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Peer-reviewedCC BYNPJ digital medicine

AnySleep: a channel-agnostic deep learning system for high-resolution sleep staging in multi-center cohorts.

8 affiliations
  1. 1Department of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Jülich, Germany. [email protected].
  2. 2Department of Information and Computing Sciences, Utrecht University, Utrecht, The Netherlands. [email protected].
  3. 3Institute for Data-Driven Technologies, FH Aachen University of Applied Sciences, Jülich, Germany. [email protected].
  4. 4Department of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Jülich, Germany.
  5. 5Institute for Data-Driven Technologies, FH Aachen University of Applied Sciences, Jülich, Germany.
  6. 6Department of Information and Computing Sciences, Utrecht University, Utrecht, The Netherlands.
  7. 7Department of Medical Engineering and Technomathematics, FH Aachen University of Applied Sciences, Jülich, Germany. [email protected].
  8. 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  -