Next Article in Journal
Heart Rate Variability by Dynamical Patterns in Windows of Holter Electrocardiograms: A Method to Discern Left Ventricular Hypertrophy in Heart Transplant Patients Shortly after the Transplant
Next Article in Special Issue
AlphaFold2 Update and Perspectives
Previous Article in Journal
Modeling the Double Peak Phenomenon in Drug Absorption Kinetics: The Case of Amisulpride
Previous Article in Special Issue
Ablefit: Development of an Advanced System for Rehabilitation
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Systematic Review

A Systematic Review of Machine Learning Models in Mental Health Analysis Based on Multi-Channel Multi-Modal Biometric Signals

Industrial and Systems Engineering, Mississippi State University, Starkville, MS 39762, USA
*
Authors to whom correspondence should be addressed.
BioMedInformatics 2023, 3(1), 193-219; https://doi.org/10.3390/biomedinformatics3010014
Submission received: 17 January 2023 / Revised: 22 February 2023 / Accepted: 22 February 2023 / Published: 1 March 2023

Abstract

:
With the increase in biosensors and data collection devices in the healthcare industry, artificial intelligence and machine learning have attracted much attention in recent years. In this study, we offered a comprehensive review of the current trends and the state-of-the-art in mental health analysis as well as the application of machine-learning techniques for analyzing multi-variate/multi-channel multi-modal biometric signals.This study reviewed the predominant mental-health-related biosensors, including polysomnography (PSG), electroencephalogram (EEG), electro-oculogram (EOG), electromyogram (EMG), and electrocardiogram (ECG). We also described the processes used for data acquisition, data-cleaning, feature extraction, machine-learning modeling, and performance evaluation. This review showed that support-vector-machine and deep-learning techniques have been well studied, to date.After reviewing over 200 papers, we also discussed the current challenges and opportunities in this field.

1. Introduction

It is a bitter pill to swallow: At least one-in-five adults suffers from at least one form of mental health issue or disorder.These health conditions involve changes in emotions, thinking, behavior, or a combination of these [1], such as attention-deficit/hyperactivity disorder (ADHD), sleep apnea disorder, and depression [2,3,4,5,6]. Mental health issues affect well-being, impairing relationships and cognitive activities and causing body responses that may place individuals at risk.
A significant amount of research has leveraged the application of machine learning (ML) techniques for extracting, detecting, and classifying mental health biomarkers in sensor datasets [7,8,9,10,11,12]. These biosensor data are usually multi-channel, and even multi-modal, time series [13]. In the medical field, two types of signals are commonly collected for diagnosis, which includes bio-electric and non-bio-electric signals. These signals typically require expert evaluation to make a valid diagnosis [14]. With the assistance of ML techniques, there is the potential to increase the efficiency of mental health diagnosis and even the prognoses of mental disorders at an early stage, given the widely monitored signals through wearable devices in recent years. Biological signals can be collected through different modalities. For example, in this paper, we reviewed the application of ML techniques for electroencephalograms (EEGs), which records signals from the brain [15]; electro-oculograms (EOGs), which record the movement signals of the eyes [16]; electromyograms (EMGs), which record signals from muscle activities during sleep stages [17,18,19]; and electrocardiograms (ECGs), which record signals from the heart via a heart-rate monitor. Non-bio-electric signals include body temperature, respiration, and blood pressure. Despite there being many biological signals for diagnosing mental diseases, this work concentrated on bio-electrical signals and ML techniques that have been used to promote the diagnosis of mental health issues [20].
There are various biological signal types [21]: bio-electrical signals, bio-acoustic signals, bio-mechanical signals, bio-chemical signals, and body temperature. Bio-electrical signals occur in the body of cells, and they originate from the electric activities occurring in the body. These signals have been used for diagnosing various diseases using ML techniques, which is a subset of artificial intelligence (AI) methodologies. In this work, we reviewed the trends and the state-of-the-art of these ML techniques for mental health diagnosis, and we investigated the methods by which these signals are used to increase the efficiency of diagnosing mental health diseases.These bio-electric signals are collected through electrodes and specialty devices. In sleep medicine, large datasets have been generated with these devices to assist in characterizing and quantifying sleep and sleep-related disorders [22]. Polysomnography (PSG) data [23] have been the most commonly used test for the diagnosis of obstructive sleep apnea syndrome (OSAS) and other related ailments. PSG procedures have been conducted primarily overnight in a sleep laboratory. To effectively diagnose sleep disorders, PSG records have been used, collected, and scored by experts [24,25,26,27]. PSG records are data extracted from brain-wave recordings, oxygen levels, heart rate monitors, breathing rates, as well as leg and eye movements of patients.EEG, EOG, EMG, and ECG signals as well as sleep videos have also been integrated into PSGs [17,23,24,25,28]. It has been estimated by World Health Organization (WHO) that nearly one-third of the world population suffers from sleep disorders [29]. PSG analysis has been defined as the gold standard for detecting sleep disorders and other mental health diseases [30]. PSG records are multi-signal channels. For sleep studies and scoring, an expert is often required to manually examine PSG records. Therefore, the results are at risk of human error, and it is time-consuming and expensive to carry out [31].
Collecting PSG data can be very expensive and uncomfortable for the patient; therefore, it is vital to ensure an accurate diagnosis based on this test’s results [32,33,34,35].The traditional PSG process requires the measuring of EEG, EOG, EMG, and ECG signals [28]. A significant amount of research has employed deep-learning approaches to model the spatio-temporal aspects of PSG data [24]. Later in this paper, we reviewed the advantages of ML in a study of mental health diseases. Since 1970, there have been improvements in the automatic scoring of PSG records, in accordance to Rechtschaffen and Kales (RK) sleep research [33,36] based on the American Academy of Sleep Medicine (AASM) rules [37]. The visual interpretations of the PSG signals of patients have been a widely accepted approach for analyzing sleep stages and mental-health-related diseases [38]. In many countries, PSG technology and experts in sleep study have been limited, however, so there is an urgent need to achieve automated PSG data analysis with the help of AI techniques [39].
Sleep recordings require the measurement of brain activity (EEG), eye movement (EOG), and muscle activity (EMG) to accurately identify specific sleep stages. EEGs have been intensely researched by many scholars. EEG signals are classified by employing a common spatial pattern (CSP) and differential entropy (DE) characteristics to the delta, theta, alpha, beta, and gamma frequency bands [40,41]. The diagnosis of mental health and sleep disorders can be tedious and requires significant time investment and expertise to obtain a reliable and accurate diagnosis. In many cases, patients have been subjected to prolonged interviews to improve the diagnostic accuracy of the health personnel or expert [41]. With an EEG system, some limitations have been overcome, and the process of feature extraction, classification, and prediction for the diagnosis of mental health diseases based on PSG datasets could potentially be automated using ML techniques.
Among other signal types, EEGs have been a focus of much study for mental health diagnosis by many researchers. However, there are significantly fewer articles on other biological signals, such as EMG, EOG, and ECG. The study in [42] presented a comprehensive survey of ECG signals, and the authors concluded that a significant amount of studies will be published on ECG in the near future. The study in [43] showed that HRV analysis was a viable method for feature extraction from ECG signals. The researchers in [44] proposed and evaluated an automated analysis of single-lead ECG analyses using human recognition patterns.EMGs have different statistical and spectral properties from the other signals [25]. EMG signals have been used as a bio-signal for hand-and-wrist-gesture recognition [45]. PSG data provide comprehensive information for sleep studies and sleep disorder diagnosis.
It has been estimated that at least 2–4 percent of adults and 1–3 percent of children suffer from sleep-related ailments [31]. There are many classifications that have been used for determining sleep stages. The application of ML and AI has assisted scientists and health professionals in recent times to improve the accuracy of sleep-stage classification and mental health diseases [46]. Combrisson et al. [47] implemented several algorithms for the automatic detection of sleep features and embedded them within a software platform, which they referred to as “detection” panels.
PSG records have been broken into 30s epochs, which were then classified as different sleep stages by experts [48], based on the AASM and Rechtschaffen and Kales sleep classification recommendations [29,48,49]. Sleep has been classified into periods of rapid eye movement (REM) and non-rapid eye movement (NREM), including Stage W (wakefulness), Stage N1 (NREM 1), Stage N2 (NREM 2), Stage N3/N4 (NREM 3), and Stage R (REM) [22,24,25,32,50]. Many studies have identified EEG signals as a more effective bio-electric signal for sleep classification [51] and for the diagnosis of other mental health diseases, such as depression and ADHD [35,52]. Figure 1 [29,38] shows a schematic flowchart of sleep-stage classification with PSG signals from bio-electric signals, specifically EEG. We classified sleep as light sleep and deep sleep, and the wavelength shown in Figure 1 is a typical wave pattern for EGG signals [53]. Each sleep stage can be distinguished based on the wavelengths.
In this work, we reviewed the application of ML techniques on multi-modal and multi-channel PSG datasets. This work aimed to provide researchers with information on the current trends related to the application of ML for bio-electrical signals.The rest of this paper is structured as follows: First, a background section with a subsection details the method of article selection. Secondly, a section illustrates the methods of applying ML techniques on multi-modal and multi-channel PSG datasets. This section has multiple subsections, including data acquisition, data preparation, feature extraction, balancing datasets, ML techniques, and performance evaluation. Thirdly, a summary and discussion section is presented. Finally, this study is concluded, and some recommendations are discussed.

2. Background and Prior Work

2.1. Literature Search Process

For this review, we carried out keyword searches on specific literature databases. The keywords used for this literature search were based on the goal of this study. The keywords used for this search were as follows: (“EEG” OR “ECG” OR “EOG” OR “EMG” OR “PSG”) AND “Machine Learning” AND “Mental Health”. This search was carried out on commonly used databases, such as Science Direct, IEEE Xplore, MDPI, and PubMed. The search criteria used for obtaining literature for this work are summarized, as follows:
  • Publications had to be released in 2017 or later.
  • To deepen the understanding of the research questions, we also added 25 articles published between the years 2000 and 2016. This range was selected based on references from similar research.
  • Articles had to have at least one or more of the keywords.
  • Articles had to be published in recognized literature databases/websites.
  • All selected papers had to be written in English.
  • All papers were either studies, surveys, or reviews of the application of ML on PSG data and the classification of mental health issues using ML.
Table 1 shows the digital-database advanced search strings used to collect articles for this review. Using the following search criteria (“EEG” OR “ECG” OR “EOG” OR “EMG” OR “PSG”) AND “Machine Learning” AND “Mental Health”, which consisted of commonly used boolean operators [1,54], i.e., AND (must be included in the search) as well as OR (may or may not be included in the search), 1074 article were identified, and they were further screened for inclusion in this work.
Figure 2 shows The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) for article search and collections for our review. Using PRISMA 2020 statements and guidelines, a checklist was used to structure this systematic review and avoid biases during article selection. PRISMA was designed in 2009 [55] to address poor or weak reporting of systematic reviews, and it also assisted in structuring a review in order to provide useful value for the readers of systematic reviews. This study was also registered in INPLASY, which is an international platform of registered systematic review and meta-analysis protocols. Many existing review articles studied in this systematic review also used the PRISMA statement and guidelines [32,54,56,57,58,59,60]. This work leveraged prior research from different authors to perform a detailed review of the applications of ML on multi-channel and multi-modal PSG data.
In this work, we included 218 papers that met our criteria and were related to our research questions in terms of material presentation, methods, and results, as shown in the PRISMA flow diagram in Figure 2. Records were screened and reviewed against the quality of work conducted in the studies and its relevance to our research goal.

2.2. Word-Cloud Overview

Word clouds and bar graphs were created based on the titles and abstracts of all the articles reviewed [61]. Figure 3 shows a word cloud and bar graph of all the titles of the articles reviewed for this work. The most frequent words, as shown by the word cloud, were learning, EEG, sleep, machine, detection, and anomaly, among others, and Figure 4 shows a word cloud and the 30 most frequent words used in the abstracts from all the articles reviewed in this paper. The most frequent words used in the abstracts were similar to those used in the full-text articles, but with more weight on words such as data, model, and so on.This showed that the collected articles aligned with the main goal of this study. Furthermore, most of the sleep studies were related to the use of EEG signals and considered the problem as a time-series anomaly detection problem.

2.3. Literature Distribution by Publication Year

Figure 5 is a summary of the number of articles reviewed in this paper, grouped by publication year, with 55 and 43 articles published in 2022 and 2021, respectively. We focused on recent research that had been carried out by researchers in this field.

2.4. Methods

In this section, Figure 6 shows a process flow of deploying ML on PSG datasets. We considered the details of each individual block, as shown in Figure 6. Each block shows how the PSG data were prepared [62], extracted, processed, and classified for disease diagnosis, step by step. A similar approach was also used by Sekkal et al. [63].

2.4.1. Data Preparation

The methodologies of processing PSG signal-processing have been divided into four stages [67]: data acquisition, pre-processing, feature extraction, and classification. PSG data have become the most prevalent records used for studies that apply ML for mental health diagnosis and classification, and there were many open-access datasets that had been generated by previous research. In this review, we summarized some of the available datasets and the papers they used. We identified three predominant resources that provided open access to PSG data.
  • An official website (https://sleepdata.org/; accessed on 21 February 2023) managed by The National Sleep Research Resource, provides open access for researchers and those interested in sleep studies, with large collections of physiological signals and clinical data elements. These datasets were collected from structured research cohorts and clinical trials. The Nationwide Children’s Hospital (NCH) Sleep Data Bank consisted of three folders: Sleep Data, Health Data, and the Sleep Data with annotated PSG data recordings [68].
  • The Montreal Archive of Sleep Studies (MASS) (http://ceams-carsm.ca/en/MASS/; accessed on 21 February 2023) is an open-access and collaborative database of laboratory-based PSG recordings. It also comprised a cohort of subsets [25,69].
  • PhysioNet (https://physionet.org/; accessed on 21 February 2023) is an open-access physiologic-signal data source that is managed by members of the MIT Laboratory for Computational Physiology [68,70,71].
Table 2 summarizes the commonly used open-access PSG datasets. Khosla et al. and Engemann et al. [72,73,74] have more detailed lists of PSG/EEG datasets.

2.4.2. Data Acquisition

For a typical sleep study, at least a one-night PSG test was required per subject for data collection [37,90,91,92]. With the assistance of expert interviews, the data were determined. All raw PSG datasets were stored in the European data format (EDF). Devices/sensors were always attached to the body of the subject overnight to collect data [41,42,93]. The key characteristics of a good dataset were the following: It had an appropriate sampling frequency in Hz with multiple channels and a reference electrode. The source of the dataset was also necessary to ensure researchers could reference the datasets in their works. The collected datasets had to be large in size and heterogeneous in nature. Most EGG dataset used 19 or 16 channels [67,94], i.e., (F3, F4, T3, T4, C3, C4, P3, P4, FZ, CZ, PZ, Fp1, Fp2, F7, F8, T5, T6), and (O1, O2) [67,74]. Notations including F, T, C, P, and O denoted frontal, temporal, central, parietal, and occipital, respectively, which were used to identify the brain lobes and placements of the electrodes on the scalp surface [14,21,54]. Figure 7 shows the various locations of electrode placement for electroencephalogram (EEG) data collection using a 10–20 scalp electrode system [14,95] for capturing EEG signals. The scalp electrodes were used to record brain activities via EEG signals. This was recorded by an electroencephalograph. In clinical practice, a standard ECG signal was obtained using 10 electrodes (4 limb and 6 thorax electrodes) [21,96]. All these bio-signals included noise that originated from the patient’s body and the environment. Moreover, noise caused distortions in the time and frequency of the signals. A filtering process is typically required to eliminate these noises, which is known as pre-processing [97]. Most existing sleep studies considered EEG signals the predominant PSG signals for the diagnosis. These are brain wave signals collected at a sampling frequency.

2.4.3. Pre-Processing of Signals

For feature extraction, all acquired signal needed to be pre-processed by setting up a frequency threshold. It is common practice to set the EEG signal at 100  ( μ ν ) . Signals above this threshold are then considered to be noise [95,98]. Figure 8 shows the step for pre-processing to eliminate various noises from EEG signals. There are many techniques used for pre-processing. For instance, the ResNet-50 model [99] was adapted to automatically extract EEG features and reduce the manual steps required for pre-processing data.
Categorizing EEG waveform is typically according to five frequency bands namely, Delta  ( δ ) , Theta  ( θ ) , Alpha  ( α ) , Beta  ( β ) , and Gamma  ( γ ) [34,74,79,95,100,101,102,103,104,105]. These bands include informative detail frequency for signal classification based on the waveform, such as sleep stage disorder classification [28,31]. Table 3 shows the various frequency and amplitude as recommended by the American Academy of Sleep Medicine (AASM).

2.5. Feature Extraction

After filtering and signal pre-processing, informative features needed to be extracted [43,80,106,107]. This was one of the critical steps for the application of ML models for bio-electric signals, and the appropriate design of this step has improved model performance [108,109]. Different ML models have been used for PSG data analysis [28,31]. Most used for PSG datasets required robust feature extraction that was sufficiently correlated. These features have been extracted based on uni-variate (measures taken on each channel separately), multi-variate (measures taken on two or more channels) [110], and multi-modal (measures taken from multiple modalities, such as EEG, ECG, EMG, and EOG) approaches.There are four predominant features commonly extracted from PSG data: (1) time-domain, (2) frequency-domain scale, (3) time–frequency domain, and (4) non-linear [39,111,112,113]. EEG has typically been analyzed for the frequency domain, while EOG and EMG have been analyzed for the time domain [36]. Power spectrum density (PSD) has been a common approach for feature extraction from EEG signals [114,115,116,117]. The most popular method of estimating PSD was based on the measure of the signal’s power from the device against the device’s time–frequency [34,47,71,118]. PSD was calculated using Welch and Fourier transformations [114,119,120,121,122,123]. Other widely researched feature extraction methods for PSG signals have included continuous wavelet transform (CWT) coefficients, autoregressive (AR) coefficients [124,125], and Hjorth parameters [126]. Zhang et al. [112,127] and Galvao et al. [87] discussed additional feature extraction methods. Table 4 shows a summary of feature extraction methods for PSG data.

2.6. Balancing Datasets

It has been established that PSG data in their raw state are not balanced, as a normal sleep pattern contains more non-REM sleep than REM sleep, as well as more light sleep than deep sleep [137]. The imbalance makes it difficult for an ML model to be trained effectively. Zhou et al. [138] studied different dataset-balancing approaches. Efe et al. [139] proposed a hybrid neural network architecture using focal-loss and discrete-cosine-transform methods to solve the training data imbalance. Utomo et al. [133] proposed a model based on ECG signal to address imbalanced learning challenges. Over-sampling and under-sampling have been two common strategies, but each has critical weaknesses. For instance, the straightforward and simple way to handle class imbalance has been to increase the minority class, i.e., over-sampling, but this approach disrupts the data architecture [140].

2.7. Machine-Learning Modeling

ML leverages the framework of mathematical modeling to classify, predict trends, and detect anomalies in specified time series [4,30,141,142]. In healthcare, ML has been used for the feature extraction and classification of disease in many studies [57,143,144]. There have been a plethora of ML approaches used for PSG data classification and performance improvement. The growth of research concerning AI and ML approaches as well as for the analysis of PSG datasets has shown an upward trend [145,146]. When applying ML techniques to any dataset, statistical and machine-learning models have been the two most common models applied [66,147], and this has been further broken down into sub-categories, including supervised, semi-supervised, and unsupervised learning [8,59,148,149]. PSG signals have been treated as multi-variate, multi-modal time series [150]. Lu et al. [7,40] concluded that deep learning was the most-used ML approach for feature extraction. A significant amount of research and other literature has explored both statistical and deep-learning approaches on PSG datasets [151], in which support vector machine was also widely studied in shallow ML approaches and CNNs for deep learning. Sarkar et al. [152] studied the suitability of recurrent neural networks (RNN) with long short-term memory (LSTM), support-vector-machine (SVM) [151,153,154], and logistic-regression (LR) models [155,156] to monitor depressive symptoms via EGGand found that under supervised learning, SVM and LR outperformed the others. In recent years, different ML models [40,46] have been used to classify and diagnose mental health, imagery, emotions, behaviors, etc. With the recent increase in the use of ML in the healthcare domain, some of these models have been intensely studied, while others have not been sufficiently explored. Thamaraimanalan et al. [157] proposed a radial basis function network (RBFN), which is a variation of artificial neural network (ANN) models. The main aim of the RBFN model was to solve problems faster and more accurately. The authors of [158] studied explainable artificial intelligence (XAI), which assisted the final users in obtaining a reasonable explanation as to underlying fundamentals of the AI model.There have been a plethora of models proposed in various studies. Below are some of the popular models noted in the literature selected for this review.
K-Nearest Neighbor (KNN): KNN has been shown to provide high accuracy for EEG-based emotion classifications [44,86,159,160]. It is a supervised learning method that was first developed in 1951. KNN has commonly been used for both classification and regression [161]. KNN is considered to be one of the simplest ML models. It promotes the concept of the “majority carries the day”. An object is classified based on the plurality vote of its neighbors [44]. There is a decrease in the classification speed as the number of variables increases. KNN algorithms are peculiar because of their sensitivity to the actual data structure.
Support Vector Machine (SVM): SVM is a kernel-based learning method, a supervised ML algorithm, which has also been commonly adopted for regression problems [154,159,162]. It has been widely studied and used for the classification of PSG datasets [161,163,164,165]. In many studies, SVM has resulted in a higher accuracy score than its unsupervised counterparts [161]. Similar to KNN, it is efficient in analyzing data for classification and regression. In contrast to KNN, however, SVM is a fast and reliable algorithm, and it also performs well with a limited amount of samples for analysis.
Logistic Regression (LR): LR uses a logistic function on the dependent variable [166]. Subani et al. [165] used LR to model the relationship between a reduced set of features and the corresponding treatment outcomes based on captured datasets that had been processed and feature-extracted [163,164,165]. For feature interpretation, LR model coefficients have been noted as indicators. Unknown records are easily classified, and it is easy to implement and interpret. When the datasets were linearly structured, LR was very effective [166], because LR assumes linearity among independent variables [166].
Extreme Learning Machine (ELM): ELM uses a single layer of feedforward neuron networks (SLFN) and chooses the input weights randomly [43,125,133,134,167,168]. ELM is a simplified form of an artificial neural network (ANN). ELM was invented in 2006. It differs from the other neural network model as it does not need gradient-based backpropagation to be trained. It is not as accurate as other neural network models. Kadam et al. [125] studied a different type of ELM, called hierarchical ELM, which extended the basic ELM to multiple layers. Hierarchical ELM was implemented as a supervised learning method.
Multi-Layer Perceptron (MLP): MLP is classified as a feedforward ANN [152,169,170] that has input, output, and hidden layers in its architecture [137]. It is credited as the algorithm that forms the base of a complex neural network. MLP classifies data that are not linearly separable. For difficult or complex datasets, MLP can be customized with a robust architecture to solve regression and classification tasks. In many applications, MLP has been shown to be sensitive to feature-scaling due to the option of its activation functions.
Long Short-Term Memory (LSTM): LSTM has been considered by many researchers as an effective and scalable model for several learning problems related to time-series data [7,8,13,35,82,105,119,169,171,172,173,174]. Using LSTM on PSG data has also resulted in much success. LSTM has been firmly established as a state-of-the-art approach in sequence modeling [175,176]. In addition, LSTM has been credited with advanced results in sequence-processing tasks [131,142,177,178,179,180,181,182,183]. The study in [175] presented a more robust model called a transformer, which was the first sequence-transduction model entirely based on attention and replaced recurrent layers [175,176,184].To the best of our knowledge, there have been few studies that have applied this model on a PSG dataset [185].
Convolutional Neural Network (CNN): A CNN is typically composed of two types of layers, where the convolutional layer is followed by a max-pooling layer [169,186,187,188]. CNNs are more commonly used for image recognition and feature extraction. Using a CNN alone has produced relatively low forecasting accuracy for time-series data; therefore, a CNN–LSTM hybrid model has been widely studied on PSG datasets [7,66,142,169,189,190,191,192,193,194,195,196]. For EEG-based analysis, it provided high accuracy and contained a non-linear domain due to its random and chaotic properties [192,194].
Spiking Neural Network (SNN): SNN is often referred to as the third generation of ANN [197]. It is a relatively rare approach used to model spatio-temporal brain data (STBD), and EEG is a well-known non-invasive type of STBD [198]. It has the ability to learn from changes in temporal data. SNN was inspired by information processing in biology [199]. Despite the increase in the research using SNN, SNN performance has been reported as relatively low, as compared to other ML counterparts [199]. This limitation was found in major benchmark datasets. However, because of SNN’s ability to measure biological spikes without further transformation issues, it has attracted the interest of AI researchers. The training time of SNN has been an impediment, due to the fact that SNN uses a more complex method, as compared to other CNN approaches [199].
Table 5 provides a summary of the studies using machine learning for the classification and prediction of PSG data.

2.8. Performance Evaluation

In this section, we discuss model performance measures, which quantified the effectiveness of a model for classifying or predicting new cases or disease conditions after being trained, validated, and tested using the available dataset. The results are described based on different aspects of performance [193,195,203,204]. Most of the papers in this review measured accuracy, precision, sensitivity (recall), specificity, F1-scores, and confusion matrices [13,54,97,205,206,207,208,209,210].
  • Sensitivity: It is also known as recall. This measures the ratio of the number of samples correctly predicted to the total samples in the class. Sensitivity can be calculated based on true positive (TP) and false negative (FN) parameters [31,208,211]. Equation (1) shows a mathematical representation of the sensitivity computation.
    Sensitivity ( S x ) = True Positive True Positive + False Negative
  • Accuracy: This is the fraction of samples that were correctly classified. Accuracy can be expressed as the ratio of the summation of true-positive (TP) and true-negative (TN) parameters to the total sample size, which includes true positive (TP), false positive (FP), false negative (FN), and true negative (TN) [31,137,208,211]. Equation (2) shows a mathematical representation of accuracy.
    Accuracy ( A c c ) = True Positive + True Negative True Positive + False Positive + True Negative + False Negative
  • Precision: It is the ratio of the samples correctly predicted to the total predicted positive samples. Equation (3) shows a mathematical representation of the precision computation.
    Precision ( P s ) = True Positive True Positive + False Positive
  • Specificity: It measures how many healthy (negative) samples were identified as healthy (negative) samples by a model. Equation (4) shows a mathematical representation of the specificity computation.
    Specificity ( S e ) = True Negative True Negative + False Positive
  • F1-score: It is a function of precision and sensitivity (recall). It is represented as the harmonic mean of sensitivity and precision. Equation (5) shows a mathematical representation of F1-score computation. F1-scores range from 0 to 1, with 1 being a perfect precision sensitivity (recall) and 0 being the lowest precision sensitivity. Equation (5) shows a mathematical representation of the F1-score computation.
    F 1 - score ( F 1 ) = 2 P s S x ( P s + S x )
The above are the most commonly used performance evaluation metrics for classification problems. Using accuracy alone to determine the performance of a classification model could be misleading. Calculating a confusion matrix provides a more accurate benchmark for evaluating the performance of classification models, particularly regarding their accuracy and suitability [54,107,204,212,213,214].

3. Summary and Discussion

The study of ML methodologies for measuring biomedical signals has, in recent years, attracted increased attention. In this work, the reviewed literature provided an overview of the application of ML approaches on PSG datasets.In this section, we summarize the advantages, the limitations, and the current research gaps concerning these models. We provide detailed steps for applying ML methods to multi-channel and multi-modal PSG data. Using ML methods for feature extraction, prediction, diagnosis, and disease classification has reduced the dependence of clinical professionals on the manual processing of PSG datasets.
ML facilitates a more robust and deeper understanding of PSG dataset processing. The benefits of ML for mental health diagnosis and classification have been confirmed.However, we reviewed the literature to identify the key steps for applying ML to PSG datasets, as well as the limitations and benefits.We discuss data-capturing, the types of datasets, data-processing, feature extraction, model classification, and performance evaluation.

3.1. Challenges of Using ML on Multi-Channel and Multi-Modal PSG Datasets

Data-capturing: Biomedical signals are often recorded using multiple electrodes. This leads to an increase in the dimension of recorded signals, which makes the analysis of multi-channel PSG datasets challenging. Typically, these multi-channel EEG signals are converted to single-channel signals for ease of analysis.
Recently, an increase in available PSG datasets have made ML research possible. Research conducted by Guillot et al. utilized eight different datasets [185]. In most of the articles reviewed in this work, many open-access datasets were used. The correct type of data increased the accuracy of the results. The limitations of certain datasets concern the issues of imbalance and noise. For satisfactory ML development, datasets must be cleaned to remove noise, as well as prepared, before applying a classification model.
Data-formatting: Biomedical signals are stored using different data formats, such as the European data format (EDF), the general data format (GDF), and BrainVision (VHDR, VMRK, EEG). It is standard practice to store PSG data in an EDF or EDF+ format, as these are simple and flexible formats for the exchange and storage of multi-channel biological, multi-modal, and physical signals [215,216]. However, the inconsistencies in data-formatting create barriers for the widespread use of a dataset in the ML research community.For example, in contrast to comma-separated-values (CSV) files that are commonly used for data storage, EDF and EDF+ are not as accommodating as CSV files and require a special tool to read and pre-process.
Data imbalance: PSG datasets must be processed and balanced for satisfactory classification performance. Due to the nature of these datasets, balancing all the channels in a multi-channel dataset is always a challenge. In many cases, there is a dominant class. We found a significant amount of literature that detailed the process of balancing a PSG dataset. Furthermore, there are issues with multi-modal datasets that have been included in PSG datasets, as these then have to be treated as a different modality. This also increases the complexity of balancing a PSG dataset.
Extracting features: In this study, we showed the most commonly used methods for feature extraction. However, different feature extraction methods can work according to different data properties. Extensive tests are usually required. PSG datasets often contain a significant amount of noise, making feature extraction difficult.
Classification model: Such as found in prediction models, there are training, validation, and testing datasets. Dividing PSG datasets into training, validation, and testing data poses a challenge because of insufficient labeling, large dataset sizes, and large time stamps. The presence of additional modalities in PSG datasets also poses a challenge for effective data fusion.
Performance evaluation: We found in this work that the most used performance evaluations for ML applications were sensitivity (recall), specificity, F1-score, and accuracy. Most of the literature in this review had calculated the model accuracy as a way of determining model performance, but only calculating accuracy was not an effective evaluation of the robustness of a model. It remained challenging to interpret information presented in PSG datasets without the assistance of experts to determine the actual performance of a classification model.In practice, sex and race were considered protected attributes. This increased concerns regarding the security of subjects’ or patients’ private information since the actual patient’s personal information was required for data-capturing. The measure of fairness for PSG datasets has also been challenging [217]. Fairness measures used for ML have been reported as not universally suitable [217].

3.2. Research Gaps

It was clear that ML offered significant benefits for diagnosis and classification of mental health issues when used correctly. We showed that when implementing ML for multi-variate multi-modal PSG datasets, a solid understanding of the steps and techniques was required.There are many techniques and methods that are highly dependent on the type of dataset. One major gap in the research was that the gold standard methods and techniques have yet to be clearly defined.
Data-capturing: As compared to other data-capturing procedure for ML application, sleep studies required an overnight period for data-capturing. Many patients reported this as "too long". In all the articles reviewed in this work, there was little effort to reduce this time. Furthermore, to the best of our knowledge, there has been limited research conducted concerning the reduction in the number of electrodes or sensors used to capture these datasets. Using a high number electrodes has been reported as uncomfortable by some patients [218,219].
Data-formatting: Increasing the accessibility of bio-electric datasets has been limited by using only EDF and EDF+ file extensions.Among the 204 articles selected for this review, none either proposed or developed a more widely accessible format.
Feature extraction: Establishing gold-standard feature-extraction techniques could improve their scalability and ease of use.
Classification modeling: Many existing studies have been based on typical ML models. There have been some proven classification models with robust performance on PSG datasets. SVM appeared to be a common model that many have used effectively on PSG datasets. There were many studies that used deep-learning methods. There were a few that used self-attention models on PSG datasets. More advanced models should be considered, such as transfer learning, explainable machine learning, and robust learning.

4. Conclusions and Future Work

This study reviewed over 200 articles and their contributions towards the application of ML techniques for the diagnosis of mental health issues. According to the literature related to sleep studies and other mental health disorders, ML approaches have improved diagnostic accuracy, as compared to traditional manual processes, and this trend is likely to continue.More and more researchers are leveraging ML and AI tools to improve various aspects of the healthcare environment. There is still more research needed to advance the reliability and efficiency of these techniques. In this study, we focused on providing the detailed steps involved when applying ML to PSG datasets.
Based on the literature reviewed in this work and on the basis of our own knowledge, more research should be conducted regarding the application of attention-based models. We plan on creating a benchmark for the implementation of ML techniques on PSG datasets. Currently, there have been various techniques proposed, with most indicating robust performance enhancements. We plan on researching methods to assist researchers in the selection of the best classification models and feature extraction techniques.

Author Contributions

Conceptualization, J.E. and H.W.; Methodology, J.E.; Software, J.E.; Validation, J.E.; Investigation, J.E.; Data curation, J.E.; Writing—original draft, J.E.; Writing—review & editing, J.E. and H.W.; Visualization, J.E.; Supervision, H.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Nomenclatures

The following terms were used in this manuscript:
AASMAmerican Academy of Sleep Medicine
ADHDAttention-Deficit Hyperactivity Disorder
AIArtificial Intelligence
ANNArtificial Neural Network
CNNConvolutional Neural Networks
ECGElectrocardiograph
EEGElectroencephalogram
ELMExtreme Learning Machine
EMGElectromyogram
EOGElectro-oculogram
FFTFast Fourier Transformation
HRVHeart Rate Variability
LRLogistic Regression
LSTMLong-Short Term Memory
MLMachine Learning
NREMNon-Rapid Eye Movement
REMRapid Eye Movement
RFRandom Forest
RNNRecurrent Neural Networks
RKRechtschaffen and Kales
PCAPrincipal Component Analysis
PRISMAPreferred Reporting Items for Systematic Reviews and Meta-Analyses
PSDPower Spectral Density
SNNSpike Neural Network
PSGPolysomnography
SPO2Saturation of Peripheral Oxygen
SVMSupport Vector Machine

References

  1. Goetz, C.; Bavaresco, R.; Kunst, R.; Barbosa, J. Industrial intelligence in the care of workers’ mental health: A review of status and challenges. Int. J. Ind. Ergon. 2022, 87, 103234. [Google Scholar] [CrossRef]
  2. Ramos-Lima, L.F.; Waikamp, V.; Antonelli-Salgado, T.; Passos, I.C.; Freitas, L.H.M. The use of machine learning techniques in trauma-related disorders: A systematic review. J. Psychiatr. Res. 2020, 121, 159–172. [Google Scholar] [CrossRef] [PubMed]
  3. Li, Y.; Li, N.; Zhang, L.; Liu, Y.; Zhang, T.; Li, D.; Bai, D.; Liu, X.; Li, L. Predicting PTSD symptoms in firefighters using a fear-potentiated startle paradigm and machine learning. J. Affect. Disord. 2022, 319, 294–299. [Google Scholar] [CrossRef] [PubMed]
  4. Sumathi, M.S.; Joshi, C.S.; Thomas, R.R.; Reethu, G. Analysis and Performance of Machine Learning Algorithms on Disease Diagnosis. In Proceedings of the 2020 3rd International Conference on Energy, Power and Environment: Towards Clean Energy Technologies, Shanghai, China, 12–13 July 2021; IEEE: Shillong, India, 2021; pp. 1–6. [Google Scholar] [CrossRef]
  5. Rejaibi, E. MFCC-based Recurrent Neural Network for automatic clinical depression recognition and assessment from speech. Biomed. Signal Process. Control. 2022, 11. [Google Scholar] [CrossRef]
  6. Gore, E.; Rathi, S. Types of Data with Algorithms for Assessing Mental Health Conditions. In Proceedings of the 2019 5th International Conference on Computing, Communication, Control and Automation (ICCUBEA), Pune, India, 19–21 September 2019; IEEE: Pune, India, 2019; pp. 1–8. [Google Scholar] [CrossRef]
  7. Lu, W.; Li, J.; Li, Y.; Sun, A.; Wang, J. A CNN-LSTM-Based Model to Forecast Stock Prices. Complexity 2020, 2020, 6622927. [Google Scholar] [CrossRef]
  8. Zhang, C.; Song, D.; Chen, Y.; Feng, X.; Lumezanu, C.; Cheng, W.; Ni, J.; Zong, B.; Chen, H.; Chawla, N.V. A Deep Neural Network for Unsupervised Anomaly Detection and Diagnosis in Multivariate Time Series Data. Proc. AAAI Conf. Artif. Intell. 2019, 33, 1409–1416. [Google Scholar] [CrossRef] [Green Version]
  9. Li, J.; Izakian, H.; Pedrycz, W.; Jamal, I. Clustering-based anomaly detection in multi-variate time-series data. Appl. Soft Comput. 2021, 100, 106919. [Google Scholar] [CrossRef]
  10. Manjunath, S.; Nathaniel, A.; Druce, J.; German, S. Improving the Performance of Fine-Grain Image Classifiers via Generative Data Augmentation. arXiv 2020. [Google Scholar] [CrossRef]
  11. Goldstein, M.; Uchida, S. A Comparative Evaluation of Unsupervised Anomaly Detection Algorithms for Multivariate Data. PLoS ONE 2016, 11, e0152173. [Google Scholar] [CrossRef] [Green Version]
  12. Sabry, F.; Eltaras, T.; Labda, W.; Alzoubi, K.; Malluhi, Q. Machine Learning for Healthcare Wearable Devices: The Big Picture. J. Healthc. Eng. 2022, 2022, 4653923. [Google Scholar] [CrossRef]
  13. Mehdiyev, N.; Lahann, J.; Emrich, A.; Enke, D.; Fettke, P.; Loos, P. Time Series Classification using Deep Learning for Process Planning: A Case from the Process Industry. Procedia Comput. Sci. 2017, 114, 242–249. [Google Scholar] [CrossRef]
  14. Li, J. Multi-modal bio-electrical signal fusion analysis based on different acquisition devices and scene settings: Overview, challenges, and novel orientation. Inf. Fusion 2022, 79, 229–247. [Google Scholar] [CrossRef]
  15. Saeidi, M.; Karwowski, W.; Farahani, F.V.; Fiok, K.; Taiar, R.; Hancock, P.A.; Al-Juaid, A. Neural Decoding of EEG Signals with Machine Learning: A Systematic Review. Brain Sci. 2021, 11, 1525. [Google Scholar] [CrossRef] [PubMed]
  16. Heo, J.; Yoon, H.; Park, K. A Novel Wearable Forehead EOG Measurement System for Human Computer Interfaces. Sensors 2017, 17, 1485. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Hallett, M.; DelRosso, L.M.; Elble, R.; Ferri, R.; Horak, F.B.; Lehericy, S.; Mancini, M.; Matsuhashi, M.; Matsumoto, R.; Muthuraman, M.; et al. Evaluation of movement and brain activity. Clin. Neurophysiol. 2021, 132, 2608–2638. [Google Scholar] [CrossRef] [PubMed]
  18. Wang, F.; Wei, X.; Guo, J.; Zheng, Y.; Li, J.; Du, S. Research Progress of Rehabilitation Exoskeletal Robot and Evaluation Methodologies Based on Bio-electrical Signals. In Proceedings of the 2019 IEEE 9th Annual International Conference on CYBER Technology in Automation, Control, and Intelligent Systems (CYBER), Suzhou, China, 29 July–2 August 2019; IEEE: Suzhou, China, 2019; pp. 826–831. [Google Scholar] [CrossRef]
  19. Bleakley, L.E.; Keenan, R.J.; Graven, R.D.; Metha, J.A.; Ma, S.; Daykin, H.; Cornthwaite-Duncan, L.; Hoyer, D.; Reid, C.A.; Jacobson, L.H. Altered EEG power spectrum, but not sleep-wake architecture, in HCN1 knockout mice. Behav. Brain Res. 2023, 437, 114105. [Google Scholar] [CrossRef] [PubMed]
  20. Bi, X.; Wang, H. Early Alzheimer’s disease diagnosis based on EEG spectral images using deep learning. Neural Netw. 2019, 114, 119–135. [Google Scholar] [CrossRef]
  21. Martinek, R.; Ladrova, M.; Sidikova, M.; Jaros, R.; Behbehani, K.; Kahankova, R.; Kawala-Sterniuk, A. Advanced Bio-electrical Signal Processing Methods: Past, Present and Future Approach—Part II: Brain Signals. Sensors 2021, 21, 6343. [Google Scholar] [CrossRef]
  22. Kaplan, K.A.; Hardas, P.P.; Redline, S.; Zeitzer, J.M. Correlates of sleep quality in midlife and beyond: A machine learning analysis. Sleep Med. 2017, 34, 162–167. [Google Scholar] [CrossRef]
  23. Gerla, V.; Kremen, V.; Macas, M.; Dudysova, D.; Mladek, A.; Sos, P.; Lhotska, L. Iterative expert-in-the-loop classification of sleep PSG recordings using a hierarchical clustering. J. Neurosci. Methods 2019, 317, 61–70. [Google Scholar] [CrossRef]
  24. Biswal, S.; Sun, H.; Goparaju, B.; Westover, M.B.; Sun, J.; Bianchi, M.T. Expert-level sleep scoring with deep neural networks. J. Am. Med. Inform. Assoc. 2018, 25, 1643–1650. [Google Scholar] [CrossRef] [Green Version]
  25. Chambon, S.; Galtier, M.N.; Arnal, P.J.; Wainrib, G.; Gramfort, A. A Deep Learning Architecture for Temporal Sleep Stage Classification Using Multivariate and Multimodal Time Series. IEEE Trans. Neural Syst. Rehabil. Eng. 2018, 26, 758–769. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Sharma, M.; Patel, V.; Acharya, U.R. Automated identification of insomnia using optimal bi-orthogonal wavelet transform technique with single-channel EEG signals. Knowl.-Based Syst. 2021, 224, 107078. [Google Scholar] [CrossRef]
  27. Zaffaroni, A.; Coffey, S.; Dodd, S.; Kilroy, H.; Lyon, G.; O’Rourke, D.; Lederer, K.; Fietze, I.; Penzel, T. Sleep Staging Monitoring Based on Sonar Smartphone Technology. In Proceedings of the 2019 41st Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), Berlin, Germany, 23–27 July 2019; IEEE: Berlin, Germany, 2019; pp. 2230–2233. [Google Scholar] [CrossRef]
  28. Ravan, M. A machine learning approach using EEG signals to measure sleep quality. AIMS Electron. Electr. Eng. 2019, 3, 347–358. [Google Scholar] [CrossRef]
  29. Wang, H.; Lu, C.; Zhang, Q.; Hu, Z.; Yuan, X.; Zhang, P.; Liu, W. A novel sleep staging network based on multi-scale dual attention. Biomed. Signal Process. Control 2022, 74, 103486. [Google Scholar] [CrossRef]
  30. Ramachandran, A.; Karuppiah, A. A Survey on Recent Advances in Machine Learning Based Sleep Apnea Detection Systems. Healthcare 2021, 9, 914. [Google Scholar] [CrossRef] [PubMed]
  31. Aboalayon, K.; Faezipour, M.; Almuhammadi, W.; Moslehpour, S. Sleep Stage Classification Using EEG Signal Analysis: A Comprehensive Survey and New Investigation. Entropy 2016, 18, 272. [Google Scholar] [CrossRef]
  32. Xu, S.; Faust, O.; Seoni, S.; Chakraborty, S.; Barua, P.D.; Loh, H.W.; Elphick, H.; Molinari, F.; Acharya, U.R. A review of automated sleep disorder detection. Comput. Biol. Med. 2022, 150, 106100. [Google Scholar] [CrossRef]
  33. Acharya, U.R.; Oh, S.L.; Hagiwara, Y.; Tan, J.H.; Adeli, H.; Subha, D.P. Automated EEG-based screening of depression using deep convolutional neural network. Comput. Methods Programs Biomed. 2018, 161, 103–113. [Google Scholar] [CrossRef]
  34. Liu, S.; Shen, J.; Li, Y.; Wang, J.; Wang, J.; Xu, J.; Wang, Q.; Chen, R. EEG Power Spectral Analysis of Abnormal Cortical Activations During REM/NREM Sleep in Obstructive Sleep Apnea. Front. Neurol. 2021, 12, 643855. [Google Scholar] [CrossRef]
  35. Ay, B.; Yildirim, O.; Talo, M.; Baloglu, U.B.; Aydin, G.; Puthankattil, S.D.; Acharya, U.R. Automated Depression Detection Using Deep Representation and Sequence Learning with EEG Signals. J. Med. Syst. 2019, 43, 205. [Google Scholar] [CrossRef]
  36. Zoubek, L.; Charbonnier, S.; Lesecq, S.; Buguet, A.; Chapotot, F. Feature selection for sleep/wake stages classification using data driven methods. Biomed. Signal Process. Control 2007, 2, 171–179. [Google Scholar] [CrossRef]
  37. Rezaei, M.; Mohammadi, H.; Khazaie, H. EEG/EOG/EMG data from a cross sectional study on psychophysiological insomnia and normal sleep subjects. Data Brief 2017, 15, 314–319. [Google Scholar] [CrossRef] [PubMed]
  38. Satapathy, S.K.; Bhoi, A.K.; Loganathan, D.; Khandelwal, B.; Barsocchi, P. Machine learning with ensemble stacking model for automated sleep staging using dual-channel EEG signal. Biomed. Signal Process. Control 2021, 69, 102898. [Google Scholar] [CrossRef]
  39. Gao, W.; Xu, Y.; Li, S.; Fu, Y.; Zheng, D.; She, Y. Obstructive sleep apnea syndrome detection based on ballistocardiogram via machine learning approach. Math. Biosci. Eng. 2019, 16, 5672–5686. [Google Scholar] [CrossRef]
  40. Salama, E.S. A 3D-convolutional neural network framework with ensemble learning techniques for multi-modal emotion recognition. Egypt. Inform. J. 2021, 22, 167–176. [Google Scholar] [CrossRef]
  41. Langer, N.; Plomecka, M.B.; Tröndle, M.; Negi, A.; Popov, T.; Milham, M.; Haufe, S. A benchmark for prediction of psychiatric multimorbidity from resting EEG data in a large pediatric sample. NeuroImage 2022, 258, 119348. [Google Scholar] [CrossRef]
  42. Uwaechia, A.N.; Ramli, D.A. A Comprehensive Survey on ECG Signals as New Biometric Modality for Human Authentication: Recent Advances and Future Challenges. IEEE Access 2021, 9, 97760–97802. [Google Scholar] [CrossRef]
  43. Rakshith, V.; Apoorv, V.; Akarsh, N.K.; Arjun, K.; Krupa, B.N.; Pratima, M.; Vedamurthachar, A. A novel approach for the identification of chronic alcohol users from ECG signals. In Proceedings of the TENCON 201–2017 IEEE Region 10 Conference, Penang, Malaysia, 5–8 November 2017; IEEE: Penang, Malaysia, 2017; pp. 1321–1326. [Google Scholar] [CrossRef]
  44. Vuksanovic, B. Analysis of Human Electrocardiogram for Biometric Recognition Using Analytic and AR Modeling Extracted Parameters. Int. J. Inf. Electron. Eng. 2014, 4. [Google Scholar] [CrossRef]
  45. Said, S.; Nait-ali, A. Machine-Learning based Wearable Multi-Channel sEMG Biometrics Modality for User’s Identification. In Proceedings of the 2021 4th International Conference on Bio-Engineering for Smart Technologies (BioSMART), Paris/Créteil, France, 8–10 December 2021; p. 4. [Google Scholar]
  46. Pigoni, A.; Delvecchio, G.; Madonna, D.; Bressi, C.; Soares, J.; Brambilla, P. Can Machine Learning help us in dealing with treatment resistant depression? A review. J. Affect. Disord. 2019, 259, 21–26. [Google Scholar] [CrossRef]
  47. Combrisson, E.; Vallat, R.; Eichenlaub, J.B.; O’Reilly, C.; Lajnef, T.; Guillot, A.; Ruby, P.M.; Jerbi, K. Sleep: An Open-Source Python Software for Visualization, Analysis, and Staging of Sleep Data. Front. Neuroinform. 2017, 11, 60. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Supratak, A.; Dong, H.; Wu, C.; Guo, Y. DeepSleepNet: A Model for Automatic Sleep Stage Scoring Based on Raw Single-Channel EEG. IEEE Trans. Neural Syst. Rehabil. Eng. 2017, 25, 1998–2008. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Moser, D.; Anderer, P.; Gruber, G.; Parapatics, S.; Loretz, E.; Boeck, M.; Kloesch, G.; Heller, E.; Schmidt, A.; Danker-Hopfe, H.; et al. Sleep Classification According to AASM and Rechtschaffen & Kales: Effects on Sleep Scoring Parameters. Sleep 2009, 32, 139–149. [Google Scholar]
  50. The AASM-Manual for Scoring Sleep and Associated Event. Available online: https://aasm.org/clinical-resources/scoring-manual/ (accessed on 21 February 2023).
  51. Huang, C.S.; Lin, C.L.; Ko, L.W.; Liu, S.Y.; Sua, T.P.; Lin, C.T. A hierarchical classification system for sleep stage scoring via forehead EEG signals. In Proceedings of the 2013 IEEE Symposium on Computational Intelligence, Cognitive Algorithms, Mind, and Brain (CCMB), Singapore, 16–19 April 2013; IEEE: Singapore, 2013; pp. 1–5. [Google Scholar] [CrossRef]
  52. Ghaderyan, P.; Moghaddam, F.; Khoshnoud, S.; Shamsi, M. New interdependence feature of EEG signals as a biomarker of timing deficits evaluated in Attention-Deficit/Hyperactivity Disorder detection. Measurement 2022, 199, 111468. [Google Scholar] [CrossRef]
  53. Lee, W.; Kim, G.; Yu, J.; Kim, Y. Model Interpretation Considering Both Time and Frequency Axes Given Time Series Data. Appl. Sci. 2022, 12, 12807. [Google Scholar] [CrossRef]
  54. Dev, A.; Roy, N.; Islam, M.K.; Biswas, C.; Ahmed, H.U.; Amin, M.A.; Sarker, F.; Vaidyanathan, R.; Mamun, K.A. Exploration of EEG-Based Depression Biomarkers Identification Techniques and Their Applications: A Systematic Review. IEEE Access 2022, 10, 16756–16781. [Google Scholar] [CrossRef]
  55. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef]
  56. Sharma, L.D.; Bohat, V.K.; Habib, M.; Al-Zoubi, A.M.; Faris, H.; Aljarah, I. Evolutionary inspired approach for mental stress detection using EEG signal. Expert Syst. Appl. 2022, 197, 116634. [Google Scholar] [CrossRef]
  57. Motwani, A.; Shukla, P.K.; Pawar, M. Ubiquitous and smart healthcare monitoring frameworks based on machine learning: A comprehensive review. Artif. Intell. Med. 2022, 134, 102431. [Google Scholar] [CrossRef]
  58. Barros, C.; Silva, C.A.; Pinheiro, A.P. Advanced EEG-based learning approaches to predict schizophrenia: Promises and pitfalls. Artif. Intell. Med. 2021, 114, 102039. [Google Scholar] [CrossRef]
  59. Mirchi, N.; Warsi, N.M.; Zhang, F.; Wong, S.M.; Suresh, H.; Mithani, K.; Erdman, L.; Ibrahim, G.M. Decoding Intracranial EEG With Machine Learning: A Systematic Review. Front. Hum. Neurosci. 2022, 16, 913777. [Google Scholar] [CrossRef] [PubMed]
  60. Thieme, A.; Belgrave, D.; Doherty, G. Machine Learning in Mental Health: A Systematic Review of the HCI Literature to Support the Development of Effective and Implementable ML Systems. ACM Trans. Comput.-Hum. Interact. 2020, 27, 1–53. [Google Scholar] [CrossRef]
  61. Boukobza, A.; Burgun, A.; Roudier, B.; Tsopra, R. Deep Neural Networks for Simultaneously Capturing Public Topics and Sentiments During a Pandemic: Application on a COVID-19 Tweet Data Set. JMIR Med. Inform. 2022, 10, e34306. [Google Scholar] [CrossRef] [PubMed]
  62. Gramfort, A.; Luessi, M.; Larson, E.; Engemann, D.A.; Strohmeier, D.; Brodbeck, C.; Goj, R.; Jas, M.; Brooks, T.; Parkkonen, L.; et al. MEG and EEG Data Analysis with MNE-Python. Front. Neurosci. 2013, 7, 1–13. [Google Scholar] [CrossRef] [Green Version]
  63. Sekkal, R.N.; Bereksi-Reguig, F.; Ruiz-Fernandez, D.; Dib, N.; Sekkal, S. Automatic sleep-stage classification: From classical machine learning methods to deep learning. Biomed. Signal Process. Control 2022, 77, 103751. [Google Scholar] [CrossRef]
  64. Pepi, C.; Mercier, M.; Carfì Pavia, G.; de Benedictis, A.; Vigevano, F.; Rossi-Espagnet, M.C.; Falcicchio, G.; Marras, C.E.; Specchio, N.; de Palma, L. Can Presurgical Interhemispheric EEG Connectivity Predict Outcome in Hemispheric Surgery? A Brain Machine Learning Approach. Brain Sci. 2023, 13, 71. [Google Scholar] [CrossRef]
  65. ElMoaqet, H.; Eid, M.; Ryalat, M.; Penzel, T. A Deep Transfer Learning Framework for Sleep Stage Classification with Single-Channel EEG Signals. Sensors 2022, 22, 8826. [Google Scholar] [CrossRef]
  66. Ehiabhi, J.; Wang, H. An Unsupervised Anomaly Detection Model for Multivariate Time Series Data. In Proceedings of the IISE ANNUAL Conference, Seattle, DC, USA, 21 May 2022; p. 7. [Google Scholar]
  67. Ameera, A.; Saidatul, A.; Ibrahim, Z. Analysis of EEG Spectrum Bands Using Power Spectral Density for Pleasure and Displeasure State. IOP Conf. Ser. Mater. Sci. Eng. 2019, 557, 012030. [Google Scholar] [CrossRef]
  68. Lee, H.; Li, B.; DeForte, S.; Splaingard, M.; Huang, Y.; Chi, Y.; Linwood, S.L. A Large Collection of Real-world Pediatric Sleep Studies. Sci. Data 2022, 9, 421. [Google Scholar] [CrossRef]
  69. O’Reilly, C.; Gosselin, N.; Carrier, J.; Nielsen, T. Montreal Archive of Sleep Studies: An open-access resource for instrument benchmarking and exploratory research. J. Sleep Res. 2014, 23, 628–635. [Google Scholar] [CrossRef]
  70. Goldberger, A.L.; Amaral, L.A.N.; Glass, L.; Hausdorff, J.M.; Ivanov, P.C.; Mark, R.G.; Mietus, J.E.; Moody, G.B.; Peng, C.K.; Stanley, H.E. PhysioBank, PhysioToolkit, and PhysioNet: Components of a New Research Resource for Complex Physiologic Signals. Circulation 2000, 101. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. Memis, G.; Sert, M. Multimodal Classification of Obstructive Sleep Apnea Using Feature Level Fusion. In Proceedings of the 2017 IEEE 11th International Conference on Semantic Computing (ICSC), San Diego, CA, USA, 30 January–1 February 2017; IEEE: San Diego, CA, USA, 2017; pp. 85–88. [Google Scholar] [CrossRef]
  72. Khosla, A.; Khandnor, P.; Chand, T. Automated diagnosis of depression from EEG signals using traditional and deep-learning approaches: A comparative analysis. Biocybern. Biomed. Eng. 2022, 42, 108–142. [Google Scholar] [CrossRef]
  73. Engemann, D.A.; Mellot, A.; Höchenberger, R.; Banville, H.; Sabbagh, D.; Gemein, L.; Ball, T.; Gramfort, A. A reusable benchmark of brain-age prediction from M/EEG resting-state signals. NeuroImage 2022, 262, 119521. [Google Scholar] [CrossRef] [PubMed]
  74. Khalighi, S.; Sousa, T.; Santos, J.M.; Nunes, U. ISRUC-Sleep: A comprehensive public dataset for sleep researchers. Comput. Methods Programs Biomed. 2016, 124, 180–192. [Google Scholar] [CrossRef] [PubMed]
  75. Ranjan, R.; Sahana, B.C. Automatic Detection of Mental Health Status using Alpha Subband of EEG Data. In Proceedings of the 2022 IEEE International Symposium on Medical Measurements and Applications (MeMeA), Messina, Italy, 2–24 June 2022; IEEE: Messina, Italy, 2022; pp. 1–6. [Google Scholar] [CrossRef]
  76. Jain, R.; Ganesan, R.A. Reliable sleep staging of unseen subjects with fusion of multiple EEG features and RUSBoost. Biomed. Signal Process. Control 2021, 70, 103061. [Google Scholar] [CrossRef]
  77. Supakar, R.; Satvaya, P.; Chakrabarti, P. A deep learning based model using RNN-LSTM for the Detection of Schizophrenia from EEG data. Comput. Biol. Med. 2022, 151, 106225. [Google Scholar] [CrossRef] [PubMed]
  78. Rasheed, K.; Qadir, J.; O’Brien, T.J.; Kuhlmann, L.; Razi, A. A Generative Model to Synthesize EEG Data for Epileptic Seizure Prediction. IEEE Trans. Neural Syst. Rehabil. Eng. 2021, 29, 2322–2332. [Google Scholar] [CrossRef]
  79. Chatterjee, R.; Maitra, T.; Hafizul Islam, S.; Hassan, M.M.; Alamri, A.; Fortino, G. A novel machine learning based feature selection for motor imagery EEG signal classification in Internet of medical things environment. Future Gener. Comput. Syst. 2019, 98, 419–434. [Google Scholar] [CrossRef]
  80. Alam, M.N.; Ibrahimy, M.I.; Motakabber, S.M.A. Feature Extraction of EEG Signal by Power Spectral Density for Motor Imagery Based BCI. In Proceedings of the 2021 8th International Conference on Computer and Communication Engineering (ICCCE), Kuala Lumpur, Malaysia, 9–10 April 2021; IEEE: Kuala Lumpur, Malaysia, 2021; pp. 234–237. [Google Scholar] [CrossRef]
  81. Tang, M.; Zhang, Z.; He, Z.; Li, W.; Mou, X.; Du, L.; Wang, P.; Zhao, Z.; Chen, X.; Li, X.; et al. Deep adaptation network for subject-specific sleep stage classification based on a single-lead ECG. Biomed. Signal Process. Control 2022, 75, 103548. [Google Scholar] [CrossRef]
  82. Alvarez-Estevez, D.; Rijsman, R.M. Inter-database validation of a deep-learning approach for automatic sleep scoring. PLoS ONE 2021, 16, e0256111. [Google Scholar] [CrossRef]
  83. Palotti, J.; Mall, R.; Aupetit, M.; Rueschman, M.; Singh, M.; Sathyanarayana, A.; Taheri, S.; Fernandez-Luque, L. Benchmark on a large cohort for sleep-wake classification with machine learning techniques. NPJ Digit. Med. 2019, 2, 50. [Google Scholar] [CrossRef] [Green Version]
  84. Zarei, A.; Beheshti, H.; Asl, B.M. Detection of sleep apnea using deep neural networks and single-lead ECG signals. Biomed. Signal Process. Control 2022, 71, 103125. [Google Scholar] [CrossRef]
  85. Zhao, R.; Xia, Y.; Wang, Q. Dual-modal and multi-scale deep neural networks for sleep staging using EEG and ECG signals. Biomed. Signal Process. Control 2021, 66, 102455. [Google Scholar] [CrossRef]
  86. Pisipati, M.; Nandy, A. Human Emotion Recognition using EEG Signal in Music Listening. In Proceedings of the 2021 IEEE 18th India Council International Conference (INDICON), Guwahati, India, 19–21 December 2021; IEEE: Guwahati, India, 2021; pp. 1–6. [Google Scholar] [CrossRef]
  87. Galvão, F.; Alarcão, S.M.; Fonseca, M.J. Predicting Exact Valence and Arousal Values from EEG. Sensors 2021, 21, 3414. [Google Scholar] [CrossRef]
  88. Qu, W.; Kao, C.H.; Hong, H.; Chi, Z.; Grunstein, R.; Gordon, C.; Wang, Z. Single-channel EEG based insomnia detection with domain adaptation. Comput. Biol. Med. 2021, 139, 104989. [Google Scholar] [CrossRef]
  89. Abdelhameed, A.M.; Bayoumi, M. Semi-Supervised EEG Signals Classification System for Epileptic Seizure Detection. IEEE Signal Process. Lett. 2019, 26, 1922–1926. [Google Scholar] [CrossRef]
  90. Pourmohammadi, S.; Maleki, A. Stress detection using ECG and EMG signals: A comprehensive study. Comput. Methods Programs Biomed. 2020, 193, 105482. [Google Scholar] [CrossRef] [PubMed]
  91. Zhu, S.; Qi, J.; Hu, J.; Hao, S. A new approach for product evaluation based on integration of EEG and eye-tracking. Adv. Eng. Inform. 2022, 52, 101601. [Google Scholar] [CrossRef]
  92. Sridhar, N.; Shoeb, A.; Stephens, P.; Kharbouch, A.; Shimol, D.B.; Burkart, J.; Ghoreyshi, A.; Myers, L. Deep learning for automated sleep staging using instantaneous heart rate. NPJ Digit. Med. 2020, 3, 106. [Google Scholar] [CrossRef] [PubMed]
  93. Petroff, O.A.; Spencer, D.D.; Goncharova, I.I.; Zaveri, H.P. A comparison of the power spectral density of scalp EEG and subjacent electrocorticograms. Clin. Neurophysiol. 2016, 127, 1108–1112. [Google Scholar] [CrossRef] [PubMed]
  94. Unde, S.A.; Shriram, R. Coherence Analysis of EEG Signal Using Power Spectral Density. In Proceedings of the 2014 Fourth International Conference on Communication Systems and Network Technologies, Bhopal, India, 7–9 April 2014; IEEE: Bhopal, India, 2014; pp. 871–874. [Google Scholar] [CrossRef]
  95. Nagar, P.; Sethia, D. Brain Mapping Based Stress Identification Using Portable EEG Based Device. In Proceedings of the 2019 11th International Conference on Communication Systems & Networks (COMSNETS), Bengaluru, India, 7–11 January 2019; IEEE: Bengaluru, India, 2019; pp. 601–606. [Google Scholar] [CrossRef]
  96. Weon, H.W.; Byun, Y.E.; Lim, H.J. Quantitative EEG (QEEG) Analysis of Emotional Interaction between Abusers and Victims in Intimate Partner Violence: A Pilot Study. Brain Sci. 2021, 11, 570. [Google Scholar] [CrossRef] [PubMed]
  97. El-Sappagh, S.; Alonso, J.M.; Islam, S.M.R.; Sultan, A.M.; Kwak, K.S. A multilayer multi-modal detection and prediction model based on explainable artificial intelligence for Alzheimer’s disease. Sci. Rep. 2021, 11, 2660. [Google Scholar] [CrossRef] [PubMed]
  98. Vidhya, R.B.; Jerritta, S. Pre-processing ECG signals for smart home material application. Mater. Today Proc. 2022, 49, 2955–2961. [Google Scholar] [CrossRef]
  99. Tian, T.; Wang, L.; Luo, M.; Sun, Y.; Liu, X. ResNet-50 based technique for EEG image characterization due to varying environmental stimuli. Comput. Methods Programs Biomed. 2022, 225, 107092. [Google Scholar] [CrossRef] [PubMed]
  100. Kora, P.; Meenakshi, K.; Swaraja, K.; Rajani, A.; Raju, M.S. EEG based interpretation of human brain activity during yoga and meditation using machine learning: A systematic review. Complement. Ther. Clin. Pract. 2021, 43, 101329. [Google Scholar] [CrossRef] [PubMed]
  101. Sharif, M.S.; Theeng Tamang, M.R.; Fu, C. Predicting the Health Impacts of Commuting Using EEG Signal Based on Intelligent Approach. In Proceedings of the 2021 International Conference on Innovation and Intelligence for Informatics, Computing, and Technologies (3ICT), Zallaq, Bahrain, 29–30 September 2021; IEEE: Zallaq, Bahrain, 2021; pp. 386–391. [Google Scholar] [CrossRef]
  102. Uchida, S.; Maloney, T.; Feinberg, I. Sigma (12–16 Hz) and beta (20–28 Hz) EEG discriminate NREM and REM sleep. Brain Res. 1994, 659, 243–248. [Google Scholar] [CrossRef] [PubMed]
  103. Quintero-Zea, A.; Lopez, J.D.; Smith, K.; Trujillo, N.; Parra, M.A.; Escudero, J. Phenotyping Ex-Combatants From EEG Scalp Connectivity. IEEE Access 2018, 6, 55090–55098. [Google Scholar] [CrossRef]
  104. Hsu, Y.L.; Yang, Y.T.; Wang, J.S.; Hsu, C.Y. Automatic sleep stage recurrent neural classifier using energy features of EEG signals. Neurocomputing 2013, 104, 105–114. [Google Scholar] [CrossRef]
  105. Patnaik, S.; Moharkar, L.; Chaudhari, A. Deep RNN learning for EEG based functional brain state inference. In Proceedings of the 2017 International Conference on Advances in Computing, Communication and Control (ICAC3), Mumbai, India, 1–2 December 2017; IEEE: Mumbai, India, 2017; pp. 1–6. [Google Scholar] [CrossRef]
  106. Kim, C.; Sun, J.; Liu, D.; Wang, Q.; Paek, S. An effective feature extraction method by power spectral density of EEG signal for 2-class motor imagery-based BCI. Med. Biol. Eng. Comput. 2018, 56, 1645–1658. [Google Scholar] [CrossRef]
  107. Zhou, J.; Wang, G.; Liu, J.; Wu, D.; Xu, W.; Wang, Z.; Ye, J.; Xia, M.; Hu, Y.; Tian, Y. Automatic Sleep Stage Classification With Single Channel EEG Signal Based on Two-Layer Stacked Ensemble Model. IEEE Access 2020, 8, 57283–57297. [Google Scholar] [CrossRef]
  108. Faisal, M.A.A.; Chowdhury, M.E.; Khandakar, A.; Hossain, M.S.; Alhatou, M.; Mahmud, S.; Ara, I.; Sheikh, S.I.; Ahmed, M.U. An investigation to study the effects of Tai Chi on human gait dynamics using classical machine learning. Comput. Biol. Med. 2022, 142, 105184. [Google Scholar] [CrossRef] [PubMed]
  109. Majhi, M.K.; Pradhan, B.K.; Sarkar, P.; Sivaraman, J.; Pal, K. Can statistical and entropy-based features extracted from ECG signals efficiently differentiate the cannabis-consuming women population from the non-consumer? Med. Hypotheses 2022, 167, 110952. [Google Scholar] [CrossRef]
  110. Rasheed, K.; Qayyum, A.; Qadir, J.; Sivathamboo, S.; Kwan, P.; Kuhlmann, L.; O’Brien, T.; Razi, A. Machine Learning for Predicting Epileptic Seizures Using EEG Signals: A Review. IEEE Rev. Biomed. Eng. 2021, 14, 139–155. [Google Scholar] [CrossRef] [PubMed]
  111. Cruz-Garza, J.G.; Darfler, M.; Rounds, J.D.; Gao, E.; Kalantari, S. EEG-based investigation of the impact of room size and window placement on cognitive performance. J. Build. Eng. 2022, 53, 104540. [Google Scholar] [CrossRef]
  112. Zhang, R.; Jia, J.; Zhang, R. EEG analysis of Parkinson’s disease using time–frequency analysis and deep learning. Biomed. Signal Process. Control 2022, 78, 103883. [Google Scholar] [CrossRef]
  113. Zhuang, Z.; Wang, F.; Yang, X.; Zhang, L.; Fu, C.H.; Xu, J.; Li, C.; Hong, H. Accurate contactless sleep apnea detection framework with signal processing and machine learning methods. Methods 2022, 205, 167–178. [Google Scholar] [CrossRef]
  114. Parhi, K.K.; Ayinala, M. Low-Complexity Welch Power Spectral Density Computation. IEEE Trans. Circuits Syst. I Regul. Pap. 2014, 61, 172–182. [Google Scholar] [CrossRef]
  115. Gore, E.; Rathi, S. Surveying Machine Learning Algorithms On Eeg Signals Data For Mental Health Assessment. In Proceedings of the 2019 IEEE Pune Section International Conference (PuneCon), Pune, India, 18–20 December 2019; IEEE: Pune, India, 2019; pp. 1–6. [Google Scholar] [CrossRef]
  116. Che Wan Fadzal, C.W.N.F.; Mansor, W.; Khuan, L.Y.; Mohamad, N.B.; Mahmoodin, Z.; Mohamad, S.; Amirin, S. Welch power spectral density of EEG signal generated from dyslexic children. In Proceedings of the 2014 IEEE REGION 10 SYMPOSIUM, Kuala Lumpur, Malaysia, 14–16 April 2014; IEEE: Kuala Lumpur, Malaysia, 2014; pp. 560–562. [Google Scholar] [CrossRef]
  117. Lai, D.; Heyat, M.B.B.; Khan, F.I.; Zhang, Y. Prognosis of Sleep Bruxism Using Power Spectral Density Approach Applied on EEG Signal of Both EMG1-EMG2 and ECG1-ECG2 Channels. IEEE Access 2019, 7, 82553–82562. [Google Scholar] [CrossRef]
  118. Kang, J.M.; Cho, S.E.; Moon, J.Y.; Kim, S.I.; Kim, J.W.; Kang, S.G. Difference in spectral power density of sleep electroencephalography between individuals without insomnia and frequent hypnotic users with insomnia complaints. Sci. Rep. 2022, 12, 2117. [Google Scholar] [CrossRef]
  119. Wang, L.; Deng, X.; Lv, X.; Liu, K.; Yang, Q.; Long, C. A WeChat Mini-program System with LSTM for The Emotional EEG Signal Recognition. In Proceedings of the 2020 2nd International Conference on Industrial Artificial Intelligence (IAI), Shenyang, China, 23–25 October 2020; IEEE: Shenyang, China, 2020; pp. 1–5. [Google Scholar] [CrossRef]
  120. Vuppalapati, C.; Raghu, N.; Veluru, P.; Khursheed, S. A System To Detect Mental Stress Using Machine Learning And Mobile Development. In Proceedings of the 2018 International Conference on Machine Learning and Cybernetics (ICMLC), Chengdu, China, 15–18 July 2018; IEEE: Chengdu, China, 2018; pp. 161–166. [Google Scholar] [CrossRef]
  121. You, Y.; Zhong, X.; Liu, G.; Yang, Z. Automatic sleep-stage classification: A light and efficient deep neural network model based on time, frequency and fractional Fourier transform domain features. Artif. Intell. Med. 2022, 127, 102279. [Google Scholar] [CrossRef]
  122. Zhang, Y.; Wang, K.; Wei, Y.; Guo, X.; Wen, J.; Luo, Y. Minimal EEG channel selection for depression detection with connectivity features during sleep. Comput. Biol. Med. 2022, 147, 105690. [Google Scholar] [CrossRef] [PubMed]
  123. Molin, N.L.; Molin, C.; Dalpatadu, R.J.; Singh, A.K. Prediction of obstructive sleep apnea using Fast Fourier Transform of overnight breath recordings. Mach. Learn. Appl. 2021, 4, 100022. [Google Scholar] [CrossRef]
  124. Chatterjee, R.; Bandyopadhyay, T.; Sanyal, D.K.; Guha, D. Dimensionality reduction of EEG signal using Fuzzy Discernibility Matrix. In Proceedings of the 2017 10th International Conference on Human System Interactions (HSI), Ulsan, Republic of Korea, 17–19 July 2017; IEEE: Ulsan, Republic of Korea, 2017; pp. 131–136. [Google Scholar] [CrossRef]
  125. Kadam, S.T.; Dhaimodker, V.M.; Patil, M.M.; Edla, D.R. EIQ: EEG based IQ test using wavelet packet transform and hierarchical extreme learning machine. J. Neurosci. Methods 2019, 322, 71–82. [Google Scholar] [CrossRef] [PubMed]
  126. Rodríguez-Bermúdez, G.; García-Laencina, P.J.; Roca-González, J.; Roca-Dorda, J. Efficient feature selection and linear discrimination of EEG signals. Neurocomputing 2013, 115, 161–165. [Google Scholar] [CrossRef]
  127. Zhang, J.; Yin, Z.; Chen, P.; Nichele, S. Emotion recognition using multi-modal data and machine learning techniques: A tutorial and review. Inf. Fusion 2020, 59, 103–126. [Google Scholar] [CrossRef]
  128. Adam, A.; Shapiai, M.I.; Mohd Tumari, M.Z.; Mohamad, M.S.; Mubin, M. Feature Selection and Classifier Parameters Estimation for EEG Signals Peak Detection Using Particle Swarm Optimization. Sci. World J. 2014, 2014, 973063. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  129. Debarnot, U.; Perrault, A.A.; Sterpenich, V.; Legendre, G.; Huber, C.; Guillot, A.; Schwartz, S. Motor imagery practice benefits during arm immobilization. Sci. Rep. 2021, 11, 8928. [Google Scholar] [CrossRef] [PubMed]
  130. Duan, L.; Ge, H.; Ma, W.; Miao, J. EEG feature selection method based on decision tree. Bio-Med. Mater. Eng. 2015, 26, S1019–S1025. [Google Scholar] [CrossRef] [Green Version]
  131. Duan, X.; Ying, S.; Yuan, W.; Cheng, H.; Yin, X. A Generative Adversarial Networks for Log Anomaly Detection. Comput. Syst. Sci. Eng. 2021, 37, 135–148. [Google Scholar] [CrossRef]
  132. Li, T.; Zhou, M. ECG Classification Using Wavelet Packet Entropy and Random Forests. Entropy 2016, 18, 285. [Google Scholar] [CrossRef]
  133. Utomo, O.K.; Surantha, N.; Isa, S.M.; Soewito, B. Automatic Sleep Stage Classification using Weighted ELM and PSO on Imbalanced Data from Single Lead ECG. Procedia Comput. Sci. 2019, 157, 321–328. [Google Scholar] [CrossRef]
  134. Annaby, M.; Said, M.; Eldeib, A.; Rushdi, M. EEG-based motor imagery classification using digraph Fourier transforms and extreme learning machines. Biomed. Signal Process. Control 2021, 69, 102831. [Google Scholar] [CrossRef]
  135. Wang, Y.; Wang, W.; Liu, Y.; Wang, D.; Liu, B.; Shi, Y.; Gao, P. Feature Extracting of Weak Signal in Real-Time Sleeping EEG with Approximate Entropy and Bispectrum Analysis. In Proceedings of the 2009 3rd International Conference on Bioinformatics and Biomedical Engineering, Beijing, China, 11–16 June 2009; IEEE: Beijing, China, 2009; pp. 1–4. [Google Scholar] [CrossRef]
  136. Koh, J.; Ooi, C.P.; Lim-Ashworth, N.S.; Vicnesh, J.; Tor, H.T.; Lih, O.S.; Tan, R.S.; Acharya, U.; Fung, D.S.S. Automated classification of attention deficit hyperactivity disorder and conduct disorder using entropy features with ECG signals. Comput. Biol. Med. 2022, 140, 105120. [Google Scholar] [CrossRef] [PubMed]
  137. Tautan, A.M.; Rossi, A.C.; de Francisco, R.; Ionescu, B. Automatic Sleep Stage Detection: A Study on the Influence of Various PSG Input Signals. In Proceedings of the 2020 42nd Annual International Conference of the IEEE Engineering in Medicine & Biology Society (EMBC), Montreal, QC, Canada, 20–24 July 2020; IEEE: Montreal, QC, Canada, 2020; pp. 5330–5334. [Google Scholar] [CrossRef]
  138. Zhou, D.; Xu, Q.; Wang, J.; Xu, H.; Kettunen, L.; Chang, Z.; Cong, F. Alleviating Class Imbalance Problem in Automatic Sleep Stage Classification. IEEE Trans. Instrum. Meas. 2022, 71, 1–12. [Google Scholar] [CrossRef]
  139. Efe, E.; Ozsen, S. CoSleepNet: Automated sleep staging using a hybrid CNN-LSTM network on imbalanced EEG-EOG datasets. Biomed. Signal Process. Control 2023, 80, 104299. [Google Scholar] [CrossRef]
  140. Xu, Q.; Zhou, D.; Wang, J.; Shen, J.; Kettunen, L.; Cong, F. Convolutional Neural Network Based Sleep Stage Classification with Class Imbalance. In Proceedings of the 2022 International Joint Conference on Neural Networks (IJCNN), Padua, Italy, 18–26 July 2022; IEEE: Padua, Italy, 2022; pp. 1–6. [Google Scholar] [CrossRef]
  141. Patterson, J.; Gibson, A. Deep Learning A Practitioner’s Approach; y O’Reilly Media, Inc.: Sebastopol, CA, USA, 2017. [Google Scholar]
  142. Qiu, S.; Zhao, H.; Jiang, N.; Wang, Z.; Liu, L.; An, Y.; Zhao, H.; Miao, X.; Liu, R.; Fortino, G. Multi-sensor information fusion based on machine learning for real applications in human activity recognition: State-of-the-art and research challenges. Inf. Fusion 2022, 80, 241–265. [Google Scholar] [CrossRef]
  143. Singh, P.; Singh, N.; Singh, K.K.; Singh, A. Chapter 5—Diagnosing of disease using machine learning. In Machine Learning and the Internet of Medical Things in Healthcare; Singh, K.K., Elhoseny, M., Singh, A., Elngar, A.A., Eds.; Academic Press: Cambridge, MA, USA, 2021; pp. 89–111. [Google Scholar] [CrossRef]
  144. Shehab, M.; Abualigah, L.; Shambour, Q.; Abu-Hashem, M.A.; Shambour, M.K.Y.; Alsalibi, A.I.; Gandomi, A.H. Machine learning in medical applications: A review of state-of-the-art methods. Comput. Biol. Med. 2022, 145, 105458. [Google Scholar] [CrossRef]
  145. Guo, K.; Mei, H.; Xie, X.; Xu, X. A Convolutional Neural Network Feature Fusion Framework with Ensemble Learning for EEG-based Emotion Classification. In Proceedings of the 2019 IEEE MTT-S International Microwave Biomedical Conference (IMBioC), Nanjing, China, 6–8 May 2019; IEEE: Nanjing, China, 2019; pp. 1–4. [Google Scholar] [CrossRef]
  146. Shatte, A.; Hutchinson, D.; Teague, S. Machine learning in mental health: A systematic scoping review of methods and applications. Psychol. Med. 2019, 49, 1426–1448. [Google Scholar] [CrossRef] [Green Version]
  147. Wang, J.; Chen, Y.; Hao, S.; Peng, X.; Hu, L. Deep learning for sensor-based activity recognition: A survey. Pattern Recognit. Lett. 2019, 119, 3–11. [Google Scholar] [CrossRef] [Green Version]
  148. Sathya, R.; Abraham, A. Comparison of Supervised and Unsupervised Learning Algorithms for Pattern Classification. Int. J. Adv. Res. Artif. Intell. 2013, 2, 1–80. [Google Scholar] [CrossRef] [Green Version]
  149. Schmidt, F.; Suri-Payer, F.; Gulenko, A.; Wallschlager, M.; Acker, A.; Kao, O. Unsupervised Anomaly Event Detection for Cloud Monitoring Using Online Arima. In Proceedings of the 2018 IEEE/ACM International Conference on Utility and Cloud Computing Companion (UCC Companion), Zurich, Switzerland, 17–20 December 2018; IEEE: Zurich, Switzerland, 2018; pp. 71–76. [Google Scholar] [CrossRef]
  150. Garcia-Ceja, E.; Riegler, M.; Nordgreen, T.; Jakobsen, P.; Oedegaard, K.J.; Tørresen, J. Mental health monitoring with multi-modal sensing and machine learning: A survey. Pervasive Mob. Comput. 2018, 51, 1–26. [Google Scholar] [CrossRef]
  151. Nash, C.; Nair, R.; Naqvi, S.M. Machine Learning and ADHD Mental Health Detection—A Short Survey. In Proceedings of the 2022 25th International Conference on Information Fusion (FUSION), Linköping, Sweden, 4–7 July 2022; IEEE: Linköping, Sweden, 2022; pp. 1–8. [Google Scholar] [CrossRef]
  152. Sarkar, A.; Singh, A.; Chakraborty, R. A deep learning-based comparative study to track mental depression from EEG data. Neurosci. Inform. 2022, 2, 100039. [Google Scholar] [CrossRef]
  153. Liu, F.T.; Ting, K.M.; Zhou, Z.H. Isolation-Based Anomaly Detection. ACM Trans. Knowl. Discov. Data 2012, 6, 1–39. [Google Scholar] [CrossRef]
  154. Moura, M.d.C.; Zio, E.; Lins, I.D.; Droguett, E. Failure and reliability prediction by support vector machines regression of time-series data. Reliab. Eng. Syst. Saf. 2011, 96, 1527–1534. [Google Scholar] [CrossRef]
  155. Stranges, S.; Tigbe, W.; Gómez-Olivé, F.X.; Thorogood, M.; Kandala, N.B. Sleep Problems: An Emerging Global Epidemic? Findings From the INDEPTH WHO-SAGE Study Among More Than 40,000 Older Adults From 8 Countries Across Africa and Asia. Sleep 2012, 35, 1173–1181. [Google Scholar] [CrossRef] [Green Version]
  156. Rajagopalan, S.S.; Bhardwaj, S.; Panda, R.; Reddam, V.R.; Ganne, C.; Kenchaiah, R.; Mundlamuri, R.C.; Kandavel, T.; Majumdar, K.K.; Parthasarathy, S.; et al. Machine learning detects EEG microstate alterations in patients living with temporal lobe epilepsy. Seizure 2018, 61, 8–13. [Google Scholar] [CrossRef] [Green Version]
  157. Thamaraimanalan, T.; Mohankumar, M.; Anandakumar, H.; Deepha, M.; Priya, U.H.; Priya, G.B.; Devi, M.A. Machine Learning based Patient Mental Health Prediction using Spectral Clustering and RBFN Algorithms. In Proceedings of the 2022 8th International Conference on Advanced Computing and Communication Systems (ICACCS), Coimbatore, India, 25–26 March 2022; IEEE: Coimbatore, India, 2022; pp. 1840–1843. [Google Scholar] [CrossRef]
  158. van der Velden, B.H.; Kuijf, H.J.; Gilhuijs, K.G.; Viergever, M.A. Explainable artificial intelligence (XAI) in deep learning-based medical image analysis. Med. Image Anal. 2022, 79, 102470. [Google Scholar] [CrossRef]
  159. Ahuja, R.; Banga, A. Mental Stress Detection in University Students using Machine Learning Algorithms. Procedia Comput. Sci. 2019, 152, 349–353. [Google Scholar] [CrossRef]
  160. He, Z.; Xu, X.; Deng, S. Discovering cluster-based local outliers. Pattern Recognit. Lett. 2003, 24, 1641–1650. [Google Scholar] [CrossRef]
  161. Hosseini, M.P.; Hosseini, A.; Ahi, K. A Review on Machine Learning for EEG Signal Processing in Bioengineering. IEEE Rev. Biomed. Eng. 2021, 14, 204–218. [Google Scholar] [CrossRef]
  162. Suthaharan, S. Support Vector Machine. In Machine Learning Models and Algorithms for Big Data Classification. Integrated Series in Information Systems; Springer: Boston, MA, USA, 2016; Volume 36. [Google Scholar]
  163. Khatun, S.; Morshed, B.I.; Bidelman, G.M. A Single-Channel EEG-Based Approach to Detect Mild Cognitive Impairment via Speech-Evoked Brain Responses. IEEE Trans. Neural Syst. Rehabil. Eng. 2019, 27, 1063–1070. [Google Scholar] [CrossRef] [PubMed]
  164. Raut, K.; Patil, J.; Wade, S.; Tinsu, J. Mental Health and Personality Determination using Machine Learning. In Proceedings of the 2022 7th International Conference on Communication and Electronics Systems (ICCES), Coimbatore, India, 22–24 June 2022; IEEE: Coimbatore, India, 2022; pp. 1231–1236. [Google Scholar] [CrossRef]
  165. Subhani, A.R.; Mumtaz, W.; Saad, M.N.B.M.; Kamel, N.; Malik, A.S. Machine Learning Framework for the Detection of Mental Stress at Multiple Levels. IEEE Access 2017, 5, 13545–13556. [Google Scholar] [CrossRef]
  166. Raj, A. The Perfect Recipe for Classification UsingLogistic Regression. Available online: https://towardsdatascience.com/the-perfect-recipe-for-classification-using-logistic-regression-f8648e267592 (accessed on 21 February 2023).
  167. Shen, C.; Lin, H.; Fan, X.; Chu, Y.; Yang, Z.; Wang, J.; Zhang, S. Biomedical event trigger detection with convolutional highway neural network and extreme learning machine. Appl. Soft Comput. 2019, 84, 105661. [Google Scholar] [CrossRef]
  168. Pawar, D.; Dhage, S. EEG-based covert speech decoding using random rotation extreme learning machine ensemble for intuitive BCI communication. Biomed. Signal Process. Control 2023, 80, 104379. [Google Scholar] [CrossRef]
  169. Cecaj, A.; Lippi, M.; Mamei, M.; Zambonelli, F. Comparing Deep Learning and Statistical Methods in Forecasting Crowd Distribution from Aggregated Mobile Phone Data. Appl. Sci. 2020, 10, 6580. [Google Scholar] [CrossRef]
  170. Guillot, A.; Sauvet, F.; During, E.H.; Thorey, V. Dreem Open Datasets: Multi-Scored Sleep Datasets to compare Human and Automated sleep staging. IEEE Trans. Neural Syst. Rehabilit. Eng. 2020, 28, 1955–1965. [Google Scholar] [CrossRef]
  171. Greff, K.; Srivastava, R.K.; Koutník, J.; Steunebrink, B.R.; Schmidhuber, J. LSTM: A Search Space Odyssey. IEEE Trans. Neural Netw. Learn. Syst. 2017, 28, 2222–2232. [Google Scholar] [CrossRef] [Green Version]
  172. Aydin, O.; Guldamlasioglu, S. Using LSTM networks to predict engine condition on large scale data processing framework. In Proceedings of the 2017 4th International Conference on Electrical and Electronic Engineering (ICEEE), Ankara, Turkey, 8–10 April 2017; IEEE: Ankara, Turkey, 2017; pp. 281–285. [Google Scholar] [CrossRef]
  173. Provotar, O.I.; Linder, Y.M.; Veres, M.M. Unsupervised Anomaly Detection in Time Series Using LSTM-Based Autoencoders. In Proceedings of the 2019 IEEE International Conference on Advanced Trends in Information Theory (ATIT), Kyiv, Ukraine, 18–20 December 2019; IEEE: Kyiv, Ukraine, 2019; pp. 513–517. [Google Scholar] [CrossRef]
  174. Shi, X.; Chen, Z.; Wang, H.; Yeung, D.Y.; Wong, W.k.; Woo, W.c. Convolutional LSTM Network: A Machine Learning Approach for Precipitation Nowcasting. In Proceedings of the 28th International Conference on Neural Information Processing Systems, Montreal, QC, Canada, 7–12 December 2015; p. 9. [Google Scholar]
  175. Vaswani, A.; Shazeer, N.; Parmar, N.; Uszkoreit, J.; Jones, L.; Gomez, A.N.; Kaiser, L.; Polosukhin, I. Attention Is All You Need. arXiv 2017, arXiv:1706.03762. [Google Scholar]
  176. Bhojanapalli, S.; Yun, C.; Rawat, A.S.; Reddi, S.; Kumar, S. Low-Rank Bottleneck in Multi-head Attention Models. In Proceedings of the 37th International Conference on Machine Learning, Virtual, 13–18 July 2020; pp. 864–873. [Google Scholar]
  177. Zhou, X.; Liang, W.; Wang, K.I.K.; Wang, H.; Yang, L.T.; Jin, Q. Deep-Learning-Enhanced Human Activity Recognition for Internet of Healthcare Things. IEEE Internet Things J. 2020, 7, 6429–6438. [Google Scholar] [CrossRef]
  178. Murad, A.; Pyun, J.Y. Deep Recurrent Neural Networks for Human Activity Recognition. Sensors 2017, 17, 2556. [Google Scholar] [CrossRef] [Green Version]
  179. Inoue, M.; Inoue, S.; Nishida, T. Deep recurrent neural network for mobile human activity recognition with high throughput. Artif. Life Robot. 2018, 23, 173–185. [Google Scholar] [CrossRef] [Green Version]
  180. Liu, L. Objects detection toward complicated high remote basketball sports by leveraging deep CNN architecture. Future Gener. Comput. Syst. 2021, 119, 31–36. [Google Scholar] [CrossRef]
  181. Hochreiter, S.; Schmidhuber, J. Long Short-Term Memory. Neural Comput. 1997, 9, 1735–1780. [Google Scholar] [CrossRef] [PubMed]
  182. Erdaş, Ç.B.; Güney, S. Human Activity Recognition by Using Different Deep Learning Approaches for Wearable Sensors. Neural Process. Lett. 2021, 53, 1795–1809. [Google Scholar] [CrossRef]
  183. Nath, R.K.; Thapliyal, H.; Caban-Holt, A. Machine Learning Based Stress Monitoring in Older Adults Using Wearable Sensors and Cortisol as Stress Biomarker. J. Signal Process. Syst. 2022, 94, 513–525. [Google Scholar] [CrossRef]
  184. Wu, N.; Green, B.; Ben, X.; O’Banion, S. Deep Transformer Models for Time Series Forecasting: The Influenza Prevalence Case. arXiv 2020, arXiv:2001.08317. [Google Scholar]
  185. Guillot, A.; Thorey, V. RobustSleepNet: Transfer Learning for Automated Sleep Staging at Scale. IEEE Trans. Neural Syst. Rehabil. Eng. 2021, 29, 1441–1451. [Google Scholar] [CrossRef]
  186. Munir, M.; Siddiqui, S.A.; Chattha, M.A.; Dengel, A.; Ahmed, S. FuseAD: Unsupervised Anomaly Detection in Streaming Sensors Data by Fusing Statistical and Deep Learning Models. Sensors 2019, 19, 2451. [Google Scholar] [CrossRef] [Green Version]
  187. Thongsuwan, S.; Jaiyen, S.; Padcharoen, A.; Agarwal, P. ConvXGB: A new deep learning model for classification problems based on CNN and XGBoost. Nucl. Eng. Technol. 2021, 53, 522–531. [Google Scholar] [CrossRef]
  188. Choi, S.H.; Yoon, H.; Kim, H.S.; Kim, H.B.; Kwon, H.B.; Oh, S.M.; Lee, Y.J.; Park, K.S. Real-time apnea-hypopnea event detection during sleep by convolutional neural networks. Comput. Biol. Med. 2018, 100, 123–131. [Google Scholar] [CrossRef]
  189. Kavi, R.; Kulathumani, V.; Rohit, F.; Kecojevic, V. Multiview fusion for activity recognition using deep neural networks. J. Electron. Imaging 2016, 25, 043010. [Google Scholar] [CrossRef]
  190. Hssayeni, M.D.; Jimenez-Shahed, J.; Burack, M.A.; Ghoraani, B. Ensemble deep model for continuous estimation of Unified Parkinson’s Disease Rating Scale III. Biomed. Eng. OnLine 2021, 20, 32. [Google Scholar] [CrossRef] [PubMed]
  191. Mutegeki, R.; Han, D.S. A CNN-LSTM Approach to Human Activity Recognition. In Proceedings of the 2020 International Conference on Artificial Intelligence in Information and Communication (ICAIIC), Fukuoka, Japan, 19–21 February 2020; IEEE: Fukuoka, Japan, 2020; pp. 362–366. [Google Scholar] [CrossRef]
  192. Mekruksavanich, S.; Jitpattanakul, A. LSTM Networks Using Smartphone Data for Sensor-Based Human Activity Recognition in Smart Homes. Sensors 2021, 21, 1636. [Google Scholar] [CrossRef] [PubMed]
  193. Na, Y.; Kim, D.; Kim, D.K.; Lee, J.G. Evaluation of OSA Patient Sleep Stage Classification Performance Using a Multi-Channel PSG Dataset. In Proceedings of the 2022 IEEE International Conference on Consumer Electronics-Asia (ICCE-Asia), Yeosu, Republic of Korea, 17–20 December 2022; IEEE: Yeosu, Republic of Korea, 2022; pp. 1–4. [Google Scholar] [CrossRef]
  194. Liu, Y.; Liu, H.; Yang, B. Automatic Sleep Arousals Detection From Polysomnography Using Multi-Convolution Neural Network and Random Forest. IEEE Access 2020, 8, 176343–176350. [Google Scholar] [CrossRef]
  195. Li, F.; Yan, R.; Mahini, R.; Wei, L.; Wang, Z.; Mathiak, K.; Liu, R.; Cong, F. End-to-end sleep staging using convolutional neural network in raw single-channel EEG. Biomed. Signal Process. Control 2021, 63, 102203. [Google Scholar] [CrossRef]
  196. Howe-Patterson, M.; Pourbabaee, B.; Benard, F. Automated Detection of Sleep Arousals From Polysomnography Data Using a Dense Convolutional Neural Network. In Proceedings of the 2018 Computing in Cardiology Conference (CinC), Maastricht, The Netherlands, 23–26 September 2018. [Google Scholar] [CrossRef]
  197. Yamazaki, K.; Vo-Ho, V.K.; Bulsara, D.; Le, N. Spiking Neural Networks and Their Applications: A Review. Brain Sci. 2022, 12, 863. [Google Scholar] [CrossRef] [PubMed]
  198. Doborjeh, Z.; Doborjeh, M.; Taylor, T.; Kasabov, N.; Wang, G.Y.; Siegert, R.; Sumich, A. Spiking Neural Network Modelling Approach Reveals How Mindfulness Training Rewires the Brain. Sci. Rep. 2019, 9, 6367. [Google Scholar] [CrossRef] [Green Version]
  199. Pfeiffer, M.; Pfeil, T. Deep Learning With Spiking Neurons: Opportunities and Challenges. Front. Neurosci. 2018, 12, 774. [Google Scholar] [CrossRef] [Green Version]
  200. Saputra, N.H.; Nafi’Iyah, N. Identification of Human Stress Based on EEG Signals Using Machine Learning. In Proceedings of the 2022 1st International Conference on Information System & Information Technology (ICISIT), Virtual, 27–28 July 2022; IEEE: Yogyakarta, Indonesia, 2022; pp. 176–180. [Google Scholar] [CrossRef]
  201. Bashar, K.; Chiaki, I.; Yoshida, H. Human identification from brain EEG signals using advanced machine learning method EEG-based biometrics. In Proceedings of the IEEE EMBS Conference on Biomedical Engineering and Sciences, Lyon, France, 4–8 December 2016; p. 5. [Google Scholar]
  202. Abdul Hamid, D.S.B.; Goyal, S.; Bedi, P. Integration of Deep Learning for Improved Diagnosis of Depression using EEG and Facial Features. Mater. Today Proc. 2021; in press. [Google Scholar] [CrossRef]
  203. Troncoso-García, A.; Martínez-Ballesteros, M.; Martínez-Álvarez, F.; Troncoso, A. Explainable machine learning for sleep apnea prediction. Procedia Comput. Sci. 2022, 207, 2930–2939. [Google Scholar] [CrossRef]
  204. Sharma, G.; Parashar, A.; Joshi, A.M. DepHNN: A novel hybrid neural network for electroencephalogram (EEG)-based screening of depression. Biomed. Signal Process. Control 2021, 66, 102393. [Google Scholar] [CrossRef]
  205. Acar, E. Unraveling Diagnostic Biomarkers of Schizophrenia Through Structure-Revealing Fusion of Multi-Modal Neuroimaging Data. Front. Neurosci. 2019, 13, 16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  206. Johnstone, S.J.; Parrish, L.; Jiang, H.; Zhang, D.W.; Williams, V.; Li, S. Aiding diagnosis of childhood attention-deficit/hyperactivity disorder of the inattentive presentation: Discriminant function analysis of multi-domain measures including EEG. Biol. Psychol. 2021, 161, 108080. [Google Scholar] [CrossRef] [PubMed]
  207. Bernardo, D.; Nariai, H.; Hussain, S.A.; Sankar, R.; Salamon, N.; Krueger, D.A.; Sahin, M.; Northrup, H.; Bebin, E.M.; Wu, J.Y. Visual and semi-automatic non-invasive detection of interictal fast ripples: A potential biomarker of epilepsy in children with tuberous sclerosis complex. Clin. Neurophysiol. 2018, 129, 1458–1466. [Google Scholar] [CrossRef] [PubMed]
  208. Mencar, C.; Gallo, C.; Mantero, M.; Tarsia, P.; Carpagnano, G.E.; Foschino Barbaro, M.P.; Lacedonia, D. Application of machine learning to predict obstructive sleep apnea syndrome severity. Health Inform. J. 2020, 26, 298–317. [Google Scholar] [CrossRef]
  209. Xu, D.; Wang, Y.; Meng, Y.; Zhang, Z. An Improved Data Anomaly Detection Method Based on Isolation Forest. In Proceedings of the 2017 10th International Symposium on Computational Intelligence and Design (ISCID), Hangzhou, China, 9–10 December 2017; IEEE: Hangzhou, China, 2017; pp. 287–291. [Google Scholar] [CrossRef]
  210. Satapathy, S.K.; Kondaveeti, H.K. Prognosis of Sleep Stage Classification Using Machine Learning Techniques Applied on Single-channel of EEG signal of both Healthy Subjects and Mild Sleep effected Subjects. In Proceedings of the 2021 International Conference on Artificial Intelligence and Machine Vision (AIMV), Gandhinagar, India, 28–30 June 2021; IEEE: Gandhinagar, India, 2021; pp. 1–7. [Google Scholar] [CrossRef]
  211. Zhu, G.; Li, Y.; Wen, P. Analysis and Classification of Sleep Stages Based on Difference Visibility Graphs From a Single-Channel EEG Signal. IEEE J. Biomed. Health Inform. 2014, 18, 1813–1821. [Google Scholar] [CrossRef]
  212. Salman, A.A.; Kumar, D.M.S. Introducing Confusion Matrix and Accuracy in Disease Prediction on Liver Using Machine Learning. Int. J. Comput. Sci. Trends Technol. (IJCST) 2020, 8, 5–9. [Google Scholar]
  213. Rahman, A.; Chowdhury, M.E.H.; Khandakar, A.; Kiranyaz, S.; Zaman, K.S.; Reaz, M.B.I.; Islam, M.T.; Kadir, M.A. Multimodal EEG and Keystroke Dynamics Based Biometric System Using Machine Learning Algorithms. IEEE Access 2021, 9, 19. [Google Scholar] [CrossRef]
  214. Zhou, D.; Wang, J.; Hu, G.; Zhang, J.; Li, F.; Yan, R.; Kettunen, L.; Chang, Z.; Xu, Q.; Cong, F. SingleChannelNet: A model for automatic sleep stage classification with raw single-channel EEG. Biomed. Signal Process. Control 2022, 75, 103592. [Google Scholar] [CrossRef]
  215. Kemp, B.; Olivan, J. European data format ‘plus’ (EDF+), an EDF alike standard format for the exchange of physiological data. Clin. Neurophysiol. 2003, 114, 1755–1761. [Google Scholar] [CrossRef]
  216. Korompili, G.; Amfilochiou, A.; Kokkalas, L.; Mitilineos, S.A.; Tatlas, N.A.; Kouvaras, M.; Kastanakis, E.; Maniou, C.; Potirakis, S.M. PSG-Audio, a scored polysomnography dataset with simultaneous audio recordings for sleep apnea studies. Sci. Data 2021, 8, 197. [Google Scholar] [CrossRef]
  217. Le Quy, T.; Roy, A.; Iosifidis, V.; Zhang, W.; Ntoutsi, E. A survey on datasets for fairness-aware machine learning. WIREs Data Min. Knowl. Discov. 2022, 12, e1452. [Google Scholar] [CrossRef]
  218. Ketola, E.C.; Barankovich, M.; Schuckers, S.; Ray-Dowling, A.; Hou, D.; Imtiaz, M.H. Channel Reduction for an EEG-Based Authentication System While Performing Motor Movements. Sensors 2022, 22, 39156. [Google Scholar] [CrossRef] [PubMed]
  219. Ng, C.R.; Fiedler, P.; Kuhlmann, L.; Liley, D.; Vasconcelos, B.; Fonseca, C.; Tamburro, G.; Comani, S.; Lui, T.K.Y.; Tse, C.Y.; et al. Multi-Center Evaluation of Gel-Based and Dry Multipin EEG Caps. Sensors 2022, 22, 8079. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Schematic diagram of the sleep stages according to EEG signals. The annotation was created according to RK standards and AASM recommendations for classifying sleep stages.
Figure 1. Schematic diagram of the sleep stages according to EEG signals. The annotation was created according to RK standards and AASM recommendations for classifying sleep stages.
Biomedinformatics 03 00014 g001
Figure 2. PRISMA Analysis of articles searched: Flow diagram for study collection and reviews, which included searching databases.
Figure 2. PRISMA Analysis of articles searched: Flow diagram for study collection and reviews, which included searching databases.
Biomedinformatics 03 00014 g002
Figure 3. Word cloud and bar graph of the titles of the articles used in this review.
Figure 3. Word cloud and bar graph of the titles of the articles used in this review.
Biomedinformatics 03 00014 g003
Figure 4. Word cloud and bar graph of all the abstracts of the articles used in this review.
Figure 4. Word cloud and bar graph of all the abstracts of the articles used in this review.
Biomedinformatics 03 00014 g004
Figure 5. Reviewed paper distribution by year of publication.
Figure 5. Reviewed paper distribution by year of publication.
Biomedinformatics 03 00014 g005
Figure 6. Overview of the process flow or steps of data preparation, feature extraction, ML modeling, and classification. Note the nomenclature section for abbreviations in the above process flow image. (a) Data Preparation [64]. (b) Feature Extraction [65]. (c) Machine-Learning Modeling [66]. (d) Validation.
Figure 6. Overview of the process flow or steps of data preparation, feature extraction, ML modeling, and classification. Note the nomenclature section for abbreviations in the above process flow image. (a) Data Preparation [64]. (b) Feature Extraction [65]. (c) Machine-Learning Modeling [66]. (d) Validation.
Biomedinformatics 03 00014 g006
Figure 7. EEG electrode placement locations [96].
Figure 7. EEG electrode placement locations [96].
Biomedinformatics 03 00014 g007
Figure 8. Flowchart of EEG signal pre-processing.
Figure 8. Flowchart of EEG signal pre-processing.
Biomedinformatics 03 00014 g008
Table 1. A summary of search criteria and results from the different digital databases.
Table 1. A summary of search criteria and results from the different digital databases.
Digital DatabaseSearch String UsedTotal Articles Collected
IEEE Xplore Access(“EEG” OR “ECG” OR “EOG” OR “EMG” OR “PSG”) AND “Machine Learning” AND “Mental Health”41
Science Direct(“EEG” OR “ECG” OR “EOG” OR “EMG” OR “PSG”) AND “Machine Learning” AND “Mental Health”944
MDPI(“EEG” OR “ECG” OR “EOG” OR “EMG” OR “PSG”) AND “Machine Learning” AND “Mental Health”26
PubMed(“EEG” OR “ECG” OR “EOG” OR “EMG” OR “PSG”) AND “Machine Learning” AND “Mental Health”76
Table 2. A summary of open-access PSG datasets. We presented basic information used by previous research in this field of study.
Table 2. A summary of open-access PSG datasets. We presented basic information used by previous research in this field of study.
DatasetDescriptionSource
Epileptic seizure developed by University of Bonn, GermanySampling frequency = 173.61 Hz; No. of persons = 5 (healthy) + 5 (Unhealthy); Total duration of a segment = 23.6 s; No. of trails/channels in a class = 100; Data size in this study = 200 × 4097[75]
Schizophrenia EEG dataset collected by the Institute of Psychiatry and Neurology in Warsaw, PolandSampling frequency = 250 Hz; No. of persons = 14 (healthy) + 14 (Unhealthy); Epoch size = 60 s × 250 Hz = 15,000; Data size in this study = [19 × (14 + 14)] × 15,000 = 532 × 15,000[75]
Sleep-EDF (S-EDF) (Scored by 1 sleep expert)Sampling frequency = 100 Hz; No. of persons = 8; Epoch length = 30 s; Data size = 15,139[29,38,76]
Sleep-EDF (Expanded) (SE-EDF) (Scored by 1 sleep expert)Sampling frequency = 100 Hz; No. of persons = 20 Epoch length = 30 s; Data size =40,100[29,38,76]
Laboratory for Neurophysiology and NeuroComputer Interfaces of M. V. Lomonosov Moscow State UniversitySampling frequency = 128 Hz; No. of persons= 45 (schizophrenic) + 39 (Normal); Data size = 16 × 7680; Matrix with 1344 instances[77]
The Epilepsy Ecosystem datasetSampling frequency = 400 Hz; No. of persons = 3[78]
The CHB-MIT datasetSampling frequency = 256 Hz; No. of persons = 23[78]
The BCI competition-II Dataset-IIISampling frequency = 128 Hz[79,80]
Test Set of SHHS1 Test Set of SHHS2Sampling frequency for ECG = 125 Hz in SHHS1 while ECG for SHHS2 = 250 Hz; No. of persons= 5793 for SHHS1 and 2651 for SHHS2[24,81,82]
MESA by National Sleep Research ResourceSampling frequency = 256 Hz for ECG; No. of persons = 2056[81,83]
The SLPDB databaseSampling frequency = 250 Hz; No. of persons = 16[81]
Apnea-ECG datasetSampling frequency = 128 Hz; No. of persons = 57 men + 13 women); Epoch length = 60 s; Segments = 17,045[82,84]
The MIT-BIH polysomnography datasetSampling frequency = 250 Hz; No. of persons = 16; Epoch length = 30 s[85]
The Massachusetts General Hospital (MGH Dataset) Sleep LaboratorySampling frequency = 200 Hz; Epoch length = 30 s[24]
DREAMER datasetSampling frequency = 128 Hz for EEG and 256 Hz for ECG No. of persons = 23[76,82,86,87]
Haaglanden Medisch Centrum Sleep Center Database (HMC)Sampling frequency = 256 Hz; No. of persons = 85 male + 66 female[82]
Sleep Telemetry Study (Telemetry)Sampling frequency = 200 Hz; No. of persons = 22 subjects (male and female)[82]
ISRUC-SLEEP dataset (ISRUC)Sampling frequency = 100 Hz; No. of persons = 100 subjects (55 male and 45 female)[82]
National Institute of Mental Health of the Czech Republic (NIMH-CZ).Sampling frequency = 250 Hz; No. of persons = 18[23]
DAIC-WOZ depression datasetSampling frequency = 16,000 Hz; No. of persons = 189 Subjects (54 % male and 46 % female )[5]
Montreal Archive of Sleep Studies (MASS)Sampling frequency = 256 Hz; No. of persons = 97 male + 103 female[69,88]
Department of Epileptology at Bonn UniversitySampling frequency = 256 Hz; No. of persons = 23 subjects[89]
Table 3. EEG waveform frequency band.
Table 3. EEG waveform frequency band.
BandsFrequency (Hz)Amplitude ( μ ν )Activities
Delta  ( δ ) 0–4.520–100Deep sleep
Theta  ( θ ) 4–810Light sleep
Alpha  ( α ) 8–132–100Calm or relaxed
Beta  ( β ) 15–225–10Alert
Gamma  ( γ ) >30-Hyperactive
Table 4. A summary of feature extraction methods for PSG data.
Table 4. A summary of feature extraction methods for PSG data.
Feature Extraction TechniquesSignal TypeReference
Adaptive auto-regressive (AAR)EEG-Motor-Imagery[79]
Adaptive auto-regressive
Fuzzy discernibility matrix (first adaptation)
EEG-Motor-Imagery[124]
Random asynchronous particle swarm optimizationEye Movement EEG[128]
Least angle regression + the direct leave-one-out error
estimation by the PRESS statistic
Motor-Imagery[129]
Principal component analysis + decision-tree-based feature
ranking (C4.5)
Motor-Imagery[129,130,131]
Wavelet packet decomposition + approximation entropy +
one-dimensional real-valued particle-swarm optimization
Motor-Imagery, Emotional Recognition[132,133]
Common spatial model (CSP)Motor-Imagery[134]
Discrete wavelet decomposition (DWT) in five frequency bands,
combined with wavelet entropy
Motor-Imagery, Emotional Recognition[21,76,135]
Differential entropy (DE)Motor-Imagery[136]
Table 5. A summary of machine learning-based studies for classification and prediction of PSG data.
Table 5. A summary of machine learning-based studies for classification and prediction of PSG data.
ModelApplicationData UsedAccuracyYear Ref.
LREEG abnormalities of micro-states in temporal lobe epilepsy (TLE)Privately sourced dataset from a tertiary institute66.70%2018 [156]
Mental depression from EEG datasetemotions.csv available on the Kaggle website96.60%2022 [152]
Emotion RecognitionDREAMER (discrete emotion recognition)94.49%2021 [86]
KNNEGG, (stress and emotion classification 97.00%2022 [200]
Obstructive sleep apnea (OSA), ECG and SPO2 signalsPhysioNet Sleep Apnea Database95.08%2017 [71]
SVMEEG image data and emotion classificationSEED dataset56.00%2022 [99]
Obstructive sleep apnea (OSA), ECG and SPO2 signalsPhysioNet Sleep Apnea Database96.64%2017 [71]
EEG sleep qualitySleep-EDF Database91.40%2019 [28]
Imaging and EEG data for ADHDADHD-200 dataset97.60%2022 [151]
Human recognition EEGEMOTIV INSIGHT dataset94.44%2016 [201]
mental stress detection using EEG signalmental arithmetic tasks database97.26%2022 [56]
EEG-dimensionality reductionDataset III of BCI competition II81.40%2017 [124]
motor imagery EEG signalThe BCI competition-II Dataset-III78.57%2019 [79]
Identification of chronic alcohol users from ECG signalsNIMHANS- ECG dataset87.50%2017 [43]
Sleep quality measurementSleep-EDF Database93.50%2019 [28]
Mental depression from EEG datasetemotions.csv available on the Kaggle website95.89%2022 [152]
Detection of schizophrenia from EEG dataEEG dataset from NNCI M. V. Lomonosov Moscow State University53.50%2022 [77]
ResNet-50EEG image data and emotion classificationSEED Dataset85.11%2022 [99]
CNNEEG-sleep stage using multi-scale dual-attentionSleep-EDF Database96.70%2022 [29]
Mental depression from EEG datasetemotions.csv available on the Kaggle website49.82%2022 [152]
Automatic sleep scoringMultiple EGG dataset was used for this work74.17%2021 [82]
Emotion recognitionDREAMER (discrete emotion recognition)99.90%2021 [86]
ELMIdentification of chronic alcohol users from ECG signalsNIMHANS- ECG Dataset94.64%2017 [43]
MLPMental depression from EEG datasetemotions.csv available on the Kaggle website76.43%2022 [152]
RNNMental depression from EEG datasetemotions.csv available on the Kaggle website93.90%2022 [152]
RNN with LSTMMental depression from EEG datasetemotions.csv available on the Kaggle website97.65%2022 [152]
Detection of schizophrenia from EEG DataEEG dataset from NNCI M. V. Lomonosov Moscow State University98.00%2022 [77]
Insomnia detectionMASS Dataset-EEG, EOG, EMG, ECG, and respiratory signals79.20%2021 [88]
Depression using EEGBCI project for EEG signal and frontal facial data99.66%2021 [202]
CNN–LSTMAutomatic sleep scoringMultiple EGG dataset was used for this work80.17%2021 [82]
Sleep apneaApnea-ECG dataset97.21%2022 [84]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Ehiabhi, J.; Wang, H. A Systematic Review of Machine Learning Models in Mental Health Analysis Based on Multi-Channel Multi-Modal Biometric Signals. BioMedInformatics 2023, 3, 193-219. https://doi.org/10.3390/biomedinformatics3010014

AMA Style

Ehiabhi J, Wang H. A Systematic Review of Machine Learning Models in Mental Health Analysis Based on Multi-Channel Multi-Modal Biometric Signals. BioMedInformatics. 2023; 3(1):193-219. https://doi.org/10.3390/biomedinformatics3010014

Chicago/Turabian Style

Ehiabhi, Jolly, and Haifeng Wang. 2023. "A Systematic Review of Machine Learning Models in Mental Health Analysis Based on Multi-Channel Multi-Modal Biometric Signals" BioMedInformatics 3, no. 1: 193-219. https://doi.org/10.3390/biomedinformatics3010014

APA Style

Ehiabhi, J., & Wang, H. (2023). A Systematic Review of Machine Learning Models in Mental Health Analysis Based on Multi-Channel Multi-Modal Biometric Signals. BioMedInformatics, 3(1), 193-219. https://doi.org/10.3390/biomedinformatics3010014

Article Metrics

Back to TopTop