Classification of Normal, Ictal and Inter-ictal EEG via Direct Quadrature and Random Forest Tree


This paper presents an accurate nonlinear classification method that can help physicians diagnose seizure in electroencephalographic (EEG) signal characterized by a disturbance in temporal and spectral content. This is accomplished by applying four steps. First, different EEG signals containing healthy, ictal and seizure-free (inter-ictal) activities are decomposed by empirical mode decomposition method. The instantaneous amplitudes and frequencies of resulted bands (intrinsic mode functions, IMF) are then tracked by the direct quadrature method (DQ). In contrast to other approaches, DQ cancels the effect of amplitude modulation on frequency calculation. The dissociation between instantaneous amplitude and frequency information is therefore fully achieved to avoid features confusion. Afterwards, the Shannon entropy values of both sets of instantaneous values (amplitudes and frequencies)—related to every IMF—are calculated. Finally, the obtained entropy values are classified by random forest tree. The proposed procedure yields 100% accuracy for (healthy)/(ictal) and 98.3–99.7% for (healthy)/(ictal)/(interictal) classification problems. The suggested method is hence robust, accurate, fast, user-friendly, data driven with open access interpretability.


Electroencephalography (EEG) is a medical technique that reads scalp electrical activity generated by brain structures. It is an accurate tool for identification of various types of abnormalities in brain. Epilepsy seizure is one of those complex abnormalities detected by EEG. It is a disturbed electrochemical release in a large cell population. That affects the quality of life of the patient, causing social impairment and a higher risk of death [1]. The spectral and temporal content analysis of EEG signals provides helpful information about the nature of seizure. However, the tool of analysis applied to EEG must be adapted to the characteristics of non-stationary non-linear brain activities.

Several approaches have been applied to EEG signals with the intention of identification of normal, ictal and inter-ictal activities; the latter of which being seizure-free segments occurring between seizure (ictal) fragments. The studies utilize time-domain, frequency-domain, time–frequency and spatial features [2, 3]. In [4], a difference in the synchronization level has been observed between EEG seizure and seizure-free intervals. The seizure EEG signals were found to be less random, more nonlinear-dependent, more stationary with comparatively different amplitude level [5,6,7,8,9]. Consequently, every tool utilised for seizure pattern recognition should have the capability to take these main variations into account. In [10], empirical mode decomposition (EMD) [11] has been employed to extract the inherent sub-bands (intrinsic mode functions, IMF) of a number of EEG signals. The mean frequencies of the resulted IMFs are then computed from the Fourier–Bessel series and used as the main features of classification. In the works of [1, 12,13,14,15,16,17,18,19,20,21], EMD has also been used as the first step. Nonetheless, the exploited features are different. The authors exploited a variety of parameters related to the obtained IMFs: the mean frequencies calculated by Hilbert Transform, the local patterns, the variation coefficients, the fluctuation indices, the entropy measures, the area calculated from the analytic signals, difference plots and phase space representations. In [22], EEG sub-bands have been realized by filtering. Approximate entropy values are subsequently calculated. In [23,24,25,26], Wavelet Transform (WT) has been the chosen method for sub-bands calculation. In [27,28,29], entropy values of EEG components, found by WT, were selected as classification features. In [30], fractional energy on specific Short-Fourier Transform windows has been the feature used for seizure classification. In [31], approximate entropy of EEG amplitude values has been calculated and classified using neural networks. The authors of [32] exploited the properties of Fast Fourier Transform to classify epileptiform EEG using decision tree classifier. In [33], fractional energy values of EEG components, found by pseudo-Wigner–Ville distribution, have been classified via neural networks. In [34], Lyapunov exponents of EEG signals have been utilized as features serving for seizure pattern recognition. The last step in all of the previous studies is the statistical processing of extracted features in order to attempt seizure pattern recognition. Various methods have been applied: nearest neighbour classifiers, decision trees, neural networks, support vector machines, and adaptive neuro-fuzzy systems [33].

The processing of seizure segments necessitates a tool that can adapt to EEG non-stationary and non-linear characteristics and does not imply pre-models [10, 13, 14]. Fourier Transform assumes stationary characteristics. Short-Fourier (SFT) and Wavelet Transforms (WT) assume linear properties as indicated by the first author of the present work in [35]. Furthermore, involving a specific mother wavelet in EEG processing implies a pre-model for analysis and spectral/time resolution. Investigations based on SFT and WT should therefore be complex enough in order to compensate the points of weakness and to turn into data-driven. On the other hand, nonlinear empirical mode decomposition can adaptively and intuitively represent non-stationary signals as sums of zero-mean locally symmetric mono-components AM–FM components (IMFs) [11]. The extracted components are speculatively associated with specific physiological aspects of the phenomenon investigated. EMD method is data driven, intuitive, not time consuming, does not need a predefined model and does not involve concepts of frequency or time resolution.

As indicated, a number of studies have exploited the advantages of EMD for EEG seizure analysis. The highest obtained accuracy values were found when both local temporal and spectral features were utilized [12]. However, the effect of temporal amplitude modulation on extracted spectral features leaded to a reduction of accuracy. In the present paper, direct quadrature (DQ) method is applied to EEG IMFs in order to extract instantaneous amplitudes and frequencies features. In contrast to other approaches, DQ cancels the effect of amplitude modulation on frequency calculation. The dissociation between instantaneous amplitude and frequency information is therefore fully achieved to avoid features confusion. Shannon entropy values of resulted instantaneous values are subsequently calculated.

Open-interpretability and fast processing are essential characteristics that should be included by every EEG seizure analyzer. The highest classification accuracy values have been obtained in previous works [25, 33] when neural networks were exploited. However, the inherent classifier pathways in neural networks are relatively “Black boxes” with slow algorithms. Forest random tree is therefore utilized in the present work for features classification. In contrast to neural networks, transparency of tree classifier is important advantage that can help physicians understand the underlying mechanisms in seizure. Furthermore, fast treatment is a promising benefit for eventual seizure prediction.

Materials and Methods

The overall procedure of the present work is illustrated in Fig. 1. EEG signals (normal, ictal and inter-ictal) are decomposed by EMD. Resulted IMF are then analyzed by direct quadrature method in order to calculate instantaneous amplitudes and frequencies. Shannon entropy of issued instantaneous values are then classified by random forest tree. Finally, classification results are statistically assessed. In the following sections, details about used EEG dataset, decomposition, direct quadrature elements, entropy calculation, feature classification and statistical assessments, respectively, are presented.

Fig. 1

Suggested steps of EEG signals classification


The EEG dataset presented in [36] is used. The data set includes single channel EEG from healthy and epileptic subjects. The data has five subsets denoted as A_Z, B_O, C_N, D_F and E_S, each containing 100 single channel recordings, each one having 23.6 s in duration. The sampling frequency of the data is 173.61 Hz. The subsets A_Z and B_O have been recorded extra-cranially. They have been acquired using surface EEG recordings of five healthy volunteers with eyes open and closed respectively. Subsets D_F and C_N have been measured in seizure-free intervals from five patients in epileptic zone and from hyppocampal formation of opposite hemisphere of the brain, respectively. The subset E_S contains seizure activity selected from all recording sites exhibiting ictal activity [12]. The data bandwidth is [0.5–85] Hz. In the present paper, the subsets A_Z, C_N, D_F and E_S are used.


EMD, developed in [11], is a method applied to extract all the oscillatory modes (IMF) embedded in a signal in non-stationary or non-linear conditions. It is data driven, has no difficulties associated with resolution issues and its extracted modes are related to inherent processes. In every extracted IMF, the maximum allowed difference between the number of extrema and the number of zero crossings is one. Besides, the local average of the upper and lower envelopes is zero. These properties permit subsequent calculation of instantaneous frequency and amplitude. The sifting process for extracting IMFs from a signal consists of: first, the identification of all of the maxima and minima. Second, the generation of upper and lower envelopes by cubic spline interpolation and the calculation of point-by-point mean from the envelopes. Third, the extraction of the detail which is the result of subtraction of the obtained point-by-point mean from the signal. The detail should satisfy the two previously mentioned IMF properties in order to be considered as an IMF. Fourth, the replacement of the original signal with the residual (signal-detail); it is to be considered as the signal for the subsequent IMF calculation. However, if the detail does not meet the requirements, the steps 1–3 should be repeated (iterated) and applied to the detail until it satisfies the two criteria. Finally, the original signal can be expressed as the summation of all of the resulted amplitude modulated-frequency modulated (AM–FM) details and the final residual.

In the present paper, decomposition of used EEG signals has been realized by MATLAB. The maximum number of sifting iterations is 2000.

Direct Quadrature

The DQ [37] principle is based on the separation of the two effects of amplitude and frequency modulation. Normalization helps remove the effect of amplitude modulation in order to measure the correct instantaneous frequency by the Hilbert transform. Amplitude normalization is performed relative to the envelope of the IMF considered as given by the following equation:

$$f_{1} (k) = \frac{IMF(k)}{{e_{1} (k)}};f_{2} (k) = \frac{{f_{1} (k)}}{{e_{2} (k)}} \cdots f_{n} (k) = \frac{{f_{n - 1} (k)}}{{e_{n} (k)}}$$

where n is the number of normalizations performed. The term IMF (k) represents the kth sample of IMF. f n (k) is the frequency modulated component. e n (k) is the envelope passing through the maxima of absolute values of f n−1 (k) and conducted by the same approach used to calculate the envelope in EMD. The selected number of successive normalizations n in the present work is 5. Hilbert transform can then be calculated in order to find the correct instantaneous frequency and amplitude [12]. The proposed method is applied by MATLAB to all IMFs resulted from every EEG signal decomposition. Instantaneous frequency and amplitude values can be found by Hilbert transform [38, 39] as the instantaneous pulsation and amplitude of the complex analytic signal. The imaginary part of the analytic signal can be calculated by the following formula:

$$y(t) = \frac{1}{\pi }\mathop {\lim }\limits_{{ \in \to 0^{ + } }} \left( {\int\limits_{t - 1/ \in }^{t - \in } {\frac{x(\tau )}{t - \tau }d\tau } + \int\limits_{t + \in }^{t + 1/ \in } {\frac{x(\tau )}{t - \tau }d\tau } } \right)$$

where x(t) is the resulted IMF and is considered as the real part.

Shannon Entropy

Shannon entropy is given by:

$$H = - \sum\limits_{i} {p_{i} \log_{b} p_{i} }$$

where pi is the probability of a value i showing up in a stream of data. Shannon entropy values of the resulted instantaneous frequencies and amplitudes, of the IMFs issued from all used EEG signals, have been calculated by MATLAB.

Classification and Validation

The classification has been realized by Forest Random tree [40] and k-fold stratified cross-validation approaches via WEKA (Waikato Environment for Knowledge Analysis) software. A random tree considers randomly a number of chosen attributes at each node. In k-fold cross-validation, the original sample is randomly partitioned into k equal sized subsamples. Of the k subsamples, a single subsample is retained as the validation data for testing the model, and the remaining k − 1 subsamples are used as training data. The cross-validation process is then repeated k times (the folds), with each of the k subsamples used exactly once as the validation data. The k results from the folds can then be averaged (or otherwise combined) to produce a single estimation. In stratified k-fold cross-validation, the folds are selected so that the mean response value is approximately equal in all the folds. The main reason for using cross-validation instead of using the conventional validation (e.g. partitioning the data set into two sets of 70% for training and 30% for test) is that the root mean square error on the training set in the conventional validation is not a useful estimator of model performance and thus the error on the test data set does not properly represent the assessment of model performance [41]. Cross-validation combines (averages) measures of fit (prediction error) to correct for the optimistic nature of training error and derive a more accurate estimate of model prediction performance [42]. Cross validation yields a confusion matrix that indicates true positive, true negative, false positive, false negative rates for every class. The following three types of pattern recognition have been carried out:

Healthy/ictal Recognition

A number of 200 signals from A_Z and E_S (100 signals from every dataset) have been used. As every signal has been decomposed into N IMFs, the total number of IMFs is 200 * N. Every IMF has its related calculated instantaneous frequencies and amplitudes for which entropy values are calculated. The features matrix has therefore a dimension of (200 * 2 * N). The matrix entries have been classified into two classes: normal and ictal. Classification is achieved by Forest Random tree with 40 unlimited depth trees and tenfold cross-validation.

Healthy/Ictal/Inter-ictal (F) Recognition

A number of 300 signals from A_Z, E_S and D_F (100 signals from every dataset) have been used. As every signal has been decomposed into N IMFs, the total number of IMFs is 300 * N. The features matrix has therefore a dimension of (300 * 2 * N). The sub-matrices related to numbers of investigated IMFs scales ranging from 1 to N − 1 have also been examined. Each sub-matrix has been classified into three classes: normal, ictal and inter-ictal (epileptic zone). Classification is achieved by Forest Random tree and tenfold cross-validation with 30 unlimited depth trees.

Healthy/Ictal/Inter-ictal (F), Inter-ictal (N) Recognition

A number of 400 signals from A_Z and E_S, D_F and C_N have been used. As every signal has been decomposed into N IMFs, the total number of IMFs is 400 * N. The features matrix has therefore a dimension of (400 * 2 * N). The matrix entries have been classified into three classes: normal, ictal and inter-ictal (epileptic zone) with inter-ictal (opposite hemisphere). Classification is achieved by Forest Random tree with 30 unlimited depth trees and 20-fold cross-validation.

Attribute Selection

The contribution weight of features is studied by WEKA to find the most significant features. CFS supervised attribute subset evaluator (selector) has been used with simple genetic search. Crossover probability, number of generations and mutation probability values are 0.6, 20 and 0.033, respectively. Attribute selector evaluates the worth of a subset of attributes by considering the individual predictive ability of each feature along with the degree of redundancy between them. Subsets of features that are highly correlated with the class while having low inter-correlation are preferred. It identifies locally predictive attributes and iteratively adds attributes with the highest correlation with the class as long as there is not already an attribute in the subset that has a higher correlation with the attribute in question. It treats missing as a separate value. The attribute selection mode is a tenfold stratified cross validation.

Classification Assessment

Statistical assessment has been conducted by MedCalc based on resulted confusion matrix—issued from cross validation—in order to evaluate the obtained classification results. The calculated statistical descriptors are: accuracy, sensitivity, specificity, positive likelihood ratio, negative likelihood ratio, class prevalence, positive predictive value and negative predictive value using the formula of the Bayes’ theorem as follows below, where a: true positive, b: false negative, c: false positive and d: true negative. In the case of our studied classification problem, the unit of a, b, c and d is ‘EEG signal’. For example, if ‘a’ is 5, it means that 5 EEG signals are correctly classified in a specific class.

$${\text{Sensitivity:}}\quad \frac{a}{a + b}$$
$${\text{Specificity:}}\quad \frac{d}{c + d}$$
$${\text{Positive}}\;{\text{Likelihood}}\;{\text{Ratio:}}\quad \frac{Sensitivity}{100 - Specificity}$$

The PLR value is undefined when specificity is 100%. In this case, the cell related to positive likelihood ratio value (in the tables of results section) will not be filled.

$${\text{Negative}}\;{\text{likelihood}}\;{\text{ratio:}}\quad \frac{100 - Sensitivity}{Specificity}$$
$${\text{Class}}\;{\text{prevalence:}}\quad \frac{a + b}{a + b + c + d}$$
$${\text{Positive}}\;{\text{predictive}}\;{\text{value:}}\quad \frac{a}{a + c}$$
$${\text{Negative}}\;{\text{predictive}}\;{\text{value:}}\quad \frac{d}{b + d}$$

The above values are dimensionless. However, in the results section, they will be presented after multiplication by 100%.

The statistical evaluation of the classification is achieved for every class. Evaluation for a certain class is conducted if it is considered as the target. Multiple values for every statistical descriptor have therefore been calculated; every value corresponds to the evaluation of one class.

Results and Discussion

Figure 2 illustrates an example of IMFs issued from EMD decomposition. It shows IMFs resulted from EMD of a signal in the dataset F (inter-ictal). The first IMFs include noise and fast waves. The last IMFs include baseline and slow waves. As indicated above, the synchronization and amplitude levels in normal EEG differ from epileptic signals. This information is inherent in IMFs temporal and spectral contents. Consequently, in the present work, all IMFs scales are taken into account in subsequent classification in order to examine the maximum temporal and spectral information level. It is noteworthy that not all of the decomposed investigated signals gave the same number of IMFs. Inter-ictal signals yielded higher number of scales than ictal and normal ones. However, all signals achieved a number within the range (8–14). Fourteen is therefore considered the maximum number taken into account. For signals yielding a number less than 14, entropy values based on empty IMFs are considered as missing values. Random Forest classifier is one of the classifiers that have the capability to deal with this case.

Fig. 2

IMFs issued from EMD decomposition of a signal from the inter-ictal dataset F

Table 1 illustrates a sample of entropy values of instantaneous frequencies and amplitudes for the different classes. For space reasons we have limited the values to the tenth scale. The calculated values are based on the analytic signals of IMFs after applying the DQ normalization. Absolute value of entropy decreases in slow wave IMFs.

Table 1 A sample of entropy values of instantaneous frequencies and amplitudes for the different IMFs scales and classes

Healthy/ictal Recognition

All of the normal and ictal instances have been correctly classified by the proposed method. The overall accuracy is therefore 100%. Hence, the sensitivity and the specificity attain 100%. Table 2 summarizes the outcomes of the normal/ictal classification.

Table 2 Results of classification (normal/ictal EEG)

The obtained accuracy is equal to the highest value achieved in previous literature [33] using the same EEG database as indicated in Table 3. However, EMD is nonlinear, empirical, intuitive and simpler than the exploited methods that have leaded to accuracy up to 100%. Wigner–Ville distribution used in [33] achieved 100% but was not perfectly adapted to non-linear situations. The manipulation of time windows, frequency sub-bands and resolution was therefore lengthy, imposed and not data driven. Trial-and-error based resolution and scale selection was also a disadvantage. In addition, the methods previously investigated in literature and leading to high accuracy of normal/ictal classification yield noticeably a lower accuracy when they are applied to normal/ictal/inter-ictal classification [43].

Table 3 Results of classification (normal/ictal EEG) in literature using the same EEG database

Although the works in [10, 12] bring into play the strong characteristics of EMD, they achieved lower accuracies than 100% due to the effect of temporal amplitude modulation of IMFs on spectral information calculation. In the present paper, the elimination of this disadvantage helped increase the accuracy to 100%.

Healthy/Ictal/Inter-ictal (F) Recognition

According to the resulted confusion matrix, in the second classification problem, all normal and ictal instances are correctly classified. 99 out of 100 inter-ictal signals are accurately classified, as indicated in Table 4. The missed instance has been misclassified as ictal. The overall accuracy is therefore 99.7%. It is higher than the accuracy values found out by other approaches utilizing the same dataset, as indicated in Table 5. This is due to the fact that Direct Quadrature method is a reliable technique that helps acquire pertinent amplitude and frequency features without overlap or redundancy. The temporal and spectral information inherent in seizure spikes is consequently represented decently by features vector.

Table 4 Results of classification (normal/ictal/inter-ictal EEG)
Table 5 Results of classification (normal/ictal/inter-ictal EEG) in literature using the same EEG database

Table 6 shows the achieved classification accuracies versus number of investigated IMFs. The outcomes demonstrate that the accuracy depends on the number of exploited IMFs. The highest accuracy is achieved when 14 IMFs are taken into account. This might explain the lower accuracies achieved in literature utilizing smaller number of IMFs [10, 12, 33]. However, close accuracy (99.3%) is obtained when the number of selected IMFs is 5. The outcome of normal/ictal classification varies slightly versus numbers of IMFs higher than 5. According to the results, the IMFs containing lower frequencies are also relatively informative about features distinguishing between normal, ictal and inter-ictal. In a previous work conducted by the first author [12], only the first four IMFs were taken into account. However, the obtained accuracy was lower (94%).

Table 6 Result of classification (normal/ictal/inter-ictal (F) EEG) versus number of IMFs taken into account in classification

According to the applied CFS attribute evaluator with genetic search, the features having high predictive ability are f1, f2, a1, a2, a3, a4 and a5. Relative contribution of every feature is illustrated in Fig. 3. The found weights of contribution of features are consistent with the findings in Table 6.

Fig. 3

Relative contribution of every feature

Significance of high-contribution features can also be illustrated in Fig. 4a–e that present the 2-D distribution (frequency entropy, amplitude entropy) for the scales 1, 2, 3, 4 and 5, respectively. Basically, three primary clusters can be seen in every scale.

Fig. 4

a 2-D distribution of entropy values for IMFs of scale 1 (blue normal, red ictal, green inter-ictal). X-axis frequency entropy. Y axis amplitude entropy. b 2-D distribution of entropy values for IMFs of scale 2 (blue normal, red ictal, green inter-ictal). X-axis frequency entropy. Y-axis amplitude entropy. c 2-D distribution of entropy values for IMFs of scale 3 (blue normal, red ictal, green inter-ictal). X-axis frequency entropy. Y-axis amplitude entropy. d 2-D distribution of entropy values for IMFs of scale 4 (blue normal, red ictal, green inter-ictal). X-axis frequency entropy. Y-axis amplitude entropy. e 2-D distribution of entropy values for IMFs of scale 5 (blue normal, red ictal, green inter-ictal). X-axis frequency entropy. Y-axis amplitude entropy

It can be illustrated from Fig. 4a–e that, in all scales from 1 to 5, the amplitude entropy cluster centre of the IMFs resulted from ictal signals is higher than those of normal and inter-ictal. However, the difference is not obvious between the values of amplitude entropy of normal and inter-ictal clusters. These findings are consistent with Fig. 3 where the weights of a1–a5 are relatively high. On the other hand, in the high frequency scales 1–3, centres of frequency entropy values differ between clusters of normal and inter-ictal IMFs as well as between clusters of ictal and inter-ictal IMF. These findings are consistent with Fig. 3 where the weights of f4 and f5 are small compared to f1, f2 and f3. The results illustrated for all clusters are also compatible with the pace of increasing of accuracies, versus number of IMFs, presented in Table 6.

Healthy/Ictal/Inter-ictal (F), Inter-ictal (N) Recognition

The EEG recordings from seizure-free intervals can also be used to study the changes in the underlying dynamics of the cortex affected by epilepsy. The achieved accuracy of healthy/ictal/inter-ictal (F), inter-ictal (N) classification is 98.3% as shown by Table 7. Used method is Random forest of 30 trees, each constructed while considering five random features. The obtained accuracy is higher than the accuracy values found out by other approaches utilizing the same dataset, as indicated in Table 5. According to the resulted confusion matrix, 99 normal instances have been correctly classified. One normal instance has been misclassified as inter-ictal. 97 ictal instances have been correctly classified. Three ictal instances have been misclassified as inter-ictal. 197 inter-ictal instances have been correctly classified. Two inter-ictal instances have been misclassified as normal. One inter-ictal instance has been misclassified as ictal.

Table 7 Results of classification (normal/ictal/inter-ictal (F), inter-ictal (N) EEG)

The present work has many advantages. It leads to fast, low computational cost and user-friendly processing. The proposed method leads to high accuracy in comparison to other methods in literature. Furthermore, the obtained accuracy does not fall abruptly when the classification problem includes more than two classes or EEG issued from different seizure zones. The method is therefore more robust and easy-to-use than several techniques, as shown in the previous sections.

EMD application to EEG does not imply the knowledge of a priori temporal/spectral information about the signals. It is intuitively driven by the nature of the decomposed EEG time series [62]. Consequently, it does not analyze ictal, inter-ictal and normal segments by the same “Model”. On the other hand, conventional time–frequency decomposition tools involve a priori assumptions that lead to pre-models insensitive to differences between epileptic signals.

EMD is not critically parameter dependent. Moreover, spectral resolution and number of achieved scales of decomposition are empirically defined, based on the inherent physiology of analyzed EEG. On the other hand, scales in Wavelet or Fourier derived transforms should be pre-defined. Pre-definition of scales might result in missing or skipping important information/features.

In the present work, not all issued IMFs are purely mono-components. Amplitude and frequency modulation induce therefore a difficulty of instantaneous analysis. However, Direct Quadrature method overcomes the problem by the normalization system. Robust and precise calculation of features, based on accurate instantaneous values, is the main advantage of the suggested procedure.

The used random forest tree classifier is a fast tool with the advantage of open-access interpretability. Neural networks NN used in studies yielding relatively good accuracies are slower “black boxes” that do not permit easy interpretation of inherent physiological processes. Furthermore, NN imply the determination of a number of sensitive parameters values on which outcome is highly dependent.

The results of feature selection illustrate the weight of every IMF in the overall analysis as well as the significance of related temporal and spectral features. The outcome of selection yields a useful hint for further investigation of physiological processes inherent in epileptic signals, since every IMF has its own characteristics related to specific activities of neural/neuronal centres. In addition, the present work indicates the importance of the scales, higher than 4, that are not sufficiently considered or studied in literature [55].

The preliminary clustering, in the present work, can lead to initial understanding of the differences, either in amplitude or frequency content (or eventually both of them), between components of normal, ictal and inter-ictal activities; this can assist practitioners in identifying the related physiological variations.

A hidden additional advantage of the proposed method is the preliminary potential of distinguishing the seizure zone and the opposite inter-ictal hemisphere. Results (not shown) indicate classification accuracy of normal/ictal/inter-ictal (seizure zone)/inter-ictal (opposite hemisphere) up to 85%. This can partially lend a hand for detecting zones of seizure. However, more investigations should be carried out in order to improve this result and examine its applicability.

Although the proposed classification has many advantages, it has been shown that mode mixing and mode intermittency are the major limitations to the use of EMD [35]. Mode mixing indicates that oscillations of different time scales coexist in a given IMF, or that oscillations with the same time scale are assigned to different IMFs, leading to a misunderstanding of the real process. Since EMD has the disadvantage of occasional mode mixing, this might affect slightly the calculation of instantaneous values. The amplitude and frequency ratios between the components of the signal should be taken into account when mode mixing is studied, which is not always easy. Furthermore, solutions proposed in literature to avoid intermittency are either time consuming like the Ensemble Empirical Mode decomposition EEMD or unstable like the use of masking signals [37]. However, according to the obtained results, the achieved accuracy is not severely harmed by the mixing. This might be due to the fact that mixing occurs usually between consecutive IMFs that carry quasi-similar neural processes or activities from the same neural source. Since the solutions of mode mixing are time consuming or unstable, as indicated above, the performance of the suggested method should be carefully studied before application in cases of real-time seizure prediction. Mode mixing can occur in EEG segments related to transition between two different states.

The fact that a part of the calculations is based on missing values is probably considered as a disadvantage. This can be avoided by decomposing all studied signals into a fixed number of IMFs scales. This leads to counterpart IMFs in the same octave, which might make more robust clustering and classification of features. Multivariate Empirical Mode Decomposition can be one of the solutions that might be approached in future works.


The present work studies a robust method that helps classify EEG into normal, ictal and inter-ictal. High accuracy is achieved compared to previous literature. The intuitive characteristics of EMD, the advantages of DQ normalization, the quantification of synchronization level by entropy and the fast easy-to-interpret Random Forest classifier are the main promising elements.

In future work, application of multivariate empirical mode decomposition will be investigated in order to get the same number of IMFs for all studied EEG signals. This might help avoid features with missing values. Furthermore, additional features as variance and other types of entropy will be studied.

The suggested processing has the potential of classifying normal, ictal and inter-ictal EEG. Further directed improvements on the proposed method will allow an approach towards accurate seizures detection and management. More investigation should be conducted to study the applicability of the classification to eventual seizure prediction, especially the investigation of the effect of mode mixing. Targeted enhancements, with the help of neural mapping, might also facilitate seizure prevention prior to onset as well as guidance in neurosurgical interventions.

Change history

  • 09 February 2018

    The article “Classification of Normal, Ictal and Inter-ictal EEG via Direct Quadrature and Random Forest Tree”, written by Enas Abdulhay, Maha Alafeef, Arwa Abdelhay, Areen Al-Bashir was originally published Online First without open access. After publication in volume [37], issue [6], page [843–857] the author decided to opt for Open Choice and to make the article an open access publication. Therefore, the copyright of the article has been changed to © The Author(s) [2018] and the article is forthwith distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits use, duplication, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

  • 09 February 2018

    The article ���Classification of Normal, Ictal and Inter-ictal EEG via Direct Quadrature and Random Forest Tree���, written by Enas Abdulhay, Maha Alafeef, Arwa Abdelhay, Areen Al-Bashir was originally published Online First without open access. After publication in volume [37], issue [6], page [843���857] the author decided to opt for Open Choice and to make the article an open access publication. Therefore, the copyright of the article has been changed to �� The Author(s) [2018] and the article is forthwith distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits use, duplication, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.


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Abdulhay, E., Alafeef, M., Abdelhay, A. et al. Classification of Normal, Ictal and Inter-ictal EEG via Direct Quadrature and Random Forest Tree. J. Med. Biol. Eng. 37, 843–857 (2017).

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  • EEG
  • Forest tree
  • Ictal
  • Direct quadrature
  • Decomposition
  • Entropy
  • Instantaneous