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Real-time, automatic, open-source sleep stage classification system using single EEG for mice


We developed a real-time sleep stage classification system with a convolutional neural network using only a one-channel electro-encephalogram source from mice and universally available features in any time-series data: raw signal, spectrum, and zeitgeber time. To accommodate historical information from each subject, we included a long short-term memory recurrent neural network in combination with the universal features. The resulting system (UTSN-L) achieved 90% overall accuracy and 81% multi-class Matthews Correlation Coefficient, with particularly high-quality judgements for rapid eye movement sleep (91% sensitivity and 98% specificity). This system can enable automatic real-time interventions during rapid eye movement sleep, which has been difficult due to its relatively low abundance and short duration. Further, it eliminates the need for ordinal pre-calibration, electromyogram recording, and manual classification and thus is scalable. The code is open-source with a graphical user interface and closed feedback loop capability, making it easily adaptable to a wide variety of end-user needs. By allowing large-scale, automatic, and real-time sleep stage-specific interventions, this system can aid further investigations of the functions of sleep and the development of new therapeutic strategies for sleep-related disorders.


The function of sleep has historically been investigated using sleep deprivation. Although this technique reveals the importance of sleep, it is difficult to establish causal relationships between sleep and observed phenotypes due to confounding factors accompanying sleep deprivation (e.g., stress). To avoid this issue, genetic methods were introduced to manipulate neural circuits that regulate sleep. However, these neural circuits are often hard-wired to those vital for other physiological processes (e.g., orexin neurons to appetite, melanin-concentrating hormone neurons to memory). Recently, optogenetics has revolutionized investigation into the function of sleep. Using optogenetics, target neuronal circuits can be specifically manipulated with light to interrogate their causal contributions during specific sleep stages while leaving sleep structure unchanged1,2,3. When using this technique, it is essential to classify a subject’s sleep stage in real-time for interrogation. However, a real-time, automatic, and scalable system for sleep stage classification for mice is lacking. Mice show a clear distinction between different sleep stages (i.e., rapid eye movement sleep (REM) and non-REM sleep (NREM)) and permit advanced genetic interventions. However, specifically examining the function of REM is difficult, mainly owing to its short and sparse nature (i.e., average ~ 1 min per episode, ~ fivefold less than NREM). Therefore, real-time, sensitive, and specific detection of REM in mice remains a challenge.

Real-time classification carries additional difficulties compared with offline classification, as parameters must be adjusted automatically for each subject, and artifacts and noise should be processed in real time. For example, Izawa et al. used a rule-based, real-time mouse sleep stage classification system2 in which thresholds are manually calibrated for each mouse before starting real-time classification, making it ill served for large-scale application. Furthermore, waveform patterns characteristic of each sleep stage (e.g., slow-wave activity, theta oscillations) are often defined by spectrum features using Fast Fourier Transformation (FFT). Indeed, Patanaik et al. developed a real-time human sleep classification system with a convolutional neural network (CNN) using FFT, but not raw, data from two-channel electroencephalogram (EEG) and two-channel electrooculogram4. They achieved 81.4% overall accuracy (ACC), 71.8% REM sensitivity, and 83.6% REM specificity. However, transformation of EEG waveform data to spectrum (i.e., FFT) data may lose transient wave characteristics that are potentially useful for stage classification. Most recently, Garcia-Molina et al. developed a system that classifies human sleep in real-time using one-channel EEG (1EEG)5. This system processes raw signals using a CNN with a long short-term memory network (LSTM) to incorporate historical information, which achieved Cohen's kappa values very close to those of professional judges and 72–94% REM specificity. However, a system that can robustly and automatically classify sleep stages in real time is still lacking.

Here, we report two fully automatic, real-time sleep stage classification systems for mice using 1EEG that use features common to any time-series data, which is unprecedented in existing systems. Our method is scalable and easily harnessed in any closed feedback loop system for real-time intervention in specific sleep stages, with especially high sensitivity and specificity for REM.


Development of a sleep stage classification system using universal time-series features

First, we developed a real-time sleep stage classification system with a CNN using 1EEG data from mice, named the universal time-series network (UTSN). UTSN processes raw EEG, FFT, and zeitgeber time (ZT) together. ZT is used because sleep is regulated by circadian rhythm6. The output from the CNN, FFT, and ZT are concatenated and transformed into a three-dimensional vector corresponding to the probabilities of each sleep stage (i.e., wakefulness, NREM, and REM) by a fully connected neural network (FCN) (Fig. 1). We did not use any de-noising preprocessor for the raw EEG signals, as the multi-layer architecture of the CNN can act as a set of filters and extract only meaningful information for sleep stage classification7.

Figure 1
figure 1

Network structure of the UTSN. Conv(\(a\),\({ }b\);\({ }c\)) indicates a block consisting of a one-dimensional convolution layer with kernel size \(a\) having \(b\) channels and stride set to \(c\). FC(\(d\)) is a block composed of a fully connected layer having \(d\) output channels. FFT, Fast Fourier Transformation; skip, skip-connection; ReLU, rectified linear unit; BN, batch normalization.

To make the UTSN applicable to closed feedback loop applications, we set the epoch window to 10 s, which was shown to be useful for optogenetic manipulation during REM3. For the activation function to nonlinearly transform the signal, we used a rectified linear unit (ReLU). Each convolution layer is followed by a ReLU activation layer and subsequent batch normalization (BN). BN standardizes the activity of each layer and prevents the vanishing gradient problem that occurs in deep learning. Two skip-connections8 are inserted to capture both crude and detailed characteristics. The 1–12 Hz range of the FFT spectrum, which covers the critical characteristic oscillatory activity in delta (1–4 Hz) and theta (6–9 Hz) bands, was split into 22 bins (i.e., 22-dimensional feature vector, 0.5 Hz per bin). We also implemented classifiers that use the short-time Fourier transform (STFT) instead of FFT, which resulted in marginal improvement (Suppl. Figs. 14, Suppl. Tables 57). As the task is multiclass classification, the softmax function converts the output of the FCN to a vector representing a probability distribution over sleep stages. Finally, the argmax function outputs the sleep stage with the highest estimated probability.

Addition of LSTM

We hypothesized that historical information would be useful for classification, as previously shown5,7. Therefore, we developed another system (UTSN-L) that connects to a LSTM after FCN output from the UTSN (Fig. 2), which enables the use of the output layer (i.e., before the softmax function) of the UTSN. LSTM is a sequence processing neural network that incorporates past states (i.e., epochs) into the classification of present states.

Figure 2
figure 2

UTSN-L architecture. The signal from each epoch is processed using the same architecture as the UTSN until the FCN (i.e., before the final softmax function). \(x_{t}\), \(x_{t - 1}\), … \(x_{t - m + 1}\) are EEG signals for epochs \(t\) to \(t - m + 1\), respectively. The output of the FCN is a sequence of low dimensional feature vectors, \(v_{t}\), \(v_{t - 1}\), … \(v_{t - m + 1}\), which is sent to the LSTM. \(\hat{y}_{t}\) is the final output that predicts the sleep stage for epoch \(t\). The diagram shows a case in which \(m = 3\) (\(m = 10\) in the real implementation).

Training, validation, and testing

We prepared 214 recordings (6 h per recording) with ground truth (i.e., human-scored) tags annotated by human experts. Of these, 192 recordings were used for training and validation of the systems, and 22 were used for testing. For each of the three sets of training and validation sessions, the 192 recordings were randomly split into a training dataset of 182 recordings and a validation dataset of 10 recordings. Thus, we obtained three classifiers (i.e., trained system) for the UTSN, UTSN-L, and other methods for comparison.

Evaluation of sleep stage classification

We evaluated the performance of the UTSN and UTSN-L for the three trained classifiers by comparison with conventional methods and network models that partially utilize universal features (Table 1). As simple conventional methods, we used logistic regression5,9, which usually performs well for small datasets, and random forest10,11,12 and AdaBoost13,14, which are ensemble-based methods that perform well for large datasets. Random forest is an ensemble method that combines the results of training numerous decision trees, and AdaBoost is an adaptive variant of boosting that aggregates outputs of weak learners. To evaluate the contribution of each universal feature, we compared simpler CNN models using each feature (i.e., raw EEG, FFT, or ZT) alone or in combination. Each recording consisted of > fivefold fewer REM epochs than NREM epochs or wakefulness. In this case, multiclass statistics may not reflect actual performance, especially for a class with low frequency (i.e., REM). Therefore, for evaluation criteria, we also used specificity, sensitivity, accuracy, precision, F1 score, and Matthews Correlation Coefficient (MCC). Overall, the UTSN-L performed better than the UTSN (Table 1). Although our system is capable of making predictions in real time, all experiments were conducted using already acquired, human-scored data to allow cross-comparisons among methods. To simulate real-time prediction conditions, the classifiers were not allowed to use future data to judge the target epoch. Moreover, as UTSN-L cannot make predictions unless 10 successive epochs are stored, we omitted the prediction results for the first nine epochs from all methods.

Table 1 Prediction performance from validation.

For further evaluation, we chose one trained classifier each for the UTSN and UTSN-L for testing based on ACC score. Overall, the test results were consistent with the validation results (Table 2, Suppl. Table 1, n = 22 recordings), which was also supported by tenfold cross-validation (Suppl. Figs. 14, Suppl. Tables 57). Sleep architectures showed similar results as ground truth (Fig. 3A). Although total sleep amounts were almost identical (Fig. 3B), the UTSN tended to detect more transitions between sleep stages as evidenced by more (Fig. 3C) and shorter (Fig. 3D) episodes. Power spectrum analysis showed almost identical results (Fig. 4), corroborating the waveform patterns of the identified epochs (examples in Suppl. Fig. 6 and VIDEO S1). In summary, these results indicate that including the LSTM together with the three universal features improves the quality of sleep stage classification.

Table 2 Confusion matrix analysis from testing.
Figure 3
figure 3

Sleep architecture analysis from testing. (A) Hypnogram, (BD) sleep architecture. W, wakefulness; N, NREM; R, REM; GT, ground truth; UN, UTSN; UL, UTSN-L; WN, wakefulness to NREM; WR, wakefulness to REM; SN, NREM to wakefulness; NR, NREM to REM; RW, REM to wakefulness; RN, REM to NREM. Data are shown as mean 95% confidence interval (n = 22 recordings).

Figure 4
figure 4

Power spectrum analysis from testing. Power was normalized by the total power (0.5–20 Hz) for each stage. Note the clear peaks within delta range (1–4 Hz) in NREM and theta range (6–9 Hz) in REM. W, wakefulness; N, NREM; R, REM; GT, ground truth; UN, UTSN; UL, UTSN-L; average from n = 22 recordings.

Implementation of a GUI

For practical use in experimental protocols without requiring programing skills, we developed a graphical user interface (GUI) that can run on any personal computer capable of running Python and a USB-based data acquisition system (Fig. 5, VIDEO S1). Using this GUI, classifications can also be performed offline using text-based signal data. As the GUI can output classification results in real-time for an Arduino device, it can be immediately implemented in a closed feedback loop system of choice (delay is 10 s due to the epoch window size). The source code is publicly available and thus can easily be customized for specific end-user needs.

Figure 5
figure 5

The GUI. Boxes in the upper row show normalized EEG raw signals (blue). Boxes in the bottom row show signals from an open channel (Ch2, green), which can be used for electromyogram (EMG), a motion sensor, an override signal, etc. Predicted stage for each epoch is presented above the corresponding EEG signal. Numbers with bold letters (i.e., 47–50) indicate past epochs (e.g., 10 s each) analyzed by the chosen network. In this case, UTSN-L analyzed epochs 1–50 and is currently analyzing epoch 51 (not predicted at the present moment). As an additional function, users can override the prediction to wakefulness (“W”) if the Ch2 signal crosses a threshold defined by the user, and the threshold for override can be changed manually using a scroll bar in the top-right corner (“Override threshold to W”). Users can also choose whether to normalize the Ch2 signal (“Ch2 mode”). Please see VIDEO S1.


Here, we report two real-time, fully automatic mouse sleep stage classification systems using only 1EEG. These systems achieved high sensitivity and specificity for REM and are robust, scalable, and adaptable. They use a 10-s time window, which allows them to be implemented in a closed feedback loop system for functional analysis during specific sleep stages3. The use of three universal time-series features allow the systems to be adapted for more detailed classification of sleep stages (e.g., high-theta and low-theta wakefulness15) from a variety of signal sources, even those from other species (e.g., humans) and brain areas (e.g., local field potentials in the hippocampus).

We believe that eliminating electromyogram (EMG) from the input markedly expands the system’s applications, particularly when they are applied to species in which reliable EMG is not easily obtained (e.g., reptiles16). Moreover, reducing the number of input channels bestows these systems with simplicity and thus scalability against a backdrop of reduced information. Indeed, although there have been attempts to use 1EEG for real-time classification5,17, to the best of our knowledge, there is no real-time classification system using 1EEG for mice achieving sensitivity and specificity for REM as high as the UTSN-L. Even with 1EEG, the UTSN-L achieved high-quality classification with a relatively small set of training data compared with previous networks (for example, 7), suggesting the robustness of the architecture.

One general difficulty in training systems for classifying sleep stages is that the amount of each sleep stage is imbalanced, with REM being particularly rare. In the future, this problem could be alleviated by using a loss function tailored for imbalanced data18,19. Another possibility is the use of an attention mechanism20. Often in sleep stage classification, human experts deliberately choose which part of the raw signal to focus on after observing the overall signal shape in an epoch. For example, if the overall amplitude of a signal is relatively small and consistent, human experts assume it could be REM and look for additional indicators (e.g., theta oscillation) to support their conclusion. In the future, an attention mechanism may be able to mimic such strategies.

In summary, we developed automatic, real-time sleep stage classification systems for mice using 1EEG input that provides high REM sensitivity and accuracy. These systems could potentially be used to analyze other time-series datasets. As they allow large-scale closed feedback loop applications, they can be employed to further investigate the functions of sleep.



All animal experiments were approved by the University of Tsukuba Institutional Animal Care and Use Committee. C57Bl6/J mice, which do not exhibit sleep–wake abnormalities, were maintained in a home cage (cylindrical Plexiglas cage: 21.9-cm diameter, 31.6-cm height) in an insulated chamber (45.7 × 50.8 × 85.4 cm), which was maintained at an ambient temperature of 23.5 ± 2.0 °C under a 12-h light/dark cycle (9 AM to 9 PM) with ad libitum access to food and water in accordance with institutional guidelines. The study was carried out in compliance with the ARRIVE guidelines.

Implantation of EEG and EMG electrodes

At nine weeks of age, mice were anesthetized with isoflurane and fixed in a stereotaxic frame (Stoelting, USA). The height of bregma and lambda were adjusted to be equal. EEG/EMG electrodes were placed as previously described3. Briefly, EEG electrodes were stainless steel recording screws (Biotex Inc.) implanted epidurally at AP + 1.5 mm and − 3 mm and ML − 1.5 mm and − 1.7 mm, respectively, and EMG electrodes were stainless steel Teflon-coated wires (AS633, Cooner Wire, USA) bilaterally placed into the trapezius muscles.

EEG and EMG recording

One week after electrode placement, mice underwent EEG and EMG recording in their home cage equipped with a data acquisition system capable of simultaneous video recording (Vital recorder, KISSEI COMTEC, Japan). Signals were recorded during ZT =  ~ 2 to 8 (~ 11 AM to 6 PM) for each mouse. Data were collected at a sampling rate of 128 Hz. Electric slip rings (Biotex Inc.) allowed mice to move and sleep naturally.

Sleep stage analysis by human experts

Sleep stage analysis by human experts was conducted based on visual characteristics of EEG and EMG waveforms with the help of FFT and video surveillance of mouse movement. The EEG dataset consisted of 214 recordings in total. In most cases, two recordings on two consecutive days were obtained from each mouse. Recordings were divided into 10-s epochs. FFT analysis was performed using Sleep Sign software (KISSEI COMTEC).

Wakefulness was defined by continuous mouse movement or de-synchronized low-amplitude EEG with tonic EMG activity. NREM was defined by dominant high-amplitude, low-frequency delta waves (1–4 Hz) accompanied by less EMG activity than that observed during wakefulness. REM was defined as dominant theta rhythm (6–9 Hz) and the absence of tonic muscle activity. If a 10-s epoch contained more than one sleep stage (i.e., NREM, REM, or wakefulness), the most represented stage was assigned for the epoch. At least two experts agreed on the classification of each recording.

Training, validation, and testing of UTSN and UTSN-L

To prepare the data for training, we normalized EEG data using the mean and standard deviation of all sample points in that recording. Let \(x_{\tau }\) be the observed value of EEG at a sample time point \(\tau\). In our experiment, the sampling frequency of EEG was 128 Hz, so t increments by 1/128 s. For validation and testing, we normalized EEG at each sample point (i.e., every 1/128 s) using the mean and standard deviation of all preceding values. In other words, for each sample point, the value was normalized as

$$\tilde{x}_{\tau } = \left( {x_{\tau } - \mu_{\tau } } \right)/\sigma_{\tau }$$


$$\mu_{\tau } = \frac{1}{\tau }\mathop \sum \limits_{s = 1}^{\tau } x_{s} \;{\text{and}}\;\sigma_{\tau }^{2} = \frac{1}{\tau }\mathop \sum \limits_{s = 1}^{\tau } \left( {x_{s} - \mu_{\tau } } \right)^{2} .$$

This process assimilates the real-time classification condition. On average, each recording consisted of ~ 2161 epochs.


The network structure and hyperparameters of the CNN and LSTM in the UTSN and UTSN-L were selected from various possible models through preliminary evaluation (Suppl. Tables 23).

Neural network architecture

A one-dimensional convolutional neural network processes the raw EEG data.

As the sampling rate is 128 Hz and the time window is 10 s, the segment is a 1280-dimensional vector. This network consists of stacked convolution layers that aggregate values of spatially neighboring nodes and output a lower-dimensional representation. Each convolution layer consists of one or more kernels (or filters) that act as local feature detectors. Let \({\varvec{z}}\) be the input vector to a \(d\)-diensional kernel \({\varvec{\kappa}}\). The output of a convolution layer is a vector \({\varvec{a}}\) whose components are obtained by \(a_{\tau } = \mathop \sum \nolimits_{s = 1}^{d} \kappa_{s} z_{\tau - d + s}\).

Model evaluation

Models were evaluated by criteria commonly used for multiclass and binary classification tasks (Suppl. Table 4).

Statistical analysis

Statistical analysis was performed using GraphPad Prism version 7.04 for Windows (GraphPad Software, USA). Type I error was set at 0.05. Shapiro–Wilk tests were performed to assess the normality of data. Brown-Forsythe tests were performed to assess homogeneity of variance.

Software implementation

We implemented the system using PyTorch. The neural network models were trained using NVIDIA Quadro RTX 8000 with 48 GB memory.

Data availability

Data underlying the results described in this manuscript are available at (for reviewing only). (after acceptance) except for the raw EEG and EMG recording data with stage labels, which are available at

Code availability

Code for UTSN and UTSN-L are available at

Materials availability

No special materials were created in this study.


  1. Boyce, R., Glasgow, S. D., Williams, S. & Adamantidis, A. Causal evidence for the role of REM sleep theta rhythm in contextual memory consolidation. Science 352, 812–816 (2016).

    ADS  CAS  Article  Google Scholar 

  2. Izawa, S. et al. REM sleep–active MCH neurons are involved in forgetting hippocampus-dependent memories. Science 1313, 1308–1313 (2019).

    ADS  Article  Google Scholar 

  3. Kumar, D. et al. Sparse activity of hippocampal adult-born neurons during REM sleep is necessary for memory consolidation. Neuron 107, 552–565 (2020).

    CAS  Article  Google Scholar 

  4. Patanaik, A., Ong, J. L., Gooley, J. J., Ancoli-Israel, S. & Chee, M. W. L. An end-to-end framework for real-time automatic sleep stage classification. Sleep 41, 1–11 (2018).

    Article  Google Scholar 

  5. Bresch, E., Großekathöfer, U. & Garcia-Molina, G. Recurrent deep neural networks for real-time sleep stage classification from single channel EEG. Front. Comput. Neurosci. 12, 1–12 (2018).

    Article  Google Scholar 

  6. Szymanski, J. S. Die Verteilung der Ruhe- und Aktivitätsperioden bei weissen Ratten und Tanzmäusen. Pflüger’s Arch. für die gesamte Physiol. des Menschen und der Tiere 171, 324–347 (1918).

    Article  Google Scholar 

  7. Yamabe, M. et al. MC-SleepNet: large-scale sleep stage scoring in mice by deep neural networks. Sci. Rep. 9, 1–12 (2019).

    CAS  Article  Google Scholar 

  8. He, K., Zhang, X., Ren, S. & Sun, J. Deep residual learning for image recognition. In Proceedings of the IEEE Computer Society Conference on Computer Vision and Pattern Recognition 2016-Decem, 770–778 (2016).

  9. Biswal, S. et al. SLEEPNET: automated sleep staging system via deep learning. arXiv:1707.08262 [cs.LG] (2017).

  10. Fraiwan, L., Lweesy, K., Khasawneh, N., Wenz, H. & Dickhaus, H. Automated sleep stage identification system based on time-frequency analysis of a single EEG channel and random forest classifier. Comput. Methods Programs Biomed. 108, 10–19 (2012).

    Article  Google Scholar 

  11. Memar, P. & Faradji, F. A novel multi-class EEG-based sleep stage classification system. IEEE Trans. Neural Syst. Rehabil. Eng. 26, 84–95 (2018).

    Article  Google Scholar 

  12. Walch, O., Huang, Y., Forger, D. & Goldstein, C. Sleep stage prediction with raw acceleration and photoplethysmography heart rate data derived from a consumer wearable device. Sleep 42, 1–19 (2019).

    Google Scholar 

  13. Hassan, A. R. & Hassan Bhuiyan, M. I. Automatic sleep scoring using statistical features in the EMD domain and ensemble methods. Biocybern. Biomed. Eng. 36, 248–255 (2016).

    Article  Google Scholar 

  14. Ilhan, H. O. Sleep stage classification via ensemble and conventional machine learning methods using single channel EEG signals. Int. J. Intell. Syst. Appl. Eng. 4, 174–184 (2017).

    Article  Google Scholar 

  15. Buzsáki, G. Theta oscillations in the hippocampus. Neuron 33, 325–340 (2002).

    Article  Google Scholar 

  16. Norimoto, H. et al. A claustrum in reptiles and its role in slow-wave sleep. Nature 578, 413–418 (2020).

    ADS  CAS  Article  Google Scholar 

  17. Garcia-Molina, G. et al. Hybrid in-phase and continuous auditory stimulation significantly enhances slow wave activity during sleep. In Proc. Annu. Int. Conf. IEEE Eng. Med. Biol. Soc. EMBS 4052–4055 (2019). doi:

  18. GoodSmith, D. et al. Spatial representations of granule cells and mossy cells of the dentate gyrus. Neuron 93, 677-690.e5 (2017).

    CAS  Article  Google Scholar 

  19. Mousavi, S., Afghah, F. & Rajendra Acharya, U. Sleepeegnet: automated sleep stage scoring with sequence to sequence deep learning approach. PLoS ONE 14, 1–15 (2019).

    Google Scholar 

  20. Bahdanau, D., Cho, K. H. & Bengio, Y. Neural machine translation by jointly learning to align and translate. In 3rd Int. Conf. Learn. Represent. ICLR 2015—Conf. Track Proc. 1–15 (2015).

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We thank Dr. Katherine Akers for critical comments on the manuscript; Ms. Pimpimon Nondhalee, Mr. Kengo Shikama, Mr. Yuzuki Mimura, Mr. Takuma Hosokawa, Mr. Makoto Hiramatsu, Mr. Takashi Mikami, Mr. Akinobu Ohba, Mr. Natsu Hasegawa, and Mr. Pablo Vergara for their technical assistance; and Ms. Mari Sakurai for secretarial support. This work was partially supported by grants from the World Premier International Research Center Initiative from MEXT; JST CREST grant #JPMJCR1655; JSPS KAKENHI Grants #16K18359, 15F15408, 26115502, 25116530, JP16H06280, 19F19310, and 20H03552; Shimadzu Science Foundation; Takeda Science Foundation; Kanae Foundation; Research Foundation for Opto-Science and Technology; Ichiro Kanehara Foundation; Kato Memorial Bioscience Foundation; Japan Foundation for Applied Enzymology; Senshin Medical Research Foundation; Life Science Foundation of Japan; Uehara Memorial Foundation; Brain Science Foundation; Kowa Life Science Foundation; Inamori Research Grants Program; and GSK Japan to M.S, and JSPS KAKENHI Grant #18KK0308 and G7 Scholarship Foundation to TT.

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Conceptualization, M.S. and T.T.; Methodology, T.T., D.K., S.S., I.K., and M.S.; Investigation, T.T., D.K., S.S., I.K., and T.N.; Validation, T.T. and D.K.; Formal Analysis, T.T.; Data Curation, T.T. and M.S.; Visualization, T.T.; Writing—Original Draft, T.T.; Writing—Review and Editing, T.T., M.S., and I.K.; Funding Acquisition, T.T. and M.S.; Resources, T.T. and M.S.; Supervision, T.T. and M.S.; Project Administration, T.T. and M.S. All authors discussed and approved the manuscript.

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Correspondence to Taro Tezuka or Masanori Sakaguchi.

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Tezuka, T., Kumar, D., Singh, S. et al. Real-time, automatic, open-source sleep stage classification system using single EEG for mice. Sci Rep 11, 11151 (2021).

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