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(Genetic Algorithms: Form and Function)
 
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1.      Genetic algorithms (GAs): basic form
 
1.      Genetic algorithms (GAs): basic form
  
A generic GA (aka evolutionary algorithm [EA]) assumes a discrete search space H and a function
+
A generic GA (also know as an evolutionary algorithm [EA]) assumes a discrete search space H and a function
                                          \[f:H\to\mathbb{R}\],                         
+
                                          \[f:H\to\mathbb{R}\],                         
where H is a subsetof the Euclidean space \[\mathbb{R}\].
+
where H is a subsetof the Euclidean space\[\mathbb{R}\].
 
The general problem is to find
 
The general problem is to find
                                          \[\arg\underset{X\in H}{\mathop{\min }}\,f\],
+
                                          \[\arg\underset{X\in H}{\mathop{\min }}\,f\],
 
where X is avector of the decision variables and f is the objective function.
 
where X is avector of the decision variables and f is the objective function.
With GAs it is customary to distinguish genotype–the encoded representation of the variables–from phenotype–the set of variablesthemselves. The vector X isrepresented by a string (or chromosome) s of length l madeup of symbols drawn from an alphabet Ausing the mapping
+
 
                                          \[c:{{A}^{l}}\toH\].
+
With GAs it is customary to distinguish genotype–the encoded representation of the variables–from phenotype–the set of variablesthemselves. The vector X is represented by a string (or chromosome) s of length l madeup of symbols drawn from an alphabet Ausing the mapping
 +
                                          \[c:{{A}^{l}}\toH\].
 
The mapping c is not necessarily surjective. The range of c determine the subset of Al  available for exploration by a GA.
 
The mapping c is not necessarily surjective. The range of c determine the subset of Al  available for exploration by a GA.
 
The range of c, Ξ  
 
The range of c, Ξ  
                                          \[\Xi\subseteq {{A}^{l}}\]
+
                                          \[\Xi\subseteq {{A}^{l}}\]
isneeded to account for the fact that some strings in the image Al under c may represent invalid solutions to the original problem.
+
is needed to account for the fact that some strings in the image Al under c may represent invalid solutions to the original problem.
 +
 
 +
The string length l depends on the dimensions of both H and A, with the elements of the string corresponding to genes and the valuesto alleles. This statement of genes and alleles is often referred to as genotype-phenotype mapping.
  
The string length l depends on thedimensions of both H and A, with the elements of the string corresponding to genes and the valuesto alleles. This statement of genes and alleles is often referred to as genotype-phenotype mapping.
 
 
Given the statements above, the optimization becomes:
 
Given the statements above, the optimization becomes:
                                \[\arg\underset{S\in L}{\mathop{\min g}}\,\],
+
 
 +
                                  \[\arg\underset{S\in L}{\mathop{\min g}}\,\],
 
given the function  
 
given the function  
                                                                                                \[g(s)=f(c(s))\].
+
 
 +
                                  \[g(s)=f(c(s))\].
 +
 
 
Finally, with GAs it is helpful if c is a bijection. The important property of bijections as they applyto GAs is that bijections have an inverse, i.e., there is a unique vector x for every string and a unique stringfor each x.  
 
Finally, with GAs it is helpful if c is a bijection. The important property of bijections as they applyto GAs is that bijections have an inverse, i.e., there is a unique vector x for every string and a unique stringfor each x.  
1.      Genetic algorithms and their operators
 
The following statementsabout the operators of Gas is adopted from Coello et al.  (Coello, 2002).
 
·        Let H be a nonempty set (the individual orsearch space), \[{{\left\{ {{u}^{i}} \right\}}_{i\in \mathbb{N}}}\] asequence in \[{{\mathbb{Z}}^{+}}\] (the parent populations),
 
·        \[{{\left\{ {{u}^{'(i)}} \right\}}_{i\in\mathbb{N}}}\] a sequence in \[{{\mathbb{Z}}^{+}}\](the offspring populationsizes)
 
·        \[\phi :H\to \mathbb{R}\] a fitness function, \[\iota:\cup _{i=1}^{\infty }{{({{H}^{u}})}^{(i)}}\to \] {true, false} (thetermination criteria)
 
·        \[\chi \in \]{true, false}, r a sequence \[\left\{ {{r}^{(i)}} \right\}\] of recombinationoperators τ(i) : \[X_{r}^{(i)}\toT(\Omega _{r}^{(i)}
 
·        m asequence of {m(i)} ofmutation operators in mi
 
·        \[X_{m}^{(i)}\to T(\Omega _{m}^{(i)},T\left({{H}^{{{u}^{(i)}}}},{{H}^{u{{'}^{(i)}}}} \right))\], s a sequence of {si}selection operators s(i)
 
·        \[X_{s}^{(i)}\times T(H,\mathbb{R})\to T(\Omega_{s}^{(i)},T(({{H}^{u{{'}^{(i)+\chi {{\mu }^{(i)}}}}}}),{{H}^{{{\mu}^{(i+1)}}}}))\], \[\Theta _{r}^{(i)}\in X_{r}^{(i)}\] (the recombinationparameters)
 
·        \[\Theta _{m}^{(i)}\in X_{m}^{(i)}\] (themutation parameters)
 
·        \[\Theta _{s}^{(i)}\in X_{s}^{(i)}\] (theselection parameters)
 
  
+
 
 +
2.      Genetic algorithms and their operators
 +
The following statements about the operators of GAs are adopted from Coello et al.(2002).
 +
 
 +
·        Let H be a nonempty set (the individual orsearch space)
 +
·      \[{{\left\{{{u}^{i}} \right\}}_{i\in \mathbb{N}}}\] a sequence in \[{{\mathbb{Z}}^{+}}\](the parent populations),
 +
·      \[{{\left\{ {{u}^{'(i)}} \right\}}_{i\in\mathbb{N}}}\] a sequence in \[{{\mathbb{Z}}^{+}}\](the offspring population sizes)
 +
·        \[\phi :H\to \mathbb{R}\] a fitness function
 +
·        \[\iota:\cup _{i=1}^{\infty }{{({{H}^{u}})}^{(i)}}\to \] {true, false} (the termination criteria)
 +
·      \[\chi \in \]{true, false}, r a sequence \[\left\{ {{r}^{(i)}} \right\}\] of recombination operators τ(i) : \[X_{r}^{(i)}\toT(\Omega _{r}^{(i)}
 +
·        m a sequence of {m(i)} of mutation operators in mi
 +
·        \[X_{m}^{(i)}\to T(\Omega _{m}^{(i)},T\left({{H}^{{{u}^{(i)}}}},{{H}^{u{{'}^{(i)}}}} \right))\], s a sequence of {si} selection operators s(i)
 +
·        \[X_{s}^{(i)}\times T(H,\mathbb{R})\to T(\Omega_{s}^{(i)},T(({{H}^{u{{'}^{(i)+\chi {{\mu }^{(i)}}}}}}),{{H}^{{{\mu}^{(i+1)}}}}))\], \[\Theta _{r}^{(i)}\in X_{r}^{(i)}\] (the recombination parameters)
 +
·        \[\Theta _{m}^{(i)}\in X_{m}^{(i)}\] (the mutation parameters)
 +
·        \[\Theta _{s}^{(i)}\in X_{s}^{(i)}\] (the selection parameters)
 +
 
 +
 
 +
 
 
Coello et al. define the collection μ (thenumber of individuals) via Hμ.The population transforms are denoted by\[T:{{H}^{\mu }}\to {{H}^{\mu }}\],where\[\mu \in \mathbb{N}\]. However, some GA methods generate populationswhose size is not equal to their predecessors’. In a more general framework \[T:{{H}^{\mu}}\to {{H}^{{{\mu }'}}}\]can accommodate populations that contain the same ordifferent individuals. This mapping has the ability to represent all populationsizes, evolutionary operators, and parameters as sequences.
 
Coello et al. define the collection μ (thenumber of individuals) via Hμ.The population transforms are denoted by\[T:{{H}^{\mu }}\to {{H}^{\mu }}\],where\[\mu \in \mathbb{N}\]. However, some GA methods generate populationswhose size is not equal to their predecessors’. In a more general framework \[T:{{H}^{\mu}}\to {{H}^{{{\mu }'}}}\]can accommodate populations that contain the same ordifferent individuals. This mapping has the ability to represent all populationsizes, evolutionary operators, and parameters as sequences.

Revision as of 14:17, 14 August 2012

Bold textGenetic Algorithms


1. Genetic algorithms (GAs): basic form

A generic GA (also know as an evolutionary algorithm [EA]) assumes a discrete search space H and a function

                                          \[f:H\to\mathbb{R}\],                         

where H is a subsetof the Euclidean space\[\mathbb{R}\]. The general problem is to find

                                          \[\arg\underset{X\in H}{\mathop{\min }}\,f\],

where X is avector of the decision variables and f is the objective function.

With GAs it is customary to distinguish genotype–the encoded representation of the variables–from phenotype–the set of variablesthemselves. The vector X is represented by a string (or chromosome) s of length l madeup of symbols drawn from an alphabet Ausing the mapping

                                          \[c:{{A}^{l}}\toH\].

The mapping c is not necessarily surjective. The range of c determine the subset of Al available for exploration by a GA. The range of c, Ξ

                                          \[\Xi\subseteq {{A}^{l}}\]

is needed to account for the fact that some strings in the image Al under c may represent invalid solutions to the original problem.

The string length l depends on the dimensions of both H and A, with the elements of the string corresponding to genes and the valuesto alleles. This statement of genes and alleles is often referred to as genotype-phenotype mapping.

Given the statements above, the optimization becomes:

                                 \[\arg\underset{S\in L}{\mathop{\min g}}\,\],

given the function

                                  \[g(s)=f(c(s))\].

Finally, with GAs it is helpful if c is a bijection. The important property of bijections as they applyto GAs is that bijections have an inverse, i.e., there is a unique vector x for every string and a unique stringfor each x.


2. Genetic algorithms and their operators The following statements about the operators of GAs are adopted from Coello et al.(2002).

· Let H be a nonempty set (the individual orsearch space) · \[{{\left\{{{u}^{i}} \right\}}_{i\in \mathbb{N}}}\] a sequence in \[{{\mathbb{Z}}^{+}}\](the parent populations), · \[{{\left\{ {{u}^{'(i)}} \right\}}_{i\in\mathbb{N}}}\] a sequence in \[{{\mathbb{Z}}^{+}}\](the offspring population sizes) · \[\phi :H\to \mathbb{R}\] a fitness function · \[\iota:\cup _{i=1}^{\infty }{{({{H}^{u}})}^{(i)}}\to \] {true, false} (the termination criteria) · \[\chi \in \]{true, false}, r a sequence \[\left\{ {{r}^{(i)}} \right\}\] of recombination operators τ(i) : \[X_{r}^{(i)}\toT(\Omega _{r}^{(i)} · m a sequence of {m(i)} of mutation operators in mi · \[X_{m}^{(i)}\to T(\Omega _{m}^{(i)},T\left({{H}^{{{u}^{(i)}}}},{{H}^{u{{'}^{(i)}}}} \right))\], s a sequence of {si} selection operators s(i) · \[X_{s}^{(i)}\times T(H,\mathbb{R})\to T(\Omega_{s}^{(i)},T(({{H}^{u{{'}^{(i)+\chi {{\mu }^{(i)}}}}}}),{{H}^{{{\mu}^{(i+1)}}}}))\], \[\Theta _{r}^{(i)}\in X_{r}^{(i)}\] (the recombination parameters) · \[\Theta _{m}^{(i)}\in X_{m}^{(i)}\] (the mutation parameters) · \[\Theta _{s}^{(i)}\in X_{s}^{(i)}\] (the selection parameters)


Coello et al. define the collection μ (thenumber of individuals) via Hμ.The population transforms are denoted by\[T:{{H}^{\mu }}\to {{H}^{\mu }}\],where\[\mu \in \mathbb{N}\]. However, some GA methods generate populationswhose size is not equal to their predecessors’. In a more general framework \[T:{{H}^{\mu}}\to {{H}^{{{\mu }'}}}\]can accommodate populations that contain the same ordifferent individuals. This mapping has the ability to represent all populationsizes, evolutionary operators, and parameters as sequences.

How to Cite This Entry:
Genetic Algorithms. Encyclopedia of Mathematics. URL: http://encyclopediaofmath.org/index.php?title=Genetic_Algorithms&oldid=27537