The polysomnogram (PSG) is the gold standard for evaluating sleep quality and disorders. Attempts to automate this process have been hampered by the complexity of the PSG signals and heterogeneity among subjects and recording hardwares. Most of the existing methods for automatic sleep stage scoring rely on hand-engineered features that require prior knowledge of sleep analysis. This paper presents an end-to-end deep transfer learning framework for automatic feature extraction and sleep stage scoring based on a single-channel EEG. The proposed framework was evaluated over the three primary signals recommended by the American Academy of Sleep Medicine (C4-M1, F4-M1, O2-M1) from two data sets that have different properties and are recorded with different hardware. Different Time-Frequency (TF) imaging approaches were evaluated to generate TF representations for the 30 s EEG sleep epochs, eliminating the need for complex EEG signal pre-processing or manual feature extraction. Several training and detection scenarios were investigated using transfer learning of convolutional neural networks (CNN) and combined with recurrent neural networks. Generating TF images from continuous wavelet transform along with a deep transfer architecture composed of a pre-trained GoogLeNet CNN followed by a bidirectional long short-term memory (BiLSTM) network showed the best scoring performance among all tested scenarios. Using 20-fold cross-validation applied on the C4-M1 channel, the proposed framework achieved an average per-class accuracy of 91.2%, sensitivity of 77%, specificity of 94.1%, and precision of 75.9%. Our results demonstrate that without changing the model architecture and the training algorithm, our model could be applied to different single-channel EEGs from different data sets. Most importantly, the proposed system receives a single EEG epoch as an input at a time and produces a single corresponding output label, making it suitable for real time monitoring outside sleep labs as well as to help sleep lab specialists arrive at a more accurate diagnoses.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693852PMC
http://dx.doi.org/10.3390/s22228826DOI Listing

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