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Abstract
Intracortical brain-computer interfaces (iBCIs) promise revolutionary clinical and research applications. State-of-the-art iBCIs rely on high-density (HD) microelectrode arrays (MEAs) to sense massive neuronal populations. However, HD MEAs are bandwidth-demanding, posing a significant challenge for wireless iBCIs. Prior iBCI systems have relied on compression to reduce neural signal bitrate. Unfortunately, existing schemes are blind to neurons’ signal characteristics, resulting in poor compression efficiency and severe degradation in iBCI performance.
This paper explores a neuron-aware approach to the design of efficient brain-to-computer communication systems. We present NeuroZip, a neural signal compression scheme that significantly reduces bitrate without compromising neural features, enabling various wireless iBCI applications to track neurons under limited bandwidth. To achieve this, NeuroZip first models and analyzes the complex feature space of HD neural signals, and then embraces neuron-awareness into an efficient genetic search algorithm that can quickly converge to an optimal compression strategy despite the large solution space yielded by HD MEA’s high microelectrode count. Preliminary experiments conducted on real neural datasets show that, compared to neuron-blind schemes, NeuroZip reduces bandwidth by up to 2.2x under the same error constraint, or reduces error rate by up to 8x under the same bandwidth. Further experiments demonstrate NeuroZip imposes minimal impacts on downstream iBCI tasks, limiting the increase of error rate within 2.4% for three representative iBCI applications.
© 2024 Copyright held by the owner/author(s).
This paper explores a neuron-aware approach to the design of efficient brain-to-computer communication systems. We present NeuroZip, a neural signal compression scheme that significantly reduces bitrate without compromising neural features, enabling various wireless iBCI applications to track neurons under limited bandwidth. To achieve this, NeuroZip first models and analyzes the complex feature space of HD neural signals, and then embraces neuron-awareness into an efficient genetic search algorithm that can quickly converge to an optimal compression strategy despite the large solution space yielded by HD MEA’s high microelectrode count. Preliminary experiments conducted on real neural datasets show that, compared to neuron-blind schemes, NeuroZip reduces bandwidth by up to 2.2x under the same error constraint, or reduces error rate by up to 8x under the same bandwidth. Further experiments demonstrate NeuroZip imposes minimal impacts on downstream iBCI tasks, limiting the increase of error rate within 2.4% for three representative iBCI applications.
© 2024 Copyright held by the owner/author(s).
Original language | English |
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Title of host publication | HOTMOBILE '24 |
Subtitle of host publication | Proceedings of the 25th International Workshop on Mobile Computing Systems and Applications |
Publisher | Association for Computing Machinery |
Pages | 107-113 |
ISBN (Print) | 979-8-4007-0497-0 |
DOIs | |
Publication status | Published - Feb 2024 |
Event | 25th International Workshop on Mobile Computing Systems and Applications, HOTMOBILE 2024 - San Diego, United States Duration: 28 Feb 2024 → 29 Feb 2024 |
Publication series
Name | HOTMOBILE - Proceedings of International Workshop on Mobile Computing Systems and Applications |
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Conference
Conference | 25th International Workshop on Mobile Computing Systems and Applications, HOTMOBILE 2024 |
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Country/Territory | United States |
City | San Diego |
Period | 28/02/24 → 29/02/24 |
Funding
We thank anonymous reviewers and our shepherd for their valuable feedback and constructive suggestions. This work is supported in part by Research Grants Council (RGC) of Hong Kong under General Research Fund No. 11204722.
Research Keywords
- Brain-computer interface
- neural signal compression
- spike sorting
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GRF: Tackling the Threat of Small Drones in Low Altitude Airspace over Metropolises
HUANG, J. (Principal Investigator / Project Coordinator) & Xing, G. (Co-Investigator)
1/01/23 → …
Project: Research