This project's canonical repositories is hosted on Gothel Software.
This genetic algorithm follows the natural process of meiosis, see our meiosis compilation (pdf).
Also available is the ancient German documentation from 1994.
This project is currently under review, see bugzilla Genetic Algorithm Solver:
This document requires a rewrite due to poor English as well as a review based on our findings regarding meiosis.
This version is working using C++17 on a GNU/Linux system.
C++17 and better.
- CMake 3.13+ but >= 3.18 is recommended
- C++17 compiler
- gcc >= 10
- clang >= 15
- Optional for
lint
validation- clang-tidy >= 15
- Optional for
vscodium
integration- clangd >= 15
- clang-tools >= 15
- clang-format >= 15
- Optional
- libunwind8 >= 1.2.1
Installing build dependencies on Debian (11 or better):
apt install git
apt install build-essential g++ gcc libc-dev libpthread-stubs0-dev
apt install clang-15 clang-tidy-15 clangd-15 clang-tools-15 clang-format-15
apt install cmake cmake-extras extra-cmake-modules pkg-config
apt install libunwind8 libunwind-dev
apt install doxygen graphviz
Perhaps change the clang version-suffix of above clang install line to the appropriate version.
After complete clang installation, you might want to setup the latest version as your default. For Debian you can use this clang alternatives setup script.
The following is covered with a convenient build script.
For a generic build use:
CPU_COUNT=`getconf _NPROCESSORS_ONLN`
git clone --recurse-submodule git://jausoft.com/srv/scm/gentech.git
cd gentech
mkdir build
cd build
cmake ..
make -j $CPU_COUNT install doc
Our cmake configure has a number of options, cmake-gui or ccmake can show you all the options. The interesting ones are detailed below:
Changing install path from /usr/local to /usr
-DCMAKE_INSTALL_PREFIX=/usr
Building debug build:
-DDEBUG=ON
Building with clang and clang-tidy lint
validation
-DCMAKE_C_COMPILER=/usr/bin/clang
-DCMAKE_CXX_COMPILER=/usr/bin/clang++
-DCMAKE_CXX_CLANG_TIDY=/usr/bin/clang-tidy;-p;$rootdir/$build_dir
To build documentation run:
make doc
IDE integration configuration files are provided for
- Eclipse with extensions
- CDT or CDT @ eclipse.org
- Not used due to lack of subproject include file and symbol resolution:
CMake Support
, installC/C++ CMake Build Support
with IDorg.eclipse.cdt.cmake.feature.group
From the project root directory, prepare the Debug
folder using cmake
./scripts/eclipse-cmake-prepare.sh
The existing project setup is just using external build
via make
.
You can import the project to your workspace via File . Import...
and Existing Projects into Workspace
menu item.
For Eclipse one might need to adjust some setting in the .project
and .cproject
(CDT)
via Eclipse settings UI, but it should just work out of the box.
IDE integration configuration files are provided for
- VSCodium or VS Code with extensions
- vscode-clangd
- Notable,
.settings/org.eclipse.cdt.core.prefs
describes the clang-format setup for this extension.
- Notable,
- twxs.cmake
- ms-vscode.cmake-tools
- notskm.clang-tidy
- cschlosser.doxdocgen
- jerrygoyal.shortcut-menu-bar
- vscode-clangd
For VSCodium one might copy the example root-workspace file
to the parent folder of this project (note the filename change) and adjust the path
to your filesystem.
cp .vscode/gentech.code-workspace_example ../gentech.code-workspace
vi ../gentech.code-workspace
Then you can open it via File . Open Workspace from File...
menu item.
- All listed extensions are referenced in this workspace file to be installed via the IDE
- The local settings.json has
clang-tidy
enabled- If using
clang-tidy
is too slow, just remove it from the settings file. clangd
will still contain a good portion ofclang-tidy
checks
- If using
This genetic algorithm follows the natural process, see our compilation about meiosis (pdf).
Nature defines and constructs lifeforms with its genome. The genome is coded by it's chromosomes.
A chromosome is a chain of nucleotides, the elements of the chromosomes. In nature these nucleotides a represented with the following four bases: Adenine (A), Guanine (G), Cytosine (C) and Thymine (T). The different sequences of these nucleotides, bases, on the chromosome, does code the genome[2].
The nature optimizes it's lifeforms with different methods. One of these methods is the sexual reproduction, so called mating. While mating, the genome of the mating partners are mixed, this is called "crossing over" [1,2,3,6]. The result of the mix is the genome of the partners child(s). E.g.:
Father : A G C T A G | A G G G T C | A C T A G
Mother : A A C T C G | A G C G T G | T C T A C
------------------------------------------------------
1st Child: A G C T A G | A G C G T G | A C T A G
2nd Child: A A C T C G | A G G G T C | T C T A C
Besides the "normal" crossing over (homologous or symmetric crossing over[2]),
asymmetric crossing over exists[2].
Within the asymmetric crossing over, at least in the version
of this genetic algorithm, one child contains the whole
genome of both parents.
So a growing (length) of the chromosomes is possible.
During the reproduction process so called mutations are possible. This mutations modifies the sequence of chromosomes with the following possible ways:
Mutation : Nucleotides are changed randomized.
In the nature, e.g. by radioactive radiation[1,2,3,4,6].
Inversion : A segment of a chromosome is transferred in reversed
order (last in - first out) [2,6].
E.g.: A G T A | A G C A T | C A G T ==>
A G T A | T A C G A | C A G T .
Translocation : A segment of a chromosome is transferred
to a different position to the destination (progeny). [6]
E.g.: A G T A | A G C A T | C A G T ==>
A G | A G C A T | T A C A G T .
On chromosomes the genome is stored. The logical whit (minimal part) of this genome is called gene. The gene represents a segment of a chromosome, but the definition of this noun is not that sharp since this documentation was written in March 1994. A chromosome, e.g. with a length of 10 000 bases, contains not only usable (useful) information. So useless information is also within the chromosomes. The chromosome's genes are often fractional.
The segments of genes/chromosomes with useful information are called exons[2]. The segments of genes/chromosomes with useless/junk information are called introns[2].
The fractional genes/chromosomes are spliced (splicing[2]), before they are transferred and used for the working process, e.g. the production of protein. The results of splicing is the useful meaning information, non fractional extrons. So the working process receives just the (you can call this compressed) useful information.
Using this generation process, the nature is able to create new life forces (creatures). With or without purpose, well, this is a philosophical or theological matter.
The natural environment defines the viability of it's creatures.
Darwin's thesis says, that only the best of a population can prevail, so called "Survival of the Fittest".
This natural selection prefers consequently the best of a generation. These "best" are able to reproduce itself more often (than the "worse"), so they can take care of a better condition of it's progeny. The next generation is thus more optimized as its predecessor (may be). So it is possible, that a population creates it's next optimized version.
This natural evolution principle, describes with crossing over(symmetrical and asymmetrical), mutations, splicing and selection, is the role model for this genetic algorithm. Well, I think that I can think, so it may works ;-)
Under the terms of the natural principle of evolution a problem should be solved. The following steps are necessary:
-
Creation of a random starting population
-
Setting the normal fitness [0..1] to the spliced genome using a given fitness function. This fitness function is problem-oriented, and must be define for each problem
-
Select the parents according the best fitness (Survival of the Fittest).
-
Reproducing using the selected parents with crossing over(s).
-
Drop the not well conditioned members of the population, to make the population's size finite.
-
Mutate if necessary (statistically)
-
continue at point 2.
This look will be terminated, if the chosen target fitness is reached, or is a chosen number of non optimized generations in a row.
The selection (2) of the parents occurs with the roulette system. The better individuals receives higher probability as the worse individuals of the generation. The probability, that parents are composed outta individuals with a better fitness is most probably. But it is not impossible, that parents are composed outta individuals, which fitness may be worse at the current time. Herewith it is avoided, that currently questionable worse solutions are rejected.[1,3,4,6]
The decease within the population can be regulated in two ways. One way is to create a complete new generation[4], which replaces the parents generation. in this case, the birth rate equals one. The other way is to use a lower birth rate, e.g. 0.6. In this case 60 percent new individuals are created, whereby their parents must die. Because bigamous relationships are allowed for both methods, after the decease of the parents as much individuals with a worse fitness must die, as the population's maximum is not exceeded.
This natural analogue principle is declared in the file gentech.h, and defined in the file gentech.cpp.
The class 'Chromosome' contains the nucleotides of one chromosome, the methods for splicing and mutations besides others. For details, please have a look at the file gentech.h.
The class 'Chromosomes' (many chromosomes -> population) contains the methods for selection, crossing over and the whole evolution process.
The fitness method within the class 'Chromosomes' is a virtual one. The user, who want's to define the problem, must define this one regarding his problem. It must return a normal floating value within [0..1].
'How do I encode the problem within the chromosomes' ? Is the basic question, and it's answer the problem's solution.
For example: In the river-problem (see 1.3.1 below), the combination of the boat crew must be encoded.
The encoding is implemented to expose only valid crew combinations.
In this case, one nucleotide has the following range of values within [0..4]:
0 : 1 Monk
1 : 2 Monks
2 : 1 Cannibal
3 : 2 Cannibals
4 : 1 Monk and 1 Cannibal
An encoded (solution) chromosome of this kind, supplies the alternating boat crew from shore-a to shore b and vice versa.
The implementations of the game itself is contained within the files 'RIVER.[H|CPP]' using the class 'RiverGame'.
The chromosomes encoding of this game is contained within the files
src/gen-river/river_gen.(h|cpp)
.
Here you find the class 'RiverProblem' as a derivation of
the class 'Chromosomes'.
The river problem is that monks and cannibals must cross the river in an way, so that the cannibal number is never greater as the monk number on both riversides - except only cannibals exist on one riverside. The boat is able to transport up to two persons, but one person as the minimum.
The salesman-problem is that the salesman must travel to many towns in an way, so that he takes the shortest way. The difference to the river-problem (see river.gen) is that the solution is not clear ... meaning that the shortest way is unknown.
We wish you fun in solving problems following the methods of natural reproduction ;-)
This work was initially created
by Sven Gothel and Christian Mueller in February 1994
for a home assignment in Object-Oriented Programming (OOP)
at the FH Bielefeld (University for Applied Science)
under the supervision of Prof. Dr. Bunse.
See Changes.
[1] Holland, John H. : Genetische Algorithmen,
Spektrum der Wissenschaft, September 1992, S.44-51
[2] Chambon, Pierre : Gestueckelte Gene - ein Informations-Mosaik,
Spektrum der Wissenschaft, Juli 1981, S.104-117
[3] Dewdney, A.K. : Genetische Algorithmen,
Computer-Kurzweil, Spektrum-der-Wissenschaft-Verlagsgesellschaft
1988, ISBN 3-922508-50-2, S.68-72
[4] Weckwerth, Guido : Zeugende Zahlen,
MC, Oktober 1993, S.54-58, Januar 1994, S.72-75
[5] Schader, Kuhlins : Programmieren in C++,
Springer-Verlag Heidelberg 1993, ISBN 3-540-56524-8
[6] Schoeneburg, Eberhard : Genetische Algorithmen und Evolutionsstrategien
Addison-Wesley 1994, ISBN 3-89319-495-2