Bacterial Foraging Optimization Algorithm
Bacterial Foraging Optimization Algorithm
ENGINEERING
PROBLEM
Submitted By:
-
5/20/2019
Table of Contents
Bacterial foraging optimization ...................................................................................................... 3
Abstract ................................................................................................................................................... 3
Introduction ............................................................................................................................................ 3
Literature Review: ................................................................................................................................... 3
Different Types of Derivative Free Optimization ........................................................................ 4
Bacterial Foraging Optimization ............................................................................................................. 4
algorithm ................................................................................................................................................. 6
Flowchart ................................................................................................................................................ 8
Code: ....................................................................................................................................................... 9
Results; .................................................................................................................................................. 13
Comparison: .......................................................................................................................................... 15
Advantages:........................................................................................................................................... 15
Conclusion ............................................................................................................................................. 15
References ............................................................................................................................................ 16
2
Bacterial foraging optimization
Abstract
Introduction
Optimization problems defined by functions for which derivatives are unavailable or
available at a prohibitive cost are appearing more and more frequently in
computational science and engineering. Increasing complexity in mathematical
modelling, higher sophistication of scientific computing, and abundance of legacy
codes are some of the reasons why derivative-free optimization is currently an area
of great demand.
In many physical applications, the true models or functions being optimized are
extremely expensive to evaluate but, based e.g. on simplified physics or mesh
coarsening, there are often surrogate models available, less accurate but cheaper to
evaluate. In these circumstances, one would expect to design an optimization
framework capable of extracting as much information as possible from the surrogate
model while parsimoniously using the fine, true model to accurately guide the course
of the optimization process
Literature Review:
Many researchers study the biological evolution and animal behavior, thereby they
put forward many bionic algorithms based on these. Those algorithms include
Genetic Algorithm(GA), Particle Swarm Optimizer(PSO), Ant Colony Optimization
(ACO), Glowworm Swarm Optimization(GSO) and Bee Colony Algorithm(BCA), and
so on. All of them have been developed and used to solve complex optimization
problems.
BFO has has been successfully applied to a variety of problems, such as electrical
engineering and control [2], artificial neural network training [3, 4], pattern
recognition[5], PID controller design[6], portfolio optimization [7] etc. However, as
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other intelligent algorithm, BFO algorithm also could trapped in local minima and its
convergence speed is slow. For improving the BFO’s searching performance, some
mutation algorithms base on BFO were presented, most of them belong to
parameters modification or hybrid algorithms.
In the first case, for example, S. Dasgupta et al. [8] analysis the effect of the adaptive
chemotaxis step size on the convergence and stability of the algorithm. Shao Y. et
al. [9] proposed a cooperative bacterial foraging algorithm base on adaptive
chemotaxis step size. And recently, Tan L, J. et al. [10] present a adaptive bacterial
foraging algorithm with nonlinearly decreasing modulation. In the other case, Kim et
al. proposed a BFOA-Genetic algorithm hybridization for better performance [11].
After that, the other researchers proposed BFOA based on PSO (BSO [12],
BFPSO[13]), BFOA based on Differential Evolution(DE)[14], and BFOA-Estimation of
Distribution Algorithms [15], Bacterial Foraging-Tabu Algorithms [16], BFA Based on
Quantum-behaved Particle Swarm Optimization (OQ-BFA) [17] etc. But, as well as
the literatures[8–10], the previous works in adaptive mechanism focus on the
adaptive chemotaxis step size, while few works pay attention to the elimination-
dispersal probability. In this project, we using an adaptive elimination-dispersal
probability and add
2. Simulated Analysis
4. Swarm Optimization
6. Bacterial Foraging
Chemotaxis
The movement of E. coli bacteria in the human intestine in search of nutrient-rich
location away from noxious environment is accomplished with the help of the
4
locomotory organelles known as flagella by chemotactic movement in either of the
ways, that is, swimming (in the same direction as the previous step) or tumbling (in
an absolutely different direction from the previous one).
Swarming
This group behavior is seen in several motile species of bacteria, where the cells,
when stimulated by a high level of succinate, release an attractant aspertate. This
helps them propagate collectively as concentric patterns of swarms with high
bacterial density while moving up in the nutrient gradient.
Reproduction
The least healthy bacteria constituting half of the bacterial population are eventually
eliminated while each of the healthier bacteria asexually split into two, which are then
placed in the same location. Hence, ultimately the population remains constant.
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algorithm
6
7
Flowchart
8
Code:
clear all;
close all;
clc;
tic
%diary prav;
% Bacteria Foraging Optimization %
for k=1:Np
for i=1:D
x(k,i)=Pmin(i)+rand*(Pmax(i)-Pmin(i));
end
end
%x
% x=(rand(Np,D)-0.5)*60 % x lies in [-30 30]
J=zeros(Np,1);
for k=1:Np
temp1=0;
temp5=0;
for i=1:D
9
temp1=temp1+x(k,i);
temp5=temp5+a(i)+b(i)*x(k,i)+c(i)*x(k,i)*x(k,i)+abs(ee(i)*sin(ff(i)*(Pmin(i)-x(k,i))));
% J(k)=sum(100*(x(k,i+1)-x(k,i)^2)^2+(x(k,i)-1)^2); % initial fitness calculation
end
temp2=Pd-temp1;
temp3=0;
if(temp2>0)
temp3=200.0*temp2;
end
J(k)=temp5+temp3;
end
J;
Jlast=J;
for l=1:Ne
for k=1:Nr
Jchem=J;
for j=1:Nc
% Chemotaxis Loop %
for i=1:Np
del=(rand(1,D)-0.5)*2;
x(i,:)=x(i,:)+(C/sqrt(del*del'))*del;
temp1=0;
temp5=0;
for d=1:D
if(x(i,d)<Pmin(d))
x(i,d)=Pmin(d);
end
if(x(i,d)>Pmax(d))
x(i,d)=Pmax(d);
end
temp1=temp1+x(i,d);
temp5=temp5+a(d)+b(d)*x(i,d)+c(d)*x(i,d)*x(i,d)+abs(ee(d)*sin(ff(d)*(Pmin(d)-
x(i,d))));
%J(i)=sum(100*(x(i,d+1)-x(i,d)^2)^2+(x(i,d)-1)^2);
end
temp2=Pd-temp1;
temp3=0;
if(temp2>0)
10
temp3=200.0*temp2;
end
J(i)=temp5+temp3;
for m=1:Ns
if J(i)<Jlast(i)
Jlast(i)=J(i);
x(i,:)=x(i,:)+C*(del/sqrt(del*del'));
temp1=0;
temp5=0;
for d=1:D
if(x(i,d)<Pmin(d))
x(i,d)=Pmin(d);
end
if(x(i,d)>Pmax(d))
x(i,d)=Pmax(d);
end
temp1=temp1+x(i,d);
temp5=temp5+a(d)+b(d)*x(i,d)+c(d)*x(i,d)*x(i,d)+abs(ee(d)*sin(ff(d)*(Pmin(d)-
x(i,d))));
% J(i)=sum(100*(x(i,d+1)-x(i,d)^2)^2+(x(i,d)-1)^2);
end
temp2=Pd-temp1;
temp3=0;
if(temp2>0)
temp3=200.0*temp2;
end
J(i)=temp5+temp3;
else
del=(rand(1,D)-0.5)*2;
x(i,:)=x(i,:)+C*(del/sqrt(del*del'));
temp1=0;
temp5=0;
for d=1:D
if(x(i,d)<Pmin(d))
x(i,d)=Pmin(d);
end
if(x(i,d)>Pmax(d))
x(i,d)=Pmax(d);
end
temp1=temp1+x(i,d);
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temp5=temp5+a(d)+b(d)*x(i,d)+c(d)*x(i,d)*x(i,d)+abs(ee(d)*sin(ff(d)*(Pmin(d)-
x(i,d))));
% J(i)=sum(100*(x(i,d+1)-x(i,d)^2)^2+(x(i,d)-1)^2);
end
temp2=Pd-temp1;
temp3=0;
if(temp2>0)
temp3=200.0*temp2;
end
J(i)=temp5+temp3;
end
end
end
Jchem=[Jchem J];
end % End of Chemotaxis %
for i=1:Np
Jhealth(i)=sum(Jchem(i,:)); % sum of cost function of all chemotactic loops
for a given k & l
end
[Jhealth1,I]=sort(Jhealth,'ascend');
x=[x(I(1:Np/2),:);x(I(1:Np/2),:)];
J=[J(I(1:Np/2),:);J(I(1:Np/2),:)];
xmin=x(I(1),:);
end
Jmin(l)=min(J);
% random elimination dispersion
for i=1:Np
r=rand;
if r>=Ped
x(i,:)=(rand(1,D)-0.5);
temp1=0;
temp5=0;
for d=1:D
if(x(i,d)<Pmin(d))
x(i,d)=Pmin(d);
end
if(x(i,d)>Pmax(d))
x(i,d)=Pmax(d);
end
12
temp1=temp1+x(i,d);
temp5=temp5+a(d)+b(d)*x(i,d)+c(d)*x(i,d)*x(i,d)+abs(ee(d)*sin(ff(d)*(Pmin(d)-
x(i,d))));
% J(i)=sum(100*(x(i,d+1)-x(i,d)^2)^2+(x(i,d)-1)^2);
end
temp2=Pd-temp1;
temp3=0;
if(temp2>0)
temp3=200.0*temp2;
end
J(i)=temp5+temp3;
end
end
l
Jmin
end
Jmin
plot(Jmin);
xmin
Pg= sum(xmin)
toc
Results;
Non-Convex:
13
Convex:
14
Comparison:
Technique Cost
BFO 8230.3
ACO 8232
GA 8234.07
PSO 8569.2
Advantages:
Conclusion:
15
Bacterial foraging optimization is one of the best optimization techniques for economic dispatch.
The results obtained through our research show us that BFO gives minimum cost for our dispatch.
Bacterial foraging technique has the advantage of having less computational time, less
computational time, global convergence and more probability of convergence.
References
https://www.researchgate.net/publication/226084136_Bacterial_Foraging_Optimizati
on_Algorithm_Theoretical_Foundations_Analysis_and_Applications
https://ieeexplore.ieee.org/document/6153240/references#references
https://www.hindawi.com/journals/acisc/2012/897127/
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