I am trying to implement an algorithm described in this paper:
Decomposition of biospeckle images in temporary spectral bands
Here is an explanation of the algorithm:
We recorded a sequence of
N
successive speckle images with a sampling frequencyfs
. In this way it was possible to observe how a pixel evolves through theN
images. That evolution can be treated as a time series and can be processed in the following way: Each signal corresponding to the evolution of every pixel was used as input to a bank of filters. The intensity values were previously divided by their temporal mean value to minimize local differences in reflectivity or illumination of the object. The maximum frequency that can be adequately analyzed is determined by the sampling theorem and s half of sampling frequencyfs
. The latter is set by the CCD camera, the size of the image, and the frame grabber. The bank of filters is outlined in Fig. 1.In our case, ten 5° order Butterworth filters were used, but this number can be varied according to the required discrimination. The bank was implemented in a computer using MATLAB software. We chose the Butter-worth filter because, in addition to its simplicity, it is maximally flat. Other filters, an infinite impulse response, or a finite impulse response could be used.
By means of this bank of filters, ten corresponding signals of each filter of each temporary pixel evolution were obtained as output. Average energy Eb in each signal was then calculated:
where
pb(n)
is the intensity of the filtered pixel in the nth image for filterb
divided by its mean value andN
is the total number of images. In this way,En
values of energy for each pixel were obtained, each of hem belonging to one of the frequency bands in Fig. 1.With these values it is possible to build ten images of the active object, each one of which shows how much energy of time-varying speckle there is in a certain frequency band. False color assignment to the gray levels in the results would help in discrimination.
and here is my MATLAB code base on that :
for i=1:520
for j=1:368
ts = [];
for k=1:600
ts = [ts D{k}(i,j)]; %%% kth image pixel i,j --- ts is time series
end
ts = double(ts);
temp = mean(ts);
if (temp==0)
for l=1:10
filtImag1{l}(i,j)=0;
end
continue;
end
ts = ts-temp;
ts = ts/temp;
N = 5; % filter order
W = [0.0 0.10;0.10 0.20;0.20 0.30;0.30 0.40;0.40 0.50;0.50 0.60 ;0.60 0.70;0.70 0.80 ;0.80 0.90;0.90 1.0];
[B,A]=butter(N,0.10,'low');
ts_f(1,:) = filter(B,A,ts);
N1 = 5;
for ind = 2:9
Wn = W(ind,:);
[B,A] = butter(N1,Wn);
ts_f(ind,:) = filter(B,A,ts);
end
[B,A]=butter(N,0.90,'high');
ts_f(10,:) = filter(B,A,ts);
for ind=1:10
%Following Paper Suggestion
filtImag1{ind}(i,j) =sum(ts_f(ind,:).^2);
end
end
end
for i=1:10
figure,imshow(filtImag1{i});
colorbar
end
pre_max = max(filtImag1{1}(:));
for i=1:10
new_max = max(filtImag1{i}(:));
if (pre_max<new_max)
pre_max=max(filtImag1{i}(:));
end
end
new_max = pre_max;
pre_min = min(filtImag1{1}(:));
for i=1:10
new_min = min(filtImag1{i}(:));
if (pre_min>new_min)
pre_min = min(filtImag1{i}(:));
end
end
new_min = pre_min;
%normalize
for i=1:10
temp_imag = filtImag1{i}(:,:);
x=isnan(temp_imag);
temp_imag(x)=0;
t_max = max(max(temp_imag));
t_min = min(min(temp_imag));
temp_imag = (double(temp_imag-t_min)).*((double(new_max)-double(new_min))/double(t_max-t_min))+(double(new_min));
%median filter
%temp_imag = medfilt2(temp_imag);
imag_test2{i}(:,:) = temp_imag;
end
for i=1:10
figure,imshow(imag_test2{i});
colorbar
end
for i=1:10
A=imag_test2{i}(:,:);
B=A/max(max(A));
B=histeq(A);
figure,imshow(B);
colorbar
imag_test2{i}(:,:)=B;
end
but I am not getting the same result as paper. has anybody has any idea why? or where I have gone wrong?
EDIT by getting help from @Amro and using his code I endup with the following images: here is my Original Image from 72hrs germinated Lentil (400 images, with 5 frame per second):
here is the results images for 10 different band :