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STUDENT
: CHUA BOON JIN (Q0706456)
SUPERVISOR
: DR RAJENDRA ACHARYA U
PROJECT CODE : JAN2010/BME/0018
Abstract
The aim of this paper is to interpret EEG signal to enable neurologist to diagnose epilepsy
more effectively. EEG data was obtained from Bonn University and Non-linear Analysis
was used for this paper with a total of 8 entropies estimators used. These entropies
estimators are Bi-Spectral Entropy 1 and 2, Approximate Entropy, Wen Entropy, Sample
Entropy, Shannon Spectral Entropy, Renyis Entropy and Kalmogorov-Sinai Entropy. By
using ANOVA test, a low p-value (probability value) of < 0.0001 was achieved for all of
our entropies estimators used except Shannon Spectral Entropy. For classification, 4
entropies estimators namely Approximate Entropy, Renyis Entropy, Bi-Spectral Entropy 1
and Sample Entropy were used. The highest classification rate of 94.44% for GMM
classifier was achieved. To further improve the accuracy rate of the probability of epilepsy
better, a new parameter known as Index was introduced. By using the same 4 entropies
estimators used for classification, a low p-value of < 0.0001 was achieved. The same as the
7 entropies estimators used earlier. This further proves that entropies estimators are able to
predict normal, epilepsy and pre-ictal effectively to enhance the probability of a correct
diagnosis for patients.
Acknowledgement
I would like to thank Dr Rajendra Acharya U for his time and effort to guide me in this
project. Without his help and guidance, this project would not be a success. I would also
like to thank all anonymous reviewers for their comments and suggestions and those who
have helped me in one way or another. Once again, thank you all for all your kind
assistance.
Table of Contents
ABSTRACT .....................................................................................................................................................I
ACKNOWLEDGEMENT ...................................................................................................................................I
TABLE OF CONTENTS ....................................................................................................................................II
LIST OF FIGURES ......................................................................................................................................... IV
LIST OF TABLES ........................................................................................................................................... IV
LIST OF SYMBOLS ....................................................................................................................................... IV
CHAPTER 1 ................................................................................................................................................... 1
INTRODUCTION ................................................................................................................................................... 1
CHAPTER 2 ................................................................................................................................................... 5
DATA ................................................................................................................................................................ 5
ENTROPY ESTIMATORS ......................................................................................................................................... 6
Bi-Spectral Entropy 1 and 2 ........................................................................................................................ 6
Approximate Entropy ................................................................................................................................. 8
Wen Entropy ............................................................................................................................................... 8
Sample Entropy .......................................................................................................................................... 8
Shannon Spectral Entropy .......................................................................................................................... 9
Renyis Entropy ........................................................................................................................................... 9
Kalmogorov-Sinai Entropy ....................................................................................................................... 10
CLASSIFIERS ...................................................................................................................................................... 10
Fuzzy Sugeno Classifier ............................................................................................................................. 10
Gaussian Mixture Model .......................................................................................................................... 11
CHAPTER 3 ................................................................................................................................................. 13
RESULTS........................................................................................................................................................... 13
DISCUSSION...................................................................................................................................................... 22
CHAPTER 4 ................................................................................................................................................. 24
SUMMARY ....................................................................................................................................................... 24
CONCLUSION .................................................................................................................................................... 24
FUTURE WORKS ................................................................................................................................................ 24
CHAPTER 5 ................................................................................................................................................. 25
REFLECTION ...................................................................................................................................................... 25
REFERENCES ............................................................................................................................................... 27
APPENDIX A ENTROPY VALUES ................................................................................................................ 30
ENTROPY VALUES FOR NORMAL SIGNAL ................................................................................................................ 30
ENTROPY VALUES FOR EPILEPSY SIGNAL................................................................................................................. 34
ENTROPY VALUES FOR PRE-ICTAL SIGNAL............................................................................................................... 36
APPENDIX B ENTROPY CODES .................................................................................................................. 41
BI-SPECTRAL ENTROPY CODES ............................................................................................................................. 41
APPROXIMATE ENTROPY CODES........................................................................................................................... 42
ii
iii
List of Figures
-
List of Tables
-
List of Symbols
Summation
Heaviside function
Pie
Set Membership
iv
Chapter 1
Introduction
The brain is a large and highly complex organ. The four major components of the brain
consist of the cerebrum, cerebellum, diencephalon and brain stem. Cerebrum is the largest
portion of the brain and its functions include sensory, motor and association areas where
they inter-relate sensory and motor areas in the interrelationships of personality traits,
memory and intellectual processes. Cerebellum is the second largest and is in-charge of
balance and coordination of muscle. Diencephalon and brain stem are for relaying sensory
impulses and regulate body functions. The brain also contains billion of nerve cells or
neurons. Nerve cells or neurons communicate in the brain by sending electrical impulses
with each other. The movement of electrical signals excites or inhibits between nerve cells
trigger by chemical reaction, produces thought, feeling, movement and memories. When
the electrical signals excite too far out of the balance between excitation and inhabitation,
misfiring occurs and this usually causes seizures. Depending on where the signal originates
from, the type of seizures varies. If it is from the motor region, a motor seizure; if from a
sensory region, a sensory perception; if the seizures spread to all region of the brain, then a
tonic-clonic seizure results, with body jerking and stiffness. These misfiring electrical
signals cause a brief interruption in the brain activities in which the suffered is unaware of.
A seizure may just happen suddenly and usually last from a few seconds to a few minutes.
Some factors that provoke seizures include stress, flashing light, alcohol and alcohol
withdrawal. A single seizure is not epilepsy. It is only when more seizures occur along a
period of time, then it can be considered as epilepsy.
Epilepsy is a general term used to describe a neurological brain disorder. It is not
contagious and is not a disease. Most of the occurred epilepsy remained unknown, only a
handful of it was known. Some known causes of epilepsy includes stroke, lack of oxygen to
the brain, high fever and brain tumour. Epilepsy can affect anyone, anywhere and anytime
regardless of how old you are.
A successful diagnostic test includes detail history of episodes information such as
blood test, Magnetic Resonance Imaging (MRI) scan and Electroencephalogram (EEG)
test. Blood test is done to look for any infectious or chemical cause of seizures. Blood test
is also important if antiepileptic drugs are to be used. MRI is used to scan the brain to check
if there are any underlying structural causes such as blood clot or tumour. MRI is more
detailed than CT or X-ray as it produces more slice images of the brain. EEG is used to
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measure electrical signals produced by the brain. Electrodes are placed in different position
on the scalp with adhesive paste. The electrodes are wired to an amplifier and to a
recording device with monitor. The electrical signals released by neurons in the brain are
captured by electrodes, amplify and convert it into waveforms, which are shown on the
monitor. These patterns of waveforms are used to determine if the patients are suffering
from epilepsy or any other brain associated disorders. Experience electroencephalographers
will be able to recognize these patterns. During recording, the patients may be asked to do
certain things such as looking at flashing light, breathe heavily or to blink the eyes.
Abnormal EEG signal known as spikes, enable electroencephalographers to mark
the tendency for seizures. Such spikes are also known as inter-ictal spikes because they
happen in between seizures. However, there are some important factors to know about
EEG test. Firstly, an EEG test cannot be used to diagnose epilepsy. It can only be used as a
tool to support the patients medical history, which has consistent seizures attack.
Abnormal spikes in EEG signal does not necessary mean a person is not normal especially
when they did not suffer from any seizure in the past. Secondly, a negative EEG test should
not discourage the clinician from treating especially when the patients has a history of
seizures attack. Therefore, EEG test is helpful in getting information to support the
diagnosis of epilepsy and to classify the types of EEG signal.
For engineers and researchers understanding these waveforms requires knowledge
of signal processing skills in relation to physiological events. Over the years, many
experiments were done using various methods to analyse EEG waveform. These include
Fast Fourier Transform (FFT), Autoregression (AR) method, Autoregressive-moving
average (ARMA) method, Time Varying Autoregression (TVAR) method, Fast Wavelet
Transform (FWT), Principal Component Analysis (PCA), Fast Independent Component
Analysis (FastICA) and Entropies Estimators.
There are a lot of FFT algorithms involved in mathematics from simple complex
number arithmetic to group theory and number theory. The most common FFT algorithm is
based on Cooley-Tukey algorithm [Cooley and Tukey, 1965]. Cooley-Tukey algorithm
breaks down Discrete Fourier Transform (DFT) into smaller bits of DFT such that it can be
combined arbitrarily with any known FFT algorithm for DFT.
FWT is another algorithm used to interpret EEG waveforms. As compared to
Fourier transform, FWT looks for space distribution of singularities instead of overall
regularity of signals [Geva and Kerem, 1998]. FWT can also accommodate wandering
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signals unlike Fourier transform, which captures stationary signal. FWT is suitable for EEG
signal interpretation as it is non-stationary in nature and its frequency content is time
variant.
TVAR is a new method of breaking down time series and provides clear
representations on EEG time frequency structure. TVAR model was developed such that
the breakdown of time series signal leads to a more significant data analysis method in the
context of state-space models [Andrew D. Krystal et al. 1999]. The data analysis arising in
state-space representation is based on instantaneous, time-evolving eigen structure analysis
of matrices.
AR method is another way to interpret EEG signal. Based on time series, AR is able
to show the centre frequency, associated power and number of oscillatory components.
Autocovariance and Autocorrelation are the 2 methods to calculate AR [R.Ghafar et al.
2008]. Autocorrelation is the more consistent of the 2 methods in displaying the frequency.
ARMA model consists of a number of finite sets of parameters (parametric model).
Dependent on its random disturbance and past values, approximate calculation of its time
series at a time can be estimated. ARMA is able to capture the required information within
the time-varying parameters of the input signal [Vangelis Sakkalis et al. 2008]. Akaike
information criterion (AIC) can be used to determine the model order for ARMA [Vangelis
Sakkalis et al 2008, Shinn-Yih Tseng et al 1993].
FastICA is a statistical signal processing technique to describe the EEG signal. It is
one of the most popular ICA algorithms. The properties of this algorithm include fast and
global convergence for certain contrasts and mixing conditions and is capable to cope well
even when noise is present. The reason to use FastICA is because the algorithm is able to
identify non-gaussian distribution directly.
PCA is used mainly for feature extraction or dimension reduction in EEG analysis.
It can express relevant information in the EEG signal by converting correlated variable into
a new uncorrelated variable by uses fewer dimensions [Sheng-Fu Liang et al. 2010].
Entropies estimators are part of non-linear analysis of time varying signals. This
entropy refers to information theory described by [C.E.Shannon, 1948] in his article A
Mathematical Theory of Communication and is unlike the entropy in thermodynamics.
Confusion between these two entropies is common. Entropy is an uncertainty value usually
associated with a random variable. It is like information contain in a message. This value is
what we obtained by running it with several of entropies algorithm.
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CHAPTER 2
Classifier
EEG Signal
Entropies
Estimators
ANOVA
Test
Results
Index
Entropy Estimators
8 entropies were used for this assignment. These are Bi-Spectral Entropy 1 and 2,
Approximate Entropy, Wen Entropy, Sample Entropy, Shannon Spectral Entropy, Renyis
Entropy and Kalmogorov-Sinai Entropy. More details will be discussed in this section.
Bi-Spectral Entropy 1 and 2
Bi-Spectral is a higher order statistic analysis tool use for studying non-linear quadratic
function. It has a triangular region known as the non-redundant region of computation
(Figure 1) [Chua et al. 2010].
Non-redundant
Region
0.5
f2
0.5
f1
iBi j
Bi j
f 2m
jBi j
Bi j
Where i and j are the frequency bin index in the non-redundant region
Normalized bispectral entropy (BE 1):
P1 pi log p1
where
pi
B f1 , f 2
B f , f
P2 p n log p n
where
pn
B f1 , f 2
B f , f
1m1
N
m
m
APEN
m
,
r
,
N
log
C
r
log
C
r
i
i
1
i
1 i
N
1
N
where C im r
N m 1
1
r xi x j
N m 1 j 1
For this project, m is set to 5 and r is set to0.2 the standard deviation of original data
sequence.
Wen Entropy
Wen entropy is available in Matlab as wentropy under wavelet toolbox. The syntax for
wentropy is:
E wentropy X , T
where X is the input data, T is a string containing the type of entropy.
largely independent of data length. [Physio Toolkit, Richman and Randall 2000]. SampEn
can be calculated by using this equation:
SampEn (k , r , N ) ln
A(k )
for k 0,1,...,m 1 with B(0) N , the length of the input
B(k 1)
f log
p
f
f
High entropy data have broad flat probability distribution while low entropy data have
narrow peaked probability distribution [Kannathal et al. 2006].
Renyis Entropy
Renyis entropy is given by:
1
REN
log
p
1
k where
In this paper, we used a 2 to determined the REN for normal and epileptic EEG data.
This is a special case called Renyis quadratic entropy. Renyis quadratic entropy is given
by:
REN
2
log
p
The difference between REN and SEN is that REN data is weighted towards frequencies
in the lower frequency band. [Kannathal et al. 2006].
Kalmogorov-Sinai Entropy
Kalmogorov-Sinai entropy measures the time taken for 2 points in the time series to move
apart. Kalmogorov Sinai entropy is given as:
expressed in bits/sec.
N
m
m
2N
r
,N
1C
m
m
C
r
,
N
m
m
i
j
K
lim
lim
is the
N
N
1
r
0
m
1
j
1
m
m
where
C
r
,N
m
1
m
1
j
which input variables affect the output. Parameter identification identifies the parameters in
both premises and consequences [Yaochu Jin et al. 1995]. Consider a fuzzy system with K
input and fuzzy implication R.
R if x1 is A1 , ... , x k is Ak then y g x1 ,..., x k
where
x1 x k is the premise variables
10
A1 Ak is the fuzzy subspace along a linear membership function used for reasoning
y y y
y
yy
i
where
x;
2 2
d
T
exp x 1 x
2
1
2
Where
and
is the determinant
A k-component GMM is defined as:
f k x j x; j with
k
j 1
j 1
1 for j 0 : j 1..... k
where
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11
j P j | xi / n
i 1
j P j | xi xi / n j
n
i 1
j P j | xi xi i xi i / n j
n
i 1
12
CHAPTER 3
Results
8 entropy values were obtained after running them through their respective Matlab program
from the 3 classes of EEG data. Entropy values of these 8 entropies are shown in Appendix
A. These 8 entropy values were used to obtain their mean, standard deviation, P
(probability) value and Group Mean with 95% Confidence Interval value by using ANOVA
(Analysis Of Variance) test. Table 1 shows the results for ANOVA test.
Entropies
Bi Spectral
Entropy 1
Bi Spectral
Entropy 2
Kalmogorov-Sinai
Entropy
Sample Entropy
Shannon Spectral
Entropy
Renyis Entropy
Approximate
Entropy
Wentropy
Normal
Epilepsy
Pre-Ictal
P - Value
0.565707.634E-02
0.483250.155
0.471325.833E-02
< 0.0001
0.773773.163E-02
0.731844.555E-02
0.678113.926E-02
< 0.0001
7.68840E031.408E-02
1.33240.122
3.36197E027.547E-02
0.926470.139
2.16623E024.632E-02
1.01750.163
N.A.
-16.339 0.653
-19.535 1.02
-16.378 0.935
< 0.0001
2.2512 5.578E-02
1.9325 0.215
1.8785 0.256
< 0.0001
-5.17516E+07
5.255E+07
-2.75498E+09
2.540E+09
-1.41293E+08
7.067E+08
< 0.0001
13
< 0.0001
< 0.0001
14
15
From the results we can see that all the p-value is very small at < 0.0001. This means that
the probabilities of obtaining very different or more different results as compared to the
results shown above are very small. Assuming all the data collected was correct.
4 sets of data namely Renyis, Bi-Spec 1, SampEn and ApEn were fed into 2 classifier
Fuzzy and GMM. Before the data can be fed into the classifier, these data must be sort into
training and testing categories. 100 data from each class were selected to be split into
training and testing. 70 data from each class were used for training while 30 were used for
testing. The 70 training data were mixed into rows by rows of normal, epilepsy and preictal while the testing data were arranged by normal data at the top followed by epilepsy
data and lastly pre-ictal data. These data were known as training1 and testing 1. 2 more sets
of training and testing data were created. These were achieved by swapping the 30 testing1
data to training1 and the first 30 of training1 data to testing1. These data were arranged
according to their respective arrangement as mentioned above. These data were named as
testing2 and training2. The 30 testing2 data were once again swap with the next 30 of
training2 and arranged according to their arrangement and these data were named as
testing3 and training3. The results for GMM are shown on Table 2.
EEG Data
Pre-Ictal
Normal
30
Epilepsy
28
Pre-Ictal
27
Sensitivity =
90.91%
Specificity =
100%
Sensitivity =
96.55%
Specificity =
98.33%
Sensitivity =
96.43%
Specificity =
95.16%
PPV = 100%
NPV = 95%
PPV = 93.33%
NPV = 98.33%
PPV = 90%
NPV = 98.33%
Pre-Ictal
Normal
27
Epilepsy
29
16
PPV = 90%
NPV = 100%
PPV = 96.67%
NPV = 98.33%
Pre-Ictal
29
Sensitivity =
100%
Specificity =
95.24%
Sensitivity =
96.66%
Specificity =
98.33%
Sensitivity =
87.88%
Specificity =
98.24%
PPV = 96.67%
NPV = 93.33%
EEG Data
Pre-Ictal
Normal
29
Epilepsy
29
Pre-Ictal
26
Sensitivity =
93.55%
Specificity =
98.31%
Sensitivity =
90.63%
Specificity =
98.23%
Sensitivity =
96.30%
Specificity =
93.65%
PPV = 96.67%
NPV = 96.67%
PPV = 96.67%
NPV = 95.00%
PPV = 86.67%
NPV = 98.33%
17
EEG Data
Normal
28
Epilepsy
21
Pre-Ictal
24
Sensitivity =
75.68%
Specificity =
96.23%
Sensitivity =
87.50%
Specificity =
86.36%
Sensitivity =
82.76%
Specificity =
90.16%
PPV =
NPV =
PPV =
NPV =
PPV =
NPV =
93.33%
85.00%
70.00%
95.00%
80.00%
91.67%
PPV =
NPV =
PPV =
NPV =
PPV =
NPV =
86.67%
90.00%
76.67%
93.33%
90.00%
93.33%
EEG Data
Normal
26
Epilepsy
23
Pre-Ictal
27
Sensitivity =
81.25%
Specificity =
93.10%
Sensitivity =
85.19%
Specificity =
88.89%
Sensitivity =
87.10%
Specificity =
94.92%
EEG Data
Normal
29
Epilepsy
24
Pre-Ictal
24
Sensitivity =
74.36%
Specificity =
98.04%
Sensitivity =
100.00%
Specificity =
90.91%
Sensitivity =
88.89%
Specificity =
90.48%
18
PPV =
NPV =
PPV =
NPV =
PPV =
NPV =
96.67%
83.33%
80.00%
100.00%
80.00%
95.00%
From the results, the highest classification rate achieved was 85.56%. Sensitivity range
from 74.36% to 100% and this proves that Fuzzy is not as sensitive when it comes to
predicting the TP of normal, epilepsy or pre-ictal signals as compared to GMM. Specificity
for Fuzzy range from 86.36% to 98.04% and this again shows there is quite a number of
FP generated by Fuzzy and this can hinder the accuracy of predicting these EEG signals.
PPV for Fuzzy range from 70% to 96.67% and NPV range from 83.33% to 100%. Table 4
shows the comparison between GMM and Fuzzy.
Classification
Sensitivity
Specificity
PPV
NPV
90.91%
100%
100%
95%
96.55%
98.33%
93.33%
98.33%
Pre-Ictal
96.43%
95.16%
90%
98.33%
Normal
75.68%
96.23%
93.33%
85.00%
87.50%
86.36%
70.00%
95.00%
Pre-Ictal
82.76%
90.16%
80.00%
91.67%
Normal
100%
95.24%
90%
100%
96.66%
98.33%
96.67%
98.33%
Pre-Ictal
87.88%
98.24%
96.67%
93.33%
Normal
81.25%
93.10%
86.67%
90.00%
85.19%
88.89%
76.67%
93.33%
Pre-Ictal
87.10%
94.92%
90.00%
93.33%
Normal
93.55%
98.31%
96.67%
96.67%
90.63%
98.23%
96.67%
95%
Pre-Ictal
96.30%
93.65%
86.67%
98.33%
Normal
74.36%
98.04%
96.67%
83.33%
100.00%
90.91%
80.00%
100.00%
88.89%
90.48%
80.00%
95.00%
Normal
GMM
Fuzzy
GMM
Fuzzy
GMM
Fuzzy
Test1
Test1
Test2
Test2
Test3
Test3
Epilepsy
Epilepsy
Epilepsy
Epilepsy
Epilepsy
Epilepsy
Pre-Ictal
94.44%
81.11%
94.44%
84.44%
93.33%
85.56%
19
Table 5 shows the result for Index using ANOVA test. The probability value is < 0.0001,
which shows index can be used for correctly predicting the outcome.
Entropies
Index
Normal
0.601352.047E-02
Epilepsy
0.707793.170E-02
Pre-Ictal
0.663095.876E-02
Probability Value
< 0.0001
20
For easy access of deducing the result, a GUI was created to incorporate all data needed to
deduce the final results. These results will tell us whether the EEG signal is normal,
epilepsy or pre-ictal. Graphical details of GUI are shown below.
21
Method
Classifier
Accuracy
This Paper
90%
Paper by
Kannathal et al.
92.26%
Paper by U. R.
Acharya et al.
94.44%
22
Kannathal N. et al. (2006) demonstrated similar reading in his work. Using Spectral
Entropy, Renyis Entropy, Kalmogorov-Sinai Entropy and Approximate Entropy with
Adaptive Neuro-Fuzzy Inference System (ANFIS) classifier, Kannathal N. et al. (2006)
reported higher value for normal state and a lower value for epileptic state. This shows that
normal state is more chaotic than epileptic state. Classification rate for normal state shows
93.02% while epileptic state shows 91.49% with an average of 92.26% accuracy.
In another paper by U.R. Acharya et al. (2009), Approximate Entropy, Correlation
Dimension, Fractal Dimension, Hurst Exponent and Largest Lyapunov Exponent together
with GMM and Support Vector Machine (SVM) classifier were used for feature extraction
and classification. U.R. Acharya et al. (2009) achieved a p (probability) -value of < 0.0001
for all entropies used. GMM classifier reported an average of 95% accuracy and SVM
reported an average of 93.88% accuracy with a total average of 94.44%.
H. Adeli et al. (2006) uses a wavelet-chaos methodology to analyse EEG data.
Discrete wavelet transform is used to decompose into delta, theta, alpha, beta and gamma
sub-bands. Correlation Dimension and Largest Lyapunov Exponent are used to quantify
EEG signal. Result shows higher entropy value for normal EEG signal as compared to
epileptic EEG signal. This means higher chaoticity for normal state.
For this paper, Approximate Entropy, Bi-Spectral Entropy 1, Sample Entropy and
Renyis Entropy used to for classification. Classification rate achieved for Fuzzy was
85.56% and 94.44% for GMM. Average accuracy for both classifiers was 90%. This is
lower as compared to other papers but this can be further improved by having more training
data. Entropy values for normal state show higher value than epileptic state with p-value of
< 0.0001 from ANOVA test. This proves normal state signal are more chaotic.
The above studies have shown that entropies estimator can be used as a tool to
extract EEG features. To further improve the accuracy of the differentiating the EEG
signal, we propose a new parameter known as Index. Index uses part of the entropies
estimators to form a formula and evaluate the EEG signal. Classification from the index
reported 94.44%. ANOVA test shows the value for normal, epilepsy and pre-ictal are well
space out for group mean of 95% greater confidence interval. This means the value
obtained from index can be greatly differentiate between normal, epilepsy and pre-ictal
EEG signal and enhance its accuracy.
23
CHAPTER 4
Summary
Electroencephalogram or EEG as most of us call it is actually electrical signal captured by
neurons firing in the brain. Sometimes these neurons misfire and thus cause epilepsy. To
fully understand these neurons firing pattern and accurately interpret epilepsy, non-linear
analysis such as entropies estimators were used. 8 entropies estimators namely Bi-Spectral
Entropy 1 and 2, Approximate Entropy, Sample Entropy, Spectral Shannon Entropy,
Kalmogorov-Sinai Entropy, Wen Entropy and Renyis Entropy were used for features
extraction. ANOVA test on these 8 entropies reported a p-value of < 0.0001%. 4 entropies
namely Approximate Entropy, Bi-Spectral Entropy 1, Renyis Entropy and Sample Entropy
were used for classification and reported results of 94.44%. These same 4 entropies were
later used for index. Index is a new parameter developed to predict EEG more accurately.
ANOVA test on index yield positive result with p-value of < 0.0001 and group mean with
95% confidence interval evenly space out between normal, epilepsy and pre-ictal signal.
This proves entropies estimators can be used as a tool to interpret epilepsy successfully.
Conclusion
EEG signal generated from the EEG machine tells us about the neurological behaviour of
the person at that time. To interpret these signals, various forms of research had been
undertaken in the past. Research using non-linear analysis has shown promising results.
From the results shown above, non-linear algorithm such as entropies estimators have
shown that it was possible to be used as a feature extraction tool. Results were comparable
with others paper using similar entropies estimators. Classification results also show similar
characteristics too. The use of index is a new method proposed in this paper that is
definitely a new way to interpret EEG signal with accuracy and precision. With this project,
hopefully a new method to assist neurologist in interpreting EEG comes a step closer.
Future Works
For future works, more training data are required to train the classifier to obtain 100%
classification rate. More variation of epilepsy EEG data is also required such as low risk
epilepsy, high-risk epilepsy and very high-risk epilepsy to fully understand the variation of
EEG signal.
BME499 ENG499 MTD499 ICT499 MTH499 CAPSTONE PROJECT REPORT
24
Chapter 5
Reflection
The time has finally come... its a long way but certainly a bright future ahead. Before I
step onto the steps of graduation, together with all my peers and mates, there is one last
item left to tackle and this item is my capstone project.
It has come a long way since the beginning of the year when I started my project. I
can still remember when the time has come to choose a project, I was apprehensive at first
if I should attempt it together with my other modules or to attempt it after I finished all my
modules so that I could concentrate on it 100%. In the end, the urge to graduate faster got
the better of me.
The time was December 2009 when I was required to choose a project via the
student portal. Instruction given was given out to all students taking capstone that the
selection of project is based on first come first choose basis. The fastest you log in, the
more projects to choose from. I log in around 1205 hrs and to my amazement, a lot of the
project was snap up. There were people more anxious than I was. In the end, the project I
select was Entropies for Detection of Epilepsy in EEG. This project requires the user to
have knowledge of Matlab.
I started this project with little knowledge of Matlab; only those basic skills which I
learnt in class. Nevertheless, I decided to give it a go. During the first project meeting with
my project supervisor, Dr Raj, he gave me a firm assurance and that helps greatly. First up,
is the project proposal, after which are the interim report and lastly the final project report.
In between these reports, lie the main dish, Matlab, entropies algorithm and more Matlab.
Initially, while doing my project proposal, I had to read up on a couple of journal
papers to understand what entropy is all about. There is also classifier, which I had never
heard of until then. As the project wore on, more entropy was added to increase its accuracy
and predictability.
Throughout the project, other than recalling what I learnt previously, I also pick up
other skills in Matlab that I never thought I could actually used Matlab to do. One such
example was GUI. Matlab GUI was similar to Visual Basic with its drag and drop interface.
The only difference is the programming codes. After some trial and error, I managed to get
my GUI running. It was such a relief and at the same time felt with a sense of satisfaction.
BME499 ENG499 MTD499 ICT499 MTH499 CAPSTONE PROJECT REPORT
25
But the job does not end here, to make it to the finishing line; we still need to finish this
final project report and the presentation that comes after.
Keep going and preserve till the end. Rewards will come after that.
Only those who attempt the absurd will achieve the impossible. M. C. ESCHER
26
References
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A.E. White, M.J. Burin, T.A. Carter, T.S. Hahm, J.A. Krommes, R.J. Maqueda, S.J.
Zweben (2006), Bispectral analysis of low to high confinement mode transitions in
the National Spherical Torus Experiment, American Institute of Physics, doi:
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A.P. Dempster, N.M. Laird, D.B. Rubin (1977), Maximum likelihood from
incomplete data via the EM algorithm, Journal of the Royal Statistical Society
Series B(Methodological), Vol 39, No. 1. pp 1-38
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[4]
Andrew D. Krystal, Rqquel Prado, Mike West (1999), New methods of time series
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Physio Toolkit
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http://www. physionet.org/physiotools/ApEn/
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R. Ghafar, A. Hussain, S.A. Samad, N.M. Tahir (2008) Comparison of FFT and AR
techniques for scalp EEG analysis, IFMBE proceedings, Vol. 21 pp 158-161
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Tomohiro Takagi, Michio Sugeno (1985), Fuzzy identification of systems and its
applications to modeling and control, IEEE Transactions on systems, man, and
cybernetics, Vol. SMC-15, pp 116-132
[21]
U.R. Acharya, K.C. Chua, T.C. Lim, Dorithy, J.S. Suri (2009), Automatic
identification of epileptic EEG signals using nonlinear parameters, Journal of
Mechanics in Medicine and Biology, Vol. 9, No. 4 pp. 539-553
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Yaochu Jin, Jingping Jiang, Jing Zhu (1995), Neural network based fuzzy
identification and its application to modeling and control of complex systems, IEEE
Transactions on systems, man and cybernetics, Vol. 25, no. 6
29
Bi-Spec 1
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Kalmogorov
SampEn
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Shannon
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Renyi's
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AppEn
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Kalmogorov
5.21552E-09
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Shannon
1358160.409
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Renyi's
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Wentropy
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Kalmogorov
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%direct method
41
42
43
44
=
=
=
=
=
n*(n-1)/2;
match(1:M); %first element of match to M to A
[N;A(1:(M-1))];
A./B; %A right array divide of B
-log(p); %to calculate entropy value
45
46
47
Appendix C - GUI
GUI Main Screen Codes
function varargout = EEG(varargin)
% EEG M-file for EEG.fig
%
EEG, by itself, creates a new EEG or raises the existing
%
singleton*.
%
%
H = EEG returns the handle to a new EEG or the handle to
%
the existing singleton*.
%
%
EEG('CALLBACK',hObject,eventData,handles,...) calls the local
%
function named CALLBACK in EEG.M with the given input arguments.
%
%
EEG('Property','Value',...) creates a new EEG or raises the
%
existing singleton*. Starting from the left, property value pairs
are
%
applied to the GUI before EEG_OpeningFcn gets called. An
%
unrecognized property name or invalid value makes property
application
%
stop. All inputs are passed to EEG_OpeningFcn via varargin.
%
%
*See GUI Options on GUIDE's Tools menu. Choose "GUI allows only
one
%
instance to run (singleton)".
%
% See also: GUIDE, GUIDATA, GUIHANDLES
% Edit the above text to modify the response to help EEG
% Last Modified by GUIDE v2.5 02-Oct-2010 15:32:55
% Begin initialization code - DO NOT EDIT
gui_Singleton = 1;
gui_State = struct('gui_Name',
mfilename, ...
'gui_Singleton', gui_Singleton, ...
'gui_OpeningFcn', @EEG_OpeningFcn, ...
'gui_OutputFcn', @EEG_OutputFcn, ...
'gui_LayoutFcn', [] , ...
'gui_Callback',
[]);
if nargin && ischar(varargin{1})
gui_State.gui_Callback = str2func(varargin{1});
end
if nargout
[varargout{1:nargout}] = gui_mainfcn(gui_State, varargin{:});
else
gui_mainfcn(gui_State, varargin{:});
end
% End initialization code - DO NOT EDIT
48
% --- Outputs from this function are returned to the command line.
function varargout = EEG_OutputFcn(hObject, eventdata, handles)
% varargout cell array for returning output args (see VARARGOUT);
% hObject
handle to figure
% eventdata reserved - to be defined in a future version of MATLAB
% handles
structure with handles and user data (see GUIDATA)
% Get default command line output from handles structure
varargout{1} = handles.output;
49
a = str2num(get(handles.app,'string'));
b = str2num(get(handles.bi1,'string'));
c = str2num(get(handles.ren,'string'));
d = str2num(get(handles.sam,'string'));
e = (c+a+b+d)/(c-a-b-d);
set(handles.text12,'string',e);
if ((e >= 0.5934) && (e <= 0.6093))
set(handles.edit_result,'string','Normal');
elseif ((e >= 0.6999) && (e <= 0.7157))
set(handles.edit_result,'string','Epilepsy');
elseif ((e >= 0.6552) && (e <= 0.6720))
set(handles.edit_result,'string','Background');
else
set(handles.edit_result,'string','Unknown');
end
guidata(hObject, handles);
% --- Executes on button press in Browse.
function Browse_Callback(hObject, eventdata, handles)
% hObject
handle to Browse (see GCBO)
% eventdata reserved - to be defined in a future version of MATLAB
% handles
structure with handles and user data (see GUIDATA)
w = cd();
[filename, pathname] = uigetfile('*.txt', 'Open an EEG data');
cd(pathname);
data = load(filename);
set(handles.Screen,'String',data);
cd(w);
plot(handles.graph, data);
guidata(hObject, handles);
50
guidata(hObject, handles);
51
52
end
53
% hObject
% eventdata
% handles
54
%
str2double(get(hObject,'String')) returns contents of
edit_result as a double
55
56
gui_State = struct('gui_Name',
mfilename, ...
'gui_Singleton', gui_Singleton, ...
'gui_OpeningFcn', @EEG_Output_OpeningFcn, ...
'gui_OutputFcn', @EEG_Output_OutputFcn, ...
'gui_LayoutFcn', [] , ...
'gui_Callback',
[]);
if nargin && ischar(varargin{1})
gui_State.gui_Callback = str2func(varargin{1});
end
if nargout
[varargout{1:nargout}] = gui_mainfcn(gui_State, varargin{:});
else
gui_mainfcn(gui_State, varargin{:});
end
% End initialization code - DO NOT EDIT
% --- Executes just before EEG_Output is made visible.
function EEG_Output_OpeningFcn(hObject, eventdata, handles, varargin)
% This function has no output args, see OutputFcn.
% hObject
handle to figure
% eventdata reserved - to be defined in a future version of MATLAB
% handles
structure with handles and user data (see GUIDATA)
% varargin
command line arguments to EEG_Output (see VARARGIN)
% Choose default command line output for EEG_Output
handles.output = hObject;
% Update handles structure
guidata(hObject, handles);
% UIWAIT makes EEG_Output wait for user response (see UIRESUME)
% uiwait(handles.figure1);
% --- Outputs from this function are returned to the command line.
function varargout = EEG_Output_OutputFcn(hObject, eventdata, handles)
% varargout cell array for returning output args (see VARARGOUT);
% hObject
handle to figure
% eventdata reserved - to be defined in a future version of MATLAB
% handles
structure with handles and user data (see GUIDATA)
% Get default command line output from handles structure
varargout{1} = handles.output;
% --- Executes on selection change in EEG_data.
function EEG_data_Callback(hObject, eventdata, handles)
% hObject
handle to EEG_data (see GCBO)
% eventdata reserved - to be defined in a future version of MATLAB
% handles
structure with handles and user data (see GUIDATA)
set(varargin);
% Hints: contents = get(hObject,'String') returns EEG_data contents as
cell array
%
contents{get(hObject,'Value')} returns selected item from
EEG_data
% --- Executes during object creation, after setting all properties.
function EEG_data_CreateFcn(hObject, eventdata, handles)
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% hObject
% eventdata
% handles
called
58
Appendix D - Classifier
Fuzzy Classifier Codes
clear all;
clc;
load normalisedtraining3woapp
load normalisedtesting3woapp
load class
%features
p1 = training(:,1);
p2 = training(:,2);
p3 = training(:,3);
p4 = training(:,4);
%p5 = training(:,5);
%p6 = training(:,6);
%p7 = training(:,7);
%p8 = training(:,8);
%classes
t1 = class(:,1);
t2 = class(:,2);
t3 = class(:,3);
p = [p1';p2';p3';p4'];
t = [t1';t2';t3'];
%features
test1 = testing(:,1);
test2 = testing(:,2);
test3 = testing(:,3);
test4 = testing(:,4);
%test5 = testing(:,5);
%test6 = testing(:,6);
%test7 = testing(:,7);
%test8 = testing(:,8);
test = [test1';test2';test3';test4'];
ptest=test';
fismat = genfis2(p',t',0.5,[0 0 0 0 0 0 0; 1 1 1 1 1 1 1]); %Generate
Fuzzy Inference System structure from data using subtractive clustering
y=evalfis(ptest,fismat); %Perform fuzzy inference calculations
outres=y';
yj=outres';
for i=1:length(yj)
a=yj(i,:);
maxi=max(a); %largest elements in array
for j=1:3
if yj(i,j)==maxi
yj(i,j)=1;
else
yj(i,j)=0;
end
end
end
yj
xlswrite('Fuzzywoapp.xls', yj, 'Fuzzy3', 'A1'); %to create excel file
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% mixture model 1
% mixture model 2
% mixture model 3
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% Convert to 1 of N encoding
target = [ test_label==1 test_label==2
test_label==3];
%No. of outputs
fh1 = conffig(test_probs, target);
function plotmat(matrix, textcolour, gridcolour, fontsize)
%PLOTMAT Display a matrix.
%
%
Description
%
PLOTMAT(MATRIX, TEXTCOLOUR, GRIDCOLOUR, FONTSIZE) displays the matrix
%
MATRIX on the current figure. The TEXTCOLOUR and GRIDCOLOUR
%
arguments control the colours of the numbers and grid labels
%
respectively and should follow the usual Matlab specification. The
%
parameter FONTSIZE should be an integer.
%
%
See also
%
CONFFIG, DEMMLP2
%
%
[m,n]=size(matrix);
for rowCnt=1:m,
for colCnt=1:n,
numberString=num2str(matrix(rowCnt,colCnt));
text(colCnt-.5,m-rowCnt+.5,numberString, ...
'HorizontalAlignment','center', ...
'Color', textcolour, ...
'FontWeight','bold', ...
'FontSize', fontsize);
end;
end;
set(gca,'Box','on', ...
'Visible','on', ...
'xLim',[0 n], ...
'xGrid','on', ...
'xTickLabel',[], ...
'xTick',0:n, ...
'yGrid','on', ...
'yLim',[0 m], ...
'yTickLabel',[], ...
'yTick',0:m, ...
'DataAspectRatio',[1, 1, 1], ...
'GridLineStyle',':', ...
'LineWidth',3, ...
'XColor',gridcolour, ...
'YColor',gridcolour);
function [centres, options, post, errlog] = kmeans(centres, data,
options)
%KMEANS Trains a k means cluster model.
%
%
Description
%
CENTRES = KMEANS(CENTRES, DATA, OPTIONS) uses the batch K-means
%
algorithm to set the centres of a cluster model. The matrix DATA
%
represents the data which is being clustered, with each row
%
corresponding to a vector. The sum of squares error function is used.
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%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
%
62
perm = perm(1:ncentres);
% Assign first ncentres (permuted) data points as centres
centres = data(perm, :);
end
% Matrix to make unit vectors easy to construct
id = eye(ncentres);
% Main loop of algorithm
for n = 1:niters
% Save old centres to check for termination
old_centres = centres;
% Calculate posteriors based on existing centres
d2 = dist2(data, centres);
% Assign each point to nearest centre
[minvals, index] = min(d2', [], 1);
post = id(index,:);
num_points = sum(post, 1);
% Adjust the centres based on new posteriors
for j = 1:ncentres
if (num_points(j) > 0)
centres(j,:) = sum(data(find(post(:,j)),:), 1)/num_points(j);
end
end
% Error value is total squared distance from cluster centres
e = sum(minvals);
if store
errlog(n) = e;
end
if options(1) > 0
fprintf(1, 'Cycle %4d Error %11.6f\n', n, e);
end
if n > 1
% Test for termination
if max(max(abs(centres - old_centres))) < options(2) & ...
abs(old_e - e) < options(3)
options(8) = e;
return;
end
end
old_e = e;
end
% If we get here, then we haven't terminated in the given number of
% iterations.
options(8) = e;
if (options(1) >= 0)
disp(maxitmess);
end
function prob = gmmprob(mix, x)
%GMMPROB Computes the data probability for a Gaussian mixture model.
%
%
Description
%
This function computes the unconditional data density P(X) for a
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%
%
%
%
%
%
%
Gaussian mixture model. The data structure MIX defines the mixture
model, while the matrix X contains the data vectors. Each row of X
represents a single vector.
See also
GMM, GMMPOST, GMMACTIV
64
65
66
%
%
%
%
%
%
%
%
The optional return value OPTIONS contains the final error value
(i.e. data log likelihood) in OPTIONS(8).
See also
GMM, GMMINIT
67
if display > 0
fprintf(1, 'Cycle %4d Error %11.6f\n', n, e);
end
if test
if (n > 1 & abs(e - eold) < options(3))
options(8) = e;
return;
else
eold = e;
end
end
end
% Adjust the new estimates for the parameters
new_pr = sum(post, 1);
new_c = post' * x;
% Now move new estimates to old parameter vectors
mix.priors = new_pr ./ ndata;
mix.centres = new_c ./ (new_pr' * ones(1, mix.nin));
switch mix.covar_type
case 'spherical'
n2 = dist2(x, mix.centres);
for j = 1:mix.ncentres
v(j) = (post(:,j)'*n2(:,j));
end
mix.covars = ((v./new_pr))./mix.nin;
if check_covars
% Ensure that no covariance is too small
for j = 1:mix.ncentres
if mix.covars(j) < MIN_COVAR
mix.covars(j) = init_covars(j);
end
end
end
case 'diag'
for j = 1:mix.ncentres
diffs = x - (ones(ndata, 1) * mix.centres(j,:));
mix.covars(j,:) = sum((diffs.*diffs).*(post(:,j)*ones(1, ...
mix.nin)), 1)./new_pr(j);
end
if check_covars
% Ensure that no covariance is too small
for j = 1:mix.ncentres
if min(mix.covars(j,:)) < MIN_COVAR
mix.covars(j,:) = init_covars(j,:);
end
end
end
case 'full'
for j = 1:mix.ncentres
diffs = x - (ones(ndata, 1) * mix.centres(j,:));
diffs = diffs.*(sqrt(post(:,j))*ones(1, mix.nin));
mix.covars(:,:,j) = (diffs'*diffs)/new_pr(j);
end
if check_covars
% Ensure that no covariance is too small
for j = 1:mix.ncentres
if min(svd(mix.covars(:,:,j))) < MIN_COVAR
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mix.covars(:,:,j) = init_covars(:,:,j);
end
end
end
case 'ppca'
for j = 1:mix.ncentres
diffs = x - (ones(ndata, 1) * mix.centres(j,:));
diffs = diffs.*(sqrt(post(:,j))*ones(1, mix.nin));
[tempcovars, tempU, templambda] = ...
ppca((diffs'*diffs)/new_pr(j), mix.ppca_dim);
if length(templambda) ~= mix.ppca_dim
error('Unable to extract enough components');
else
mix.covars(j) = tempcovars;
mix.U(:, :, j) = tempU;
mix.lambda(j, :) = templambda;
end
end
if check_covars
if mix.covars(j) < MIN_COVAR
mix.covars(j) = init_covars(j);
end
end
otherwise
error(['Unknown covariance type ', mix.covar_type]);
end
end
options(8) = -sum(log(gmmprob(mix, x)));
if (display >= 0)
disp(maxitmess);
end
function a = gmmactiv(mix, x)
%GMMACTIV Computes the activations of a Gaussian mixture model.
%
%
Description
%
This function computes the activations A (i.e. the probability
%
P(X|J) of the data conditioned on each component density) for a
%
Gaussian mixture model. For the PPCA model, each activation is the
%
conditional probability of X given that it is generated by the
%
component subspace. The data structure MIX defines the mixture model,
%
while the matrix X contains the data vectors. Each row of X
%
represents a single vector.
%
%
See also
%
GMM, GMMPOST, GMMPROB
%
%
% Preallocate matrix
switch mix.covar_type
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case 'spherical'
% Calculate squared norm matrix, of dimension (ndata, ncentres)
n2 = dist2(x, mix.centres);
% Calculate width factors
wi2 = ones(ndata, 1) * (2 .* mix.covars);
normal = (pi .* wi2) .^ (mix.nin/2);
% Now compute the activations
a = exp(-(n2./wi2))./ normal;
case 'diag'
normal = (2*pi)^(mix.nin/2);
s = prod(sqrt(mix.covars), 2);
for j = 1:mix.ncentres
diffs = x - (ones(ndata, 1) * mix.centres(j, :));
a(:, j) = exp(-0.5*sum((diffs.*diffs)./(ones(ndata, 1) * ...
mix.covars(j, :)), 2)) ./ (normal*s(j));
end
case 'full'
normal = (2*pi)^(mix.nin/2);
for j = 1:mix.ncentres
diffs = x - (ones(ndata, 1) * mix.centres(j, :));
% Use Cholesky decomposition of covariance matrix to speed
computation
c = chol(mix.covars(:, :, j));
temp = diffs/c;
a(:, j) = exp(-0.5*sum(temp.*temp, 2))./(normal*prod(diag(c)));
end
case 'ppca'
log_normal = mix.nin*log(2*pi);
d2 = zeros(ndata, mix.ncentres);
logZ = zeros(1, mix.ncentres);
for i = 1:mix.ncentres
k = 1 - mix.covars(i)./mix.lambda(i, :);
logZ(i) = log_normal + mix.nin*log(mix.covars(i)) - ...
sum(log(1 - k));
diffs = x - ones(ndata, 1)*mix.centres(i, :);
proj = diffs*mix.U(:, :, i);
d2(:,i) = (sum(diffs.*diffs, 2) - ...
sum((proj.*(ones(ndata, 1)*k)).*proj, 2)) / ...
mix.covars(i);
end
a = exp(-0.5*(d2 + ones(ndata, 1)*logZ));
otherwise
error(['Unknown covariance type ', mix.covar_type]);
end
function mix = gmm(dim, ncentres, covar_type, ppca_dim)
%GMM
Creates a Gaussian mixture model with specified architecture.
%
%
Description
%
MIX = GMM(DIM, NCENTRES, COVARTYPE) takes the dimension of the space
%
DIM, the number of centres in the mixture model and the type of the
%
mixture model, and returns a data structure MIX. The mixture model
%
type defines the covariance structure of each component Gaussian:
%
'spherical' = single variance parameter for each component: stored
as a vector
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%
'diag' = diagonal matrix for each component: stored as rows of a
matrix
%
'full' = full matrix for each component: stored as 3d array
%
'ppca' = probabilistic PCA: stored as principal components (in a 3d
array
%
and associated variances and off-subspace noise
%
MIX = GMM(DIM, NCENTRES, COVARTYPE, PPCA_DIM) also sets the
%
dimension of the PPCA sub-spaces: the default value is one.
%
%
The priors are initialised to equal values summing to one, and the
%
covariances are all the identity matrix (or equivalent). The centres
%
are initialised randomly from a zero mean unit variance Gaussian.
%
This makes use of the MATLAB function RANDN and so the seed for the
%
random weight initialisation can be set using RANDN('STATE', S) where
%
S is the state value.
%
%
The fields in MIX are
%
%
type = 'gmm'
%
nin = the dimension of the space
%
ncentres = number of mixture components
%
covartype = string for type of variance model
%
priors = mixing coefficients
%
centres = means of Gaussians: stored as rows of a matrix
%
covars = covariances of Gaussians
%
The additional fields for mixtures of PPCA are
%
U = principal component subspaces
%
lambda = in-space covariances: stored as rows of a matrix
%
The off-subspace noise is stored in COVARS.
%
%
See also
%
GMMPAK, GMMUNPAK, GMMSAMP, GMMINIT, GMMEM, GMMACTIV, GMMPOST,
%
GMMPROB
%
%
if ncentres < 1
error('Number of centres must be greater than zero')
end
mix.type = 'gmm';
mix.nin = dim;
mix.ncentres = ncentres;
vartypes = {'spherical', 'diag', 'full', 'ppca'};
if sum(strcmp(covar_type, vartypes)) == 0
error('Undefined covariance type')
else
mix.covar_type = covar_type;
end
% Make default dimension of PPCA subspaces one.
if strcmp(covar_type, 'ppca')
if nargin < 4
ppca_dim = 1;
end
if ppca_dim > dim
error('Dimension of PPCA subspaces must be less than data.')
end
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mix.ppca_dim = ppca_dim;
end
% Initialise priors to be equal and summing to one
mix.priors = ones(1,mix.ncentres) ./ mix.ncentres;
% Initialise centres
mix.centres = randn(mix.ncentres, mix.nin);
% Initialise all the variances to unity
switch mix.covar_type
case 'spherical'
mix.covars = ones(1, mix.ncentres);
mix.nwts = mix.ncentres + mix.ncentres*mix.nin + mix.ncentres;
case 'diag'
% Store diagonals of covariance matrices as rows in a matrix
mix.covars = ones(mix.ncentres, mix.nin);
mix.nwts = mix.ncentres + mix.ncentres*mix.nin + ...
mix.ncentres*mix.nin;
case 'full'
% Store covariance matrices in a row vector of matrices
mix.covars = repmat(eye(mix.nin), [1 1 mix.ncentres]);
mix.nwts = mix.ncentres + mix.ncentres*mix.nin + ...
mix.ncentres*mix.nin*mix.nin;
case 'ppca'
% This is the off-subspace noise: make it smaller than
% lambdas
mix.covars = 0.1*ones(1, mix.ncentres);
% Also set aside storage for principal components and
% associated variances
init_space = eye(mix.nin);
init_space = init_space(:, 1:mix.ppca_dim);
init_space(mix.ppca_dim+1:mix.nin, :) = ...
ones(mix.nin - mix.ppca_dim, mix.ppca_dim);
mix.U = repmat(init_space , [1 1 mix.ncentres]);
mix.lambda = ones(mix.ncentres, mix.ppca_dim);
% Take account of additional parameters
mix.nwts = mix.ncentres + mix.ncentres*mix.nin + ...
mix.ncentres + mix.ncentres*mix.ppca_dim + ...
mix.ncentres*mix.nin*mix.ppca_dim;
otherwise
error(['Unknown covariance type ', mix.covar_type]);
end
function n2 = dist2(x, c)
%DIST2 Calculates squared distance between two sets of points.
%
%
Description
%
D = DIST2(X, C) takes two matrices of vectors and calculates the
%
squared Euclidean distance between them. Both matrices must be of
%
the same column dimension. If X has M rows and N columns, and C has
%
L rows and N columns, then the result has M rows and L columns. The
%
I, Jth entry is the squared distance from the Ith row of X to the
%
Jth row of C.
%
%
See also
%
GMMACTIV, KMEANS, RBFFWD
%
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errstring = ['Model type ''', s, ''' does not match expected type
''',...
type, ''''];
return
end
end
% If inputs are present, check that they have correct dimension
if nargin > 2
if ~isfield(model, 'nin')
errstring = 'Data structure does not contain nin field';
return
end
data_nin = size(inputs, 2);
if model.nin ~= data_nin
errstring = ['Dimension of inputs ', num2str(data_nin), ...
' does not match number of model inputs ', num2str(model.nin)];
return
end
end
% If outputs are present, check that they have correct dimension
if nargin > 3
if ~isfield(model, 'nout')
errstring = 'Data structure does not conatin nout field';
return
end
data_nout = size(outputs, 2);
if model.nout ~= data_nout
errstring = ['Dimension of outputs ', num2str(data_nout), ...
' does not match number of model outputs ', num2str(model.nout)];
return
end
% Also check that number of data points in inputs and outputs is the same
num_in = size(inputs, 1);
num_out = size(outputs, 1);
if num_in ~= num_out
errstring = ['Number of input patterns ', num2str(num_in), ...
' does not match number of output patterns ', num2str(num_out)];
return
end
end
function [C,rate]=confmat(Y,T)
%CONFMAT Compute a confusion matrix.
%
%
Description
%
[C, RATE] = CONFMAT(Y, T) computes the confusion matrix C and
%
classification performance RATE for the predictions mat{y} compared
%
with the targets T. The data is assumed to be in a 1-of-N encoding,
%
unless there is just one column, when it is assumed to be a 2 class
%
problem with a 0-1 encoding. Each row of Y and T corresponds to a
%
single example.
%
%
In the confusion matrix, the rows represent the true classes and the
%
columns the predicted classes. The vector RATE has two entries: the
%
percentage of correct classifications and the total number of correct
%
classifications.
%
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%
%
%
See also
CONFFIG, DEMTRAIN
[n c]=size(Y);
[n2 c2]=size(T);
if n~=n2 | c~=c2
error('Outputs and targets are different sizes')
end
if c > 1
% Find the winning class assuming 1-of-N encoding
[maximum Yclass] = max(Y', [], 1);
TL=[1:c]*T';
else
% Assume two classes with 0-1 encoding
c = 2;
class2 = find(T > 0.5);
TL = ones(n, 1);
TL(class2) = 2;
class2 = find(Y > 0.5);
Yclass = ones(n, 1);
Yclass(class2) = 2;
end
% Compute
correct = (Yclass==TL);
total=sum(sum(correct));
rate=[total*100/n total];
C=zeros(c,c);
for i=1:c
for j=1:c
C(i,j) = sum((Yclass==j).*(TL==i));
end
end
function fh=conffig(y, t)
%CONFFIG Display a confusion matrix.
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Description
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CONFFIG(Y, T) displays the confusion matrix and classification
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performance for the predictions mat{y} compared with the targets T.
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The data is assumed to be in a 1-of-N encoding, unless there is just
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one column, when it is assumed to be a 2 class problem with a 0-1
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encoding. Each row of Y and T corresponds to a single example.
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In the confusion matrix, the rows represent the true classes and the
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columns the predicted classes.
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FH = CONFFIG(Y, T) also returns the figure handle FH which can be
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used, for instance, to delete the figure when it is no longer needed.
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See also
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CONFMAT, DEMTRAIN
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