コード例 #1
0
def test_crossover1D_output_shape():
    POPULATION_SHAPE = (8, 6)
    population = B.randint(0, 1024, POPULATION_SHAPE)
    population_fraction = 0.5
    mutations_probability = 0.2

    original_population = copy(population)
    population = DualCrossover1D(population_fraction,
                                 mutations_probability,
                                 debug=True)(population)

    cprint(population, 'cyan')
    cprint(original_population, 'yellow')

    assert population.shape == POPULATION_SHAPE
    # measuring mutation rate
    diff = B.clip(abs(population - original_population), 0, 1)

    # row test
    num_ones_in_row = 0
    for col in diff:
        num_ones_in_row = max(list(col).count(1), num_ones_in_row)

    max_one_in_row = int(POPULATION_SHAPE[1] * mutations_probability)
    assert num_ones_in_row == max_one_in_row
    assert num_ones_in_row
コード例 #2
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ファイル: random_mutation.py プロジェクト: ameya7295/geneflow
    def call(self, populations):
        """ Create the mask use to generate mutations

        Args:
            population_shape (list): population tensor shape.
        Returns:
            tensor: mask

        Generation works by:
        1. creating a slice that contains the mutation
        2. Inserting it into the mask
        3. Shuffle the mask in every dimension to distribute them
        """
        results = []

        for population in populations:

            affected_population = int(population.shape[0] *
                                      self.population_fraction)

            # Build sub tensors & slices by iterating through tensor dimensions
            sub_tensor_shape = [affected_population]
            slices = [slice(0, affected_population)]
            for idx, pop_size in enumerate(population.shape[1:]):
                midx = idx - 1  # recall dim1 are genes.
                tsize = int(pop_size * self.mutations_probability[midx])
                sub_tensor_shape.append(tsize)
                slices.append(slice(0, tsize))
            slices = tuple(slices)
            self.print_debug("sub_tensor_shape", sub_tensor_shape)

            # drawing mutations
            mutations = B.randint(self.min_mutation_value,
                                  self.max_mutation_value + 1,
                                  shape=sub_tensor_shape)
            # blank mask
            mask = B.zeros(population.shape)

            # add mutations
            mask[slices] = mutations

            # shuffle mask every axis
            B.full_shuffle(mask)

            # mutate
            population = population + mask

            # normalize
            if self.max_gene_value or self.min_gene_value:
                self.print_debug("min_gen_val", self.min_gene_value)
                self.print_debug("max_gen_val", self.max_gene_value)

                population = B.clip(population,
                                    min_val=self.min_gene_value,
                                    max_val=self.max_gene_value)
            results.append(population)
        return results
コード例 #3
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def test_uniform_distribution():
    """check that every gene of the tensor are going to be flipped equally
    Note:
    # ! We need enough iterations and chromosomes to reduce collision
    # ! and ensure numerical stability
    """

    NUM_ITERATIONS = 1000
    GENOME_SHAPE = (20, 4, 4)
    population = B.randint(0, 1024, GENOME_SHAPE)
    population_fraction = 1
    crossover_probability = (0.5, 0.5)

    # each gene proba of being mutated 0.5*0.5 > 0.25
    # each chromosome proba of being mutated 1
    # => gene average hit rate: 1000 / (1/4)  ~250
    MIN_DIFF_BOUND = 200
    MAX_DIFF_BOUND = 300

    OP = RandomMutations2D(population_fraction, crossover_probability)

    # diff matrix
    previous_population = copy(population)
    population = OP(population)
    diff = B.clip(abs(population - previous_population), 0, 1)
    for _ in range(NUM_ITERATIONS - 1):
        previous_population = copy(population)
        population = OP(population)

        curr_diff = B.clip(abs(population - previous_population), 0, 1)
        # acumulating diff matrix
        diff += curr_diff

    print(curr_diff)

    for c in diff:
        print(c)
        print('mean', B.mean(c), 'min', B.min(c), 'max', B.max(c))
        assert B.min(c) > MIN_DIFF_BOUND
        assert B.max(c) < MAX_DIFF_BOUND
        assert MIN_DIFF_BOUND < B.mean(c) < MAX_DIFF_BOUND
コード例 #4
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def test_dualcrossover2d_distribution():
    """check that every gene of the tensor are going to be flipped equally
    Note:
    # ! We need enough iterations and chromosomes to reduce collision
    # ! and ensure numerical stability
    """
    NUM_ITERATIONS = 1000
    GENOME_SHAPE = (100, 4, 4)
    population = B.randint(0, 1024, GENOME_SHAPE)
    population_fraction = 1
    crossover_probability = (0.5, 0.5)

    OP = DualCrossover2D(population_fraction, crossover_probability)

    # diff matrix
    previous_population = copy(population)
    population = OP(population)
    diff = B.clip(abs(population - previous_population), 0, 1)
    print(diff)

    for _ in range(NUM_ITERATIONS - 1):
        previous_population = copy(population)
        population = OP(population)

        curr_diff = B.clip(abs(population - previous_population), 0, 1)
        # acumulating diff matrix
        diff += curr_diff

    # print(curr_diff)

    for c in diff:
        print(c)
        print('mean', B.mean(c), 'min', B.min(c), 'max', B.max(c))
        assert B.min(c) > 50
        assert B.max(c) < NUM_ITERATIONS / 2
        assert 200 < B.mean(c) < NUM_ITERATIONS / 2
コード例 #5
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def test_1D_shape():
    POPULATION_SHAPE = (64, 16)
    population = B.randint(0, 1024, POPULATION_SHAPE)
    population_fraction = 0.5
    crossover_size_fraction = 0.2

    original_population = copy(population)
    population = SingleCrossover1D(population_fraction,
                                   crossover_size_fraction,
                                   debug=1)(population)

    cprint(population, 'cyan')
    cprint(original_population, 'yellow')

    assert population.shape == POPULATION_SHAPE
    # measuring mutation rate
    diff = B.clip(abs(population - original_population), 0, 1)
    print(diff, 'cyan')

    # row test
    num_ones_in_row = 0
    for col in diff:
        num_ones = list(col).count(1)
        print(num_ones)
        num_ones_in_row = max(num_ones, num_ones_in_row)

    max_one_in_row = POPULATION_SHAPE[1] * crossover_size_fraction
    assert num_ones_in_row <= max_one_in_row
    assert num_ones_in_row

    # col
    diff = diff.T
    num_ones_in_col = 0
    for col in diff:
        num_ones_in_col = max(list(col).count(1), num_ones_in_col)

    max_one_in_col = POPULATION_SHAPE[0] * population_fraction
    assert max_one_in_col - 2 <= num_ones_in_col <= max_one_in_col
コード例 #6
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def test_uniform_2Dcrossover_randomness_shape():
    GENOME_SHAPE = (10, 4, 4)
    population = B.randint(0, 1024, GENOME_SHAPE)
    population_fraction = 0.5
    crossover_probability = (0.5, 0.5)

    original_population = copy(population)
    OP = UniformCrossover2D(population_fraction, crossover_probability)
    population = OP(population)

    diff = B.clip(abs(population - original_population), 0, 1)
    print(diff)
    expected_mutations = original_population.shape[0] * population_fraction

    mutated_chromosomes = []
    for c in diff:
        if B.max(c):
            mutated_chromosomes.append(c)
    num_mutations = len(mutated_chromosomes)

    # sometime we have a collision so we use a delta
    assert abs(num_mutations - expected_mutations) < 2

    mutated_rows = crossover_probability[0] * GENOME_SHAPE[1]
    mutated_cells = crossover_probability[0] * GENOME_SHAPE[2]
    for cidx, c in enumerate(mutated_chromosomes):
        mr = 0
        mc = 0
        for r in c:
            s = B.sum(r)
            if s:
                mr += 1
                mc += s

        assert abs(mutated_rows - mr) < 2
        assert abs(mutated_cells - (mc // mutated_rows)) < 2
コード例 #7
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    def __init__(self,
                 population_fraction=0.9,
                 crossover_probability=(0.2, 0.2, 0.2),
                 **kwargs):

        if len(crossover_probability) != 3:
            raise ValueError('crossover_probability must be of form (x, y, z)')

        super(DualCrossover3D,
              self).__init__(population_fraction=population_fraction,
                             crossover_probability=crossover_probability,
                             **kwargs)


if __name__ == '__main__':
    from copy import copy
    print(B.backend())
    GENOME_SHAPE = (6, 4, 4)
    population = B.randint(0, 256, GENOME_SHAPE)
    population_fraction = 0.5
    max_crossover_size_fraction = (0.5, 0.5)
    print(population.shape)
    original_population = copy(population)
    population = DualCrossover2D(population_fraction,
                                 max_crossover_size_fraction,
                                 debug=True)(population)

    # diff matrix
    diff = B.clip(abs(population - original_population), 0, 1)
    print(diff)
コード例 #8
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if __name__ == '__main__':
    from copy import copy
    print(B.backend())
    GENOME_SHAPE = (10, 4, 4)
    population = B.randint(0, 1024, GENOME_SHAPE)
    population_fraction = 0.5
    crossover_probability = (0.5, 0.5)

    print(population.shape)
    # peforming crossover
    original_population = copy(population)
    population = UniformCrossover2D(population_fraction,
                                    crossover_probability)(population)

    # diff matrix
    diff = B.clip(abs(population - original_population), 0, 1)
    print(diff)
    # expected mutated chromosomes
    expected_mutated = population.shape[0] * population_fraction
    cprint(
        "Expected mutated chromosome:%d (+/- 1 due to collision)" %
        (expected_mutated), 'cyan')
    # select mutated chromosomes
    mutated_chromosomes = []
    for c in diff:
        if B.max(c):
            mutated_chromosomes.append(c)
    cprint("mutated chromosome:%d" % (len(mutated_chromosomes)), 'magenta')

    cprint("[example of mutated chromosome]", 'yellow')
    cprint(mutated_chromosomes[0], 'cyan')