WormID-Benchmark: Extracting Whole-Brain Neural Dynamics of C. elegans At the Neuron Resolution
में बचाया:
| में प्रकाशित: | bioRxiv (Jan 7, 2025) |
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| मुख्य लेखक: | |
| अन्य लेखक: | , , , , , , , , , , |
| प्रकाशित: |
Cold Spring Harbor Laboratory Press
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| विषय: | |
| ऑनलाइन पहुंच: | Citation/Abstract Full Text - PDF Full text outside of ProQuest |
| टैग: |
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| 001 | 3152304836 | ||
| 003 | UK-CbPIL | ||
| 022 | |a 2692-8205 | ||
| 024 | 7 | |a 10.1101/2025.01.06.631621 |2 doi | |
| 035 | |a 3152304836 | ||
| 045 | 0 | |b d20250107 | |
| 100 | 1 | |a Adhinarta, Jason | |
| 245 | 1 | |a WormID-Benchmark: Extracting Whole-Brain Neural Dynamics of C. elegans At the Neuron Resolution | |
| 260 | |b Cold Spring Harbor Laboratory Press |c Jan 7, 2025 | ||
| 513 | |a Working Paper | ||
| 520 | 3 | |a The nematode C. elegans is a well-studied model organism for characterizing the structure, connectivity, and function of a complete nervous system. Recent technical breakthroughs in 3D light microscopy and fluorescent protein tagging of individual neurons have brought us closer to capturing the neural dynamics of the worm at whole-brain resolution. Nevertheless, capturing a complete map of neural dynamics using these high-resolution recordings requires solving three specific challenges: i) detection of individual neurons in fluorescence videos, ii) identification of these neurons according to their anatomically defined classes, and iii) tracking of neural positions over time. Successfully addressing these challenges with high sensitivity, specificity, and throughput can enable us to analyze a large population sample, providing unprecedented insights into the structure and function of an entire brain at single-neuron resolution, a feat previously unaccomplished in any organism. To facilitate this scientific goal, we have curated publicly available annotated datasets from 118 worms across five distinct laboratories and established systematic benchmarks, decomposing the overarching objective into three well-defined tasks: i) neural detection, ii) identification, and iii) spatiotemporal tracking. Our preliminary analysis has revealed considerable room for improvement in existing state-of-the-art computational methods. Consequently, we envision that our WormID-Benchmark can catalyze efforts by a broad audience specializing in computer vision to develop robust and accurate methods that significantly enhance the throughput of generating annotated whole-brain neural dynamics datasets. We make our benchmark results reproducible; our code is publicly available at https://github.com/focolab/WormND.Competing Interest StatementThe authors have declared no competing interest.Footnotes* We remove the figures at the end.* https://github.com/focolab/WormND | |
| 653 | |a Neurons | ||
| 653 | |a Light microscopy | ||
| 653 | |a Structure-function relationships | ||
| 653 | |a Nervous system | ||
| 653 | |a Functional anatomy | ||
| 653 | |a Neural networks | ||
| 653 | |a Marking and tracking techniques | ||
| 653 | |a Brain mapping | ||
| 700 | 1 | |a Dong, Jizheng | |
| 700 | 1 | |a He, Tianxiao | |
| 700 | 1 | |a Sprague, Daniel | |
| 700 | 1 | |a Wan, Jia | |
| 700 | 1 | |a Hyun Jee Lee | |
| 700 | 1 | |a Yu, Zikai | |
| 700 | 1 | |a Lu, Hang | |
| 700 | 1 | |a Yemini, Eviatar | |
| 700 | 1 | |a Kato, Saul | |
| 700 | 1 | |a Varol, Erdem | |
| 700 | 1 | |a Donglai Wei | |
| 773 | 0 | |t bioRxiv |g (Jan 7, 2025) | |
| 786 | 0 | |d ProQuest |t Biological Science Database | |
| 856 | 4 | 1 | |3 Citation/Abstract |u https://www.proquest.com/docview/3152304836/abstract/embedded/75I98GEZK8WCJMPQ?source=fedsrch |
| 856 | 4 | 0 | |3 Full Text - PDF |u https://www.proquest.com/docview/3152304836/fulltextPDF/embedded/75I98GEZK8WCJMPQ?source=fedsrch |
| 856 | 4 | 0 | |3 Full text outside of ProQuest |u https://www.biorxiv.org/content/10.1101/2025.01.06.631621v2 |