TY - GEN
T1 - One-shot Active Neuron Localization with in vivo Fluorescence Image Sequences
AU - Cheng, Wensheng
AU - Li, Zhenghong
AU - Ren, Jiaxiang
AU - Rout, Reeti
AU - Pan, Yingtian
AU - Du, Congwu
AU - Ling, Haibin
N1 - Publisher Copyright:
© 2025 IEEE.
PY - 2025
Y1 - 2025
N2 - Active neuron localization with in vivo fluorescence image sequences for neuron activity analysis traditionally relies on manual observation. To reduce labor costs, we cast this process as a novel one-shot active neuron localization task requiring minimal user intervention, i.e., only one active neuron template. Observing that neurons switch between active and inactive states over time, we formulate this task as a new one-shot multiple instance learning (MIL) problem, and propose an MIL-based framework integrating multifaceted properties. First, patch proposals are generated heuristically and combined into sequence proposals with temporal profile-based filtering. Second, a deep neural network is trained with self-supervision as the feature extractor. Third, the template feature and the patch feature of sequence proposals are extracted and compared to classify sequences and identify neuron positions in an MIL fashion. Experiments with in vivo data demonstrate our method's clear performance advantage over comparison methods, providing a foundation for future physiological analysis. The code is available at https://github.com/Spritea/OANL.
AB - Active neuron localization with in vivo fluorescence image sequences for neuron activity analysis traditionally relies on manual observation. To reduce labor costs, we cast this process as a novel one-shot active neuron localization task requiring minimal user intervention, i.e., only one active neuron template. Observing that neurons switch between active and inactive states over time, we formulate this task as a new one-shot multiple instance learning (MIL) problem, and propose an MIL-based framework integrating multifaceted properties. First, patch proposals are generated heuristically and combined into sequence proposals with temporal profile-based filtering. Second, a deep neural network is trained with self-supervision as the feature extractor. Third, the template feature and the patch feature of sequence proposals are extracted and compared to classify sequences and identify neuron positions in an MIL fashion. Experiments with in vivo data demonstrate our method's clear performance advantage over comparison methods, providing a foundation for future physiological analysis. The code is available at https://github.com/Spritea/OANL.
UR - https://www.scopus.com/pages/publications/105023716124
U2 - 10.1109/EMBC58623.2025.11254320
DO - 10.1109/EMBC58623.2025.11254320
M3 - Conference contribution
C2 - 41336714
AN - SCOPUS:105023716124
T3 - Proceedings of the Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBS
BT - 2025 47th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2025 - Proceedings
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 47th Annual International Conference of the IEEE Engineering in Medicine and Biology Society, EMBC 2025
Y2 - 14 July 2025 through 18 July 2025
ER -