Sleep stage classification, including wakefulness (W), rapid eye movement (REM), and nonrapid eye movement (NREM) which includes three sleep stages that describe the depth of sleep, is one of the most critical steps in effective diagnosis and treatment of sleep-related disorders. Clinically, sleep staging is performed by domain experts through visual inspection of polysomnography (PSG) recordings, which is time-consuming, labor-intensive and often subjective in nature. Therefore, this study develops an automatic sleep staging system, which uses single channel electroencephalogram (EEG) signal, for convenience of wearing and less interference in the sleep, to do automatic identification of various sleep stages. To achieve the automatic sleep staging system, this study proposes a two-layer stacked ensemble model, which combines the advantages of random forest (RF) and LightGBM (LGB), where RF focuses on reducing the variance of the proposed model while LGB focuses on reducing the bias of the proposed model. Particularly, the proposed model introduces a class balance strategy to improve the N1 stage recognition rate. In order to evaluate the performance of the proposed model, experiments are performed on two datasets, including Sleep-EDF database (SEDFDB) and Sleep-EDF Expanded database (SEDFEDB). In the SEDFDB, the overall accuracy (ACC), weight F1-score (WF1), Cohen's Kappa coefficient (Kappa), sensitivity of N1 (SEN-N1) obtained by proposed model are 91.2%, 0.916, 0.864 and 72.52% respectively using subject-non-independent test (SNT). In parallel, the ACC, WF1, Kappa, SEN-N1 obtained by proposed model are 82.4%, 0.751, 0.719 and 27.15% respectively using subject-independent test (SIT). Experimental results show that the performance of the proposed model are competitive with the state-of-the-art methods and results, and the recognition rate of N1 stage is significantly improved. Moreover, in the SEDFEDB, the experimental results indicate the robustness and generality of the proposed model. INDEX TERMS Sleep stage classification, single channel EEG signal, two-layer stacked ensemble model, random forest, LightGBM.
Background: Hepatitis B (HepB) vaccination can effectively prevent the prevalence of hepatitis B virus (HBV) infection. However, the incidence of vaccination failure is about 5~10% and the underlying molecular mechanisms are poorly understood. T cells have an essential role in the recipient's immune response to vaccine, which could be elucidated by high-throughput sequencing (HTS) and bioinformatics analysis. Methods: We conducted HTS of the T cell receptor β chain (TRB) complementarity-determining region 3 (CDR3) repertoires in eighteen positive responders (responders) and 10 negative responders (non-responders) who all had HepB vaccination, the repertoire features of BV, BJ and V-J genes and their diversity, respectively, were compared between the positive and negative responders using the Mann-Whitney test. Moreover, the relatively conserved motifs in CDR3 were revealed and compared to those in the other group's report. Results:The diversity of TRB CDR3 and the frequencies of BV27 and BV7-9 are significantly increased for HepB vaccine responders compared to those in non-responders. The motifs of CDR3s in BV27/J1-1, BV27/J2-5, and BV7-9/J2-5, respectively, were most expressed as "NTE", "QETQ", and "GG-Q (E)-ETQ". Moreover, the motif "KLNSPL" was determined in nearly 80% CDR3s in BV27/J1-6 from HepB vaccine responders for the first time. Conclusion: Our results present the comprehensive profiles of TRB CDR3 in the HepB vaccine responders and non-responders after standard vaccination protocol and determine the relatively conservative motifs of CDR3s that may respond to the HepB vaccine. Further results suggest that the profile of TRB repertoire could distinguish the HepB vaccine responders from non-responders and provide a new target for optimizing and improving the efficiency of the HepB vaccine.
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