell classifiers based on features extracted from electro-physiological images (spatiotemporal voltage waveforms) and interspike intervals (autocorrelations). These classifiers achieve high performance in distinguishing between the major ganglion cell classes of the primate retina, but fail in achieving the same accuracy in predicting cell polarities (ON vs. OFF). We then show how to use indicators of functional coupling within populations of ganglion cells (cross-correlation) to infer cell polarities with a matrix completion algorithm. This can result in accurate, fully automated methods for cell type classification.

Neural Information Processing Systems http://nips.cc/

Hirschsprung's disease (HD) is a congenital birth defect diagnosed by identifying the lack of ganglion cells within the colon's muscularis propria, specifically within the myenteric plexus regions. There may be advantages for quantitative assessments of histopathology images of the colon, such as counting the ganglion and assessing their spatial distribution; however, this would be time-intensive for pathologists, costly, and subject to inter- and intra-rater variability. Previous research has demonstrated the potential for deep learning approaches to automate histopathology image analysis, including segmentation of the muscularis propria using convolutional neural networks (CNNs). Recently, Vision Transformers (ViTs) have emerged as a powerful deep learning approach due to their self-attention. This study explores the application of ViTs for muscularis propria segmentation in calretinin-stained histopathology images and compares their performance to CNNs and shallow learning methods. The ViT model achieved a DICE score of 89.9% and Plexus Inclusion Rate (PIR) of 100%, surpassing the CNN (DICE score of 89.2%; PIR of 96.0%) and k-means clustering method (DICE score of 80.7%; PIR 77.4%). Results assert that ViTs are a promising tool for advancing HD-related image analysis.

Many neural circuits are composed of numerous distinct cell types that perform different operations on their inputs, and send their outputs to distinct targets. Therefore, a key step in understanding neural systems is to reliably distinguish cell types. An important example is the retina, for which present-day techniques for identifying cell types are accurate, but very labor-intensive. Here, we develop automated classifiers for functional identification of retinal ganglion cells, the output neurons of the retina, based solely on recorded voltage patterns on a large scale array. We use per-cell classifiers based on features extracted from electrophysiological images (spatiotemporal voltage waveforms) and interspike intervals (autocorrelations). These classifiers achieve high performance in distinguishing between the major ganglion cell classes of the primate retina, but fail in achieving the same accuracy in predicting cell polarities (ON vs. OFF). We then show how to use indicators of functional coupling within populations of ganglion cells (cross-correlation) to infer cell polarities with a matrix completion algorithm. This can result in accurate, fully automated methods for cell type classification.