AnySleep: a channel-agnostic deep learning system for high-resolution sleep staging in multi-center cohorts.
8 affiliations
- 1Department of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Jülich, Germany. [email protected].
- 2Department of Information and Computing Sciences, Utrecht University, Utrecht, The Netherlands. [email protected].
- 3Institute for Data-Driven Technologies, FH Aachen University of Applied Sciences, Jülich, Germany. [email protected].
- 4Department of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Jülich, Germany.
- 5Institute for Data-Driven Technologies, FH Aachen University of Applied Sciences, Jülich, Germany.
- 6Department of Information and Computing Sciences, Utrecht University, Utrecht, The Netherlands.
- 7Department of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Jülich, Germany. [email protected].
- 8Institute for Data-Driven Technologies, FH Aachen University of Applied Sciences, Jülich, Germany. [email protected].
Abstract
Sleep is essential for health, yet studying its dynamics requires manual sleep staging, a labor-intensive step in research and clinical care. Across centers, polysomnography (PSG) recordings are traditionally scored in 30-s epochs for pragmatic, not physiological, reasons and vary in electrode count, montage, and subject characteristics. These constraints challenge harmonized multi-center studies and the discovery of robust biomarkers on shorter timescales. We present AnySleep, a deep neural network that scores sleep from any electroencephalography (EEG) or electrooculography (EOG) data at adjustable temporal resolutions. We trained and validated the model on over 20,000 overnight recordings (>200,000 h of EEG and EOG) from 28 datasets across multiple clinics to promote robust generalization across sites. The model attains state-of-the-art performance and surpasses or equals established baselines at 30-s epochs. Performance improves with more channels, yet remains strong when EOG is absent, or only EOG or single EEG derivations (frontal, central, or occipital) are available. On sub-30-s timescales, the model captures short wake intrusions consistent with arousals and improves the prediction of pathophysiological conditions (obstructive sleep apnea, narcolepsy type 1, insomnia) over 30-s scoring. We make the model publicly available to facilitate large-scale studies with heterogeneous electrode setups and accelerate biomarker discovery in sleep.
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BibTeX
@article{grieger2026anysleep,
title = {{AnySleep: a channel-agnostic deep learning system for high-resolution sleep staging in multi-center cohorts.}},
author = {Niklas Grieger and Jannik Raskob and Siamak Mehrkanoon and Stephan Bialonski},
journal = {NPJ digital medicine},
year = {2026},
month = oct,
doi = {10.1038/s41746-026-03406-7},
url = {https://europepmc.org/article/MED/42963354},
note = {CC BY},
}
RIS
TY - JOUR
TI - AnySleep: a channel-agnostic deep learning system for high-resolution sleep staging in multi-center cohorts.
AU - Niklas Grieger
AU - Jannik Raskob
AU - Siamak Mehrkanoon
AU - Stephan Bialonski
PY - 2026
DA - 2026/10/30
JO - NPJ digital medicine
DO - 10.1038/s41746-026-03406-7
UR - https://europepmc.org/article/MED/42963354
AB - Sleep is essential for health, yet studying its dynamics requires manual sleep staging, a labor-intensive step in research and clinical care. Across centers, polysomnography (PSG) recordings are traditionally scored in 30-s epochs for pragmatic, not physiological, reasons and vary in electrode count, montage, and subject characteristics. These constraints challenge harmonized multi-center studies and the discovery of robust biomarkers on shorter timescales. We present AnySleep, a deep neural network that scores sleep from any electroencephalography (EEG) or electrooculography (EOG) data at adjustable temporal resolutions. We trained and validated the model on over 20,000 overnight recordings (>200,000 h of EEG and EOG) from 28 datasets across multiple clinics to promote robust generalization across sites. The model attains state-of-the-art performance and surpasses or equals established baselines at 30-s epochs. Performance improves with more channels, yet remains strong when EOG is absent, or only EOG or single EEG derivations (frontal, central, or occipital) are available. On sub-30-s timescales, the model captures short wake intrusions consistent with arousals and improves the prediction of pathophysiological conditions (obstructive sleep apnea, narcolepsy type 1, insomnia) over 30-s scoring. We make the model publicly available to facilitate large-scale studies with heterogeneous electrode setups and accelerate biomarker discovery in sleep.
SN - 2398-6352
ER -