Ca2+ transient detection and segmentation with the Astronomically motivated algorithm for Background Estimation And Transient Segmentation (Astro-BEATS)
Organizations: Dunlap Institute for Astronomy and Astrophysics, University of Toronto, Toronto, Canada · David A. Dunlap Department for Astronomy and Astrophysics, University of Toronto, Toronto, Canada · CERVO Brain Research Center, Québec, Canada · Institute Intelligence and Data, Université Laval, Québec, Canada ·
Abstract
Fluorescence-based Ca-imaging is a powerful tool for studying localized neuronal activity, including miniature Synaptic Calcium Transients, providing real-time insights into synaptic activity. These transients induce only subtle changes in the fluorescence signal, often barely above baseline, which poses a significant challenge for automated synaptic transient detection and segmentation. Detecting astronomical transients similarly requires efficient algorithms that will remain robust over a large field of view with varying noise properties. We leverage techniques used in astronomical transient detection for miniature Synaptic Calcium Transient detection in fluorescence microscopy. We present Astro-BEATS, an automatic miniature Synaptic Calcium Transient segmentation algorithm that incorporates image estimation and source-finding techniques used in astronomy and designed for Ca-imaging videos. Astro-BEATS outperforms current threshold-based approaches for synaptic Ca transient detection and segmentation. The produced segmentation masks can be used to train a supervised deep learning algorithm for improved synaptic Ca transient detection in Ca-imaging data. The speed of Astro-BEATS and its applicability to previously unseen datasets without re-optimization makes it particularly useful for generating training datasets for deep learning-based approaches.
Figures & tables
| Parameter | Astro-BEATS | IDT | AQuA |
|---|---|---|---|
| Computation time | s/frame | s/transient | min/video |
| ( min/video) | ( hr/video) | ||
| Annotation Precision | 0.92 0.06 | 0.94 0.10 | 0.56 0.34 |
| Annotation Recall | 0.75 0.14 | 0.38 0.18 | 0.34 0.22 |
| Annotation F 1 score | 0.81 0.11 | 0.50 0.17 | 0.39 0.26 |
| Segmentation DiCE score | 0.66 0.18 | 0.58 0.21 | 0.41 0.24 |
Appendix figures & tables8 assets
Supplementary material from the paper’s appendix.
Appendix
| Parameter | Description | Range Tested | Value used here |
|---|---|---|---|
| Initial brightness threshold | |||
| Minimum points per cluster | 500 | ||
| Maximum spatial separation | pixels | 7 pixels | |
| Maximum time separation | frames | 2 Frames |
| Parameter | Description |
|---|---|
| Area of 2D projection of detection within aperture | |
| in number of square pixels | |
| (1px 2 = 0.0256 m 2 ). | |
| Note that detections with footprint area larger | |
| than our aperture ( Section 2.2.3 ) will be | |
| recorded as filling our entire aperture, having |
| Parameter | Range Tested | Optimal Value Found |
|---|---|---|
| Smoothing | 0.5 | |
| Minimum size of groups of | ||
| connected tentative active voxels | voxels | 10 voxels |
Microscopy Image Analysis
Microscopy image analysis uses computational methods to detect, segment, track, reconstruct, and quantify structures in scientific images.
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