genoxide for Python
Evolutionary computation in Rust, for Python: genetic algorithms, local search, differential evolution, CMA-ES, particle swarm optimization, and NSGA-II, NSGA-III, SPEA2, MOEA/D and SMS-EMOA for several objectives, from genoxide, with fitness functions in Python and numpy.
import numpy as np
import genoxide as gx
# OneMax: the genome with the most ones
ga = gx.Ga(
gx.Binary(100),
population_size=100,
select=gx.Tournament(3),
crossover=gx.UniformCrossover(),
mutation=gx.BitFlip(rate=0.01),
seed=42,
)
result = ga.run(lambda bits: bits.sum(), target=100, generations=1_000)
print(result.best_fitness, result.generations)
# Rastrigin with CMA-ES and IPOP restarts, a generation per call
def rastrigin(x): # x: a genome per row
return 10 * x.shape[1] + np.sum(x**2 - 10 * np.cos(2 * np.pi * x), axis=1)
cmaes = gx.Cmaes(gx.Real((-5.12, 5.12), length=10), restarts="ipop", objective="minimize", seed=1)
result = cmaes.run(rastrigin, batch=True, target=1e-8, evaluations=500_000)
print(result.best_genome, result.best_fitness)
More in examples/: OneMax, a knapsack with a constraint, N-Queens with tabu search, Rastrigin with CMA-ES and L-SHADE, and ZDT1 with NSGA-II.
Install
pip install genoxide
The wheels are for Linux (x86_64 and aarch64, glibc and musl), macOS (Apple silicon and Intel) and Windows (x64), and CPython 3.10 or later, with numpy. To build it from the repository instead, with Rust and maturin:
cd python
pip install maturin
maturin develop --release
Fitness functions
A fitness function takes a genome as a numpy array:
| Genome | Array |
|---|---|
Binary(length) |
bool |
Integer(bounds, length) |
int64 |
Real(bounds, length) |
float64 |
Permutation(length) |
int64, an ordering of 0 .. length - 1 |
bounds is one pair (low, high) for every gene, with length, or a list of pairs, one per gene.
It returns one of these:
- a number
Noneor NaN, for a solution that can't be scored(score, constraint_violation): infeasible solutions, with a positive violation, rank below feasible ones, and among themselves by violation (Deb's rules)
The fitness function must be deterministic: genoxide doesn't evaluate a child identical to one of its parents again.
With batch=True, the function takes a whole generation as a 2-D array, a genome per row, and returns an array of scores, or a tuple of scores and constraint violations. It's one call per generation (none for a generation whose children are all copies of their parents), so vectorized numpy, a GPU or a remote service pays its cost per call once per generation instead of once per genome.
With parallel=True, genoxide calls a function that isn't a batch function from several threads at once. It pays off when the function releases the GIL, e.g. in numpy on large arrays or waiting for I/O, or on free-threaded Python.
An exception in the fitness function stops the run and is raised by run, and so is Ctrl+C.
Algorithms
| Algorithm | Genomes | Settings |
|---|---|---|
Ga |
all | population_size, select, crossover, mutation, crossover_rate (0.9), mutation_rate (1), scheme |
LocalSearch |
all | neighbor (a mutation), neighbors (1), acceptance, restart=(patience, kicks) |
De |
real | population_size (the number of genes + 10), l_shade (a budget of evaluations, for L-SHADE) |
Cmaes |
real | population_size, restarts ("ipop", "bipop"), initial_step |
Pso |
real | population_size (needed), ring (neighbors on each side) |
Nsga2 |
all | objectives, population_size, crossover, mutation, crossover_rate (0.9), mutation_rate (1) |
Nsga3 |
all | objectives, reference_directions, crossover, mutation, population_size (the number of reference directions), crossover_rate (1), mutation_rate (1) |
Spea2 |
all | objectives, population_size (the archive's), crossover, mutation, crossover_rate (0.9), mutation_rate (1) |
Moead |
all | objectives, weights (a subproblem each), crossover, mutation, decomposition (Tchebycheff()), neighbors (20), neighbor_mating (0.9), max_replacements (2), crossover_rate (1), mutation_rate (1) |
SmsEmoa |
all | objectives, population_size, crossover, mutation, offspring (population_size), crossover_rate (0.9), mutation_rate (1) |
Single-objective algorithms maximize, or minimize with objective="minimize". The multi-objective algorithms take objectives=["minimize", "maximize", ...], 2 to 6 of them. Their fitness function returns a sequence of objective values, and their result is the final non-dominated front: front_genomes, front_objectives and front_violations.
Nsga2spreads the front by crowding distance, which works poorly beyond 2 or 3 objectives.Nsga3spreads it along reference directions instead, andMoeadsolves a single-objective subproblem per weight vector.das_dennis(objectives, divisions)gives evenly spread directions or weights, a row each: 91 for 3 objectives and 12 divisions.Spea2keeps an archive of the best solutions, the non-dominated ones first, truncated by the distance to their nearest neighbors.Nsga2,Nsga3,Spea2andSmsEmoadrop a child that equals a member of the population or an earlier child, and breed another, as pymoo does:eliminate_duplicates=Falsekeeps copies.SmsEmoaremoves, from the last front that fits partly, the solutions that contribute the least hypervolume. It costs more per generation thanNsga2: O(N log N) per removal for 2 objectives, O(N²) for 3, O(N³) for 4 and O(N⁴) for 5, whereNsga3orMoeadare better choices.
Every algorithm takes a seed: the same seed repeats a run exactly, with a genome at a time, in batches or in parallel.
Operators:
- Selection:
Tournament(size),Rank(pressure),Roulette(),StochasticUniversalSampling(),Truncation(fraction),RandomSelection() - Crossover:
- any list genome:
UniformCrossover(),PointCrossover(points),NoCrossover() - real genomes:
SimulatedBinaryCrossover(eta),BlendCrossover(alpha),ArithmeticCrossover() - permutations:
OrderCrossover(),PartiallyMappedCrossover(),CycleCrossover(),EdgeRecombinationCrossover()
- any list genome:
- Mutation:
- binary genomes:
BitFlip(rate=... | count=...) - integer and real genomes:
UniformMutation(rate=... | count=...) - real genomes:
GaussianMutation(sigma, rate=... | count=...),PolynomialMutation(eta, rate=... | count=...) - permutations:
SwapMutation(count),InversionMutation(),InsertionMutation(),ScrambleMutation()
- binary genomes:
- Genetic algorithm schemes:
Generational(elitism)(the default, with 1),SteadyState(replacements),MuPlusLambda(offspring),MuCommaLambda(offspring) - Local search acceptance:
NotWorse()(the default),Improving(),Annealing(initial_temperature, cooling),Tabu(tenure) - MOEA/D decomposition:
Tchebycheff()(the default),Pbi(theta)(penalty-based boundary intersection,theta5 by default), which spreads fronts of 3 or more objectives well
Stopping
run stops at the first of its stop conditions, and needs at least one:
generationsevaluationstarget: a score at least as good (single objective)time: secondsstagnation: generations without improvement
The result says which one stopped it, in stop_reason, with the numbers of generations and evaluations and the seconds it took.
Progress
run(..., on_generation=callback) calls callback after every generation, the initial population (generation 0) included, on the thread that called run. It gets a read-only Progress with the generation, the evaluations and the seconds so far, and the best_fitness so far (None before a valid solution); for a multi-objective algorithm, a MultiProgress with the front_size (the number of non-dominated individuals in the population) instead.
If callback returns False, the run stops with the stop reason "aborted". If it raises an exception, the run stops and run raises it.
def report(progress):
if progress.generation % 100 == 0:
print(progress.generation, progress.evaluations, progress.best_fitness)
result = ga.run(lambda bits: bits.sum(), generations=1_000, on_generation=report)
Release files for genoxide 0.6.0
For a detailed explanation of source distributions (sdists) and built distributions (wheels), please see the package formats documentation.
Source distribution (sdist)
| File | Size | Uploaded | |
|---|---|---|---|
| genoxide-0.6.0.tar.gz | 337.3 kB | Details |
Built distributions (wheels)
| File | Reset | |||
|---|---|---|---|---|
| genoxide-0.6.0-cp310-abi3-win_amd64.whl | CPython 3.10 | abi3 | Windows x86-64 | Details |
| genoxide-0.6.0-cp310-abi3-musllinux_1_2_x86_64.whl | CPython 3.10 | abi3 | Linux musl 1.2+ x86-64 | Details |
| genoxide-0.6.0-cp310-abi3-musllinux_1_2_aarch64.whl | CPython 3.10 | abi3 | Linux musl 1.2+ ARM64 | Details |
| genoxide-0.6.0-cp310-abi3-manylinux_2_17_x86_64.manylinux2014_x86_64.whl | CPython 3.10 | abi3 | Linux glibc 2.17+ x86-64 | Details |
| genoxide-0.6.0-cp310-abi3-manylinux_2_17_aarch64.manylinux2014_aarch64.whl | CPython 3.10 | abi3 | Linux glibc 2.17+ ARM64 | Details |
| genoxide-0.6.0-cp310-abi3-macosx_11_0_arm64.whl | CPython 3.10 | abi3 | macOS 11.0+ ARM64 | Details |
| genoxide-0.6.0-cp310-abi3-macosx_10_12_x86_64.whl | CPython 3.10 | abi3 | macOS 10.12+ x86-64 | Details |
Total release size: 16.1 MB
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