source: framspy/FramsticksLib.py @ 1215

from typing import List  # to be able to specify a type hint of list(something)
import json
import sys, os
import argparse
import numpy as np
import frams


class FramsticksLib:
        """Communicates directly with Framsticks library (.dll or .so or .dylib).
        You can perform basic operations like mutation, crossover, and evaluation of genotypes.
        This way you can perform evolution controlled by python as well as access and manipulate genotypes.
        You can even design and use in evolution your own genetic representation implemented entirely in python,
        or access and control the simulation and simulated creatures step by step.

        Should you want to modify or extend this class, first see and test the examples in frams-test.py.

        You need to provide one or two parameters when you run this class: the path to Framsticks where .dll/.so/.dylib resides
        and, optionally, the name of the Framsticks dll/so/dylib (if it is non-standard). See::
                FramsticksLib.py -h"""

        PRINT_FRAMSTICKS_OUTPUT: bool = False  # set to True for debugging
        DETERMINISTIC: bool = False  # set to True to have the same results in each run

        GENOTYPE_INVALID = "/*invalid*/"  # this is how genotype invalidity is represented in Framsticks
        EVALUATION_SETTINGS_FILE = [  # all files MUST be compatible with the standard-eval expdef. The order they are loaded in is important!
                "eval-allcriteria.sim",  # a good trade-off in performance sampling period ("perfperiod") for vertpos and velocity
                # "deterministic.sim",  # turns off random noise (added for robustness) so that each evaluation yields identical performance values (causes "overfitting")
                # "sample-period-2.sim", # short performance sampling period so performance (e.g. vertical position) is sampled more often
                # "sample-period-longest.sim",  # increased performance sampling period so distance and velocity are measured rectilinearly
        ]


        # This function is not needed because in Python, "For efficiency reasons, each module is only imported once per interpreter session."
        # @staticmethod
        # def getFramsModuleInstance():
        #       """If some other party needs access to the frams module to directly access or modify Framsticks objects,
        #       use this function to avoid importing the "frams" module multiple times and avoid potentially initializing
        #       it many times."""
        #       return frams

        def __init__(self, frams_path, frams_lib_name, sim_settings_files):
                if frams_lib_name is None:
                        frams.init(frams_path)  # could add support for setting alternative directories using -D and -d
                else:
                        frams.init(frams_path, "-L" + frams_lib_name)  # could add support for setting alternative directories using -D and -d

                print('Available objects:', dir(frams))
                print()

                simplest = self.getSimplest("1")
                if not (simplest == "X" and type(simplest) is str):
                        raise RuntimeError('Failed getSimplest() test.')
                if not (self.isValid(["X[0:0],", "X[0:0]", "X[1:0]"]) == [False, True, False]):
                        raise RuntimeError('Failed isValid() test.')

                if not self.DETERMINISTIC:
                        frams.Math.randomize()
                frams.Simulator.expdef = "standard-eval"  # this expdef (or fully compatible) must be used by EVALUATION_SETTINGS_FILE
                if sim_settings_files is not None:
                        self.EVALUATION_SETTINGS_FILE = sim_settings_files.split(";")  # overwrite defaults
                print('Basic tests OK. Using settings:', self.EVALUATION_SETTINGS_FILE)
                print()
                if not isinstance(self.EVALUATION_SETTINGS_FILE, list):  # ensure settings file(s) are provided as a list
                        raise ValueError("Evaluation settings file(s) '%s' should be provided as a list" % self.EVALUATION_SETTINGS_FILE)

                for simfile in self.EVALUATION_SETTINGS_FILE:
                        ec = frams.MessageCatcher.new()  # catch potential errors, warnings, messages - just to detect if there are ERRORs
                        ec.store = 2;  # store all, because they are caught by MessageCatcher and will not appear in output (which we want)
                        frams.Simulator.ximport(simfile, 4 + 8 + 16)
                        ec.close()
                        print(ec.messages)  # output all caught messages
                        if ec.error_count._value() > 0:
                                raise ValueError("Problem while importing file '%s'" % simfile)  # make missing files or incorrect paths fatal because error messages are easy to overlook in output, and these errors would not prevent Framsticks simulator from performing genetic operations, starting and running in evaluate()


        def getSimplest(self, genetic_format) -> str:
                return frams.GenMan.getSimplest(genetic_format).genotype._string()


        def evaluate(self, genotype_list: List[str]):
                """
                Returns:
                        List of dictionaries containing the performance of genotypes evaluated using self.EVALUATION_SETTINGS_FILE.
                        Note that for whatever reason (e.g. incorrect genotype), the dictionaries you will get may be empty or
                        partially empty and may not have the fields you expected, so handle such cases properly.
                """
                assert isinstance(genotype_list, list)  # because in python, str has similar capabilities as list and here it would pretend to work too, so to avoid any ambiguity

                if not self.PRINT_FRAMSTICKS_OUTPUT:
                        ec = frams.MessageCatcher.new()  # mute potential errors, warnings, messages
                        ec.store = 2;  # store all, because they are caught by MessageCatcher and will not appear in output

                frams.GenePools[0].clear()
                for g in genotype_list:
                        frams.GenePools[0].add(g)
                frams.ExpProperties.evalsavefile = ""  # no need to store results in a file - we will get evaluations directly from Genotype's "data" field
                frams.Simulator.init()
                frams.Simulator.start()

                # step = frams.Simulator.step  # cache reference to avoid repeated lookup in the loop (just for performance)
                # while frams.Simulator.running._int():  # standard-eval.expdef sets running to 0 when the evaluation is complete
                #       step()
                frams.Simulator.eval("while(Simulator.running) Simulator.step();")  # fastest
                # Timing for evaluating a single simple creature 100x:
                # - python step without caching: 2.2s
                # - python step with caching   : 1.6s
                # - pure FramScript and eval() : 0.4s

                if not self.PRINT_FRAMSTICKS_OUTPUT:
                        ec.close()
                        if ec.error_count._value() > 0:
                                print(ec.messages)  # if errors occurred, output all caught messages for debugging
                                raise RuntimeError("[ERROR] %d error(s) and %d warning(s) while evaluating %d genotype(s)" % (ec.error_count._value(), ec.warning_count._value() - ec.error_count._value(), len(genotype_list)))  # make errors fatal; by default they stop the simulation anyway so let's not use potentially incorrect or partial results and fix the cause first.

                results = []
                for g in frams.GenePools[0]:
                        serialized_dict = frams.String.serialize(g.data[frams.ExpProperties.evalsavedata._value()])
                        evaluations = json.loads(serialized_dict._string())  # Framsticks native ExtValue's get converted to native python types such as int, float, list, str.
                        # now, for consistency with FramsticksCLI.py, add "num" and "name" keys that are missing because we got data directly from Genotype, not from the file produced by standard-eval.expdef's function printStats(). What we do below is what printStats() does.
                        result = {"num": g.num._value(), "name": g.name._value(), "evaluations": evaluations}
                        results.append(result)

                return results


        def mutate(self, genotype_list: List[str]) -> List[str]:
                """
                Returns:
                        The genotype(s) of the mutated source genotype(s). self.GENOTYPE_INVALID for genotypes whose mutation failed (for example because the source genotype was invalid).
                """
                assert isinstance(genotype_list, list)  # because in python, str has similar capabilities as list and here it would pretend to work too, so to avoid any ambiguity

                mutated = []
                for g in genotype_list:
                        mutated.append(frams.GenMan.mutate(frams.Geno.newFromString(g)).genotype._string())
                if len(genotype_list) != len(mutated):
                        raise RuntimeError("Submitted %d genotypes, received %d mutants" % (len(genotype_list), len(mutated)))
                return mutated


        def crossOver(self, genotype_parent1: str, genotype_parent2: str) -> str:
                """
                Returns:
                        The genotype of the offspring. self.GENOTYPE_INVALID if the crossing over failed.
                """
                return frams.GenMan.crossOver(frams.Geno.newFromString(genotype_parent1), frams.Geno.newFromString(genotype_parent2)).genotype._string()


        def dissimilarity(self, genotype_list: List[str], method: int) -> np.ndarray:
                """
                        :param method: -1 = genetic Levenshtein distance; 0, 1, 2 = phenetic dissimilarity (SimilMeasureGreedy, SimilMeasureHungarian, SimilMeasureDistribution)
                        :return: A square array with dissimilarities of each pair of genotypes.
                """
                assert isinstance(genotype_list, list)  # because in python, str has similar capabilities as list and here it would pretend to work too, so to avoid any ambiguity

                # if you want to override what EVALUATION_SETTINGS_FILE sets, you can do it below:
                # frams.SimilMeasureHungarian.simil_partgeom = 1
                # frams.SimilMeasureHungarian.simil_weightedMDS = 1

                n = len(genotype_list)
                square_matrix = np.zeros((n, n))

                if method in (0, 1, 2):  # Framsticks phenetic dissimilarity methods
                        frams.SimilMeasure.simil_type = method
                        genos = []  # prepare an array of Geno objects so that we don't need to convert raw strings to Geno objects all the time in loops
                        for g in genotype_list:
                                genos.append(frams.Geno.newFromString(g))
                        frams_evaluateDistance = frams.SimilMeasure.evaluateDistance  # cache function reference for better performance in loops
                        for i in range(n):
                                for j in range(n):  # maybe calculate only one triangle if you really need a 2x speedup
                                        square_matrix[i][j] = frams_evaluateDistance(genos[i], genos[j])._double()
                elif method == -1:
                        import Levenshtein
                        for i in range(n):
                                for j in range(n):  # maybe calculate only one triangle if you really need a 2x speedup
                                        square_matrix[i][j] = Levenshtein.distance(genotype_list[i], genotype_list[j])
                else:
                        raise Exception("Don't know what to do with dissimilarity method = %d" % method)

                for i in range(n):
                        assert square_matrix[i][i] == 0, "Not a correct dissimilarity matrix, diagonal expected to be 0"
                non_symmetric_diff = square_matrix - square_matrix.T
                non_symmetric_count = np.count_nonzero(non_symmetric_diff)
                if non_symmetric_count > 0:
                        non_symmetric_diff_abs = np.abs(non_symmetric_diff)
                        max_pos1d = np.argmax(non_symmetric_diff_abs)  # location of the largest discrepancy
                        max_pos2d_XY = np.unravel_index(max_pos1d, non_symmetric_diff_abs.shape)  # 2D coordinates of the largest discrepancy
                        max_pos2d_YX = max_pos2d_XY[1], max_pos2d_XY[0]  # 2D coordinates of the largest discrepancy mirror
                        worst_guy_XY = square_matrix[max_pos2d_XY]  # this distance and the other below (its mirror) are most different
                        worst_guy_YX = square_matrix[max_pos2d_YX]
                        print("[WARN] Dissimilarity matrix: expecting symmetry, but %g out of %d pairs were asymmetrical, max difference was %g (%g %%)" %
                              (non_symmetric_count / 2,
                               n * (n - 1) / 2,
                               non_symmetric_diff_abs[max_pos2d_XY],
                               non_symmetric_diff_abs[max_pos2d_XY] * 100 / ((worst_guy_XY + worst_guy_YX) / 2)))  # max diff is not necessarily max %
                return square_matrix


        def isValid(self, genotype_list: List[str]) -> List[bool]:
                """
                :returns: genetic validity (i.e., not based on trying to build creatures from provided genotypes). For a more thorough check, see isValidCreature().
                """
                assert isinstance(genotype_list, list)  # because in python, str has similar capabilities as list and here it would pretend to work too, so to avoid any ambiguity
                valid = []
                for g in genotype_list:
                        valid.append(frams.Geno.newFromString(g).is_valid._int() == 1)
                if len(genotype_list) != len(valid):
                        raise RuntimeError("Tested %d genotypes, received %d validity values" % (len(genotype_list), len(valid)))
                return valid


def parseArguments():
        parser = argparse.ArgumentParser(description='Run this program with "python -u %s" if you want to disable buffering of its output.' % sys.argv[0])
        parser.add_argument('-path', type=ensureDir, required=True, help='Path to the Framsticks library (.dll or .so or .dylib) without trailing slash.')
        parser.add_argument('-lib', required=False, help='Library name. If not given, "frams-objects.dll" (or .so or .dylib) is assumed depending on the platform.')
        parser.add_argument('-simsettings', required=False, help="The name of the .sim file with settings for evaluation, mutation, crossover, and similarity estimation. If not given, \"eval-allcriteria.sim\" is assumed by default. Must be compatible with the \"standard-eval\" expdef. If you want to provide more files, separate them with a semicolon ';'.")
        parser.add_argument('-genformat', required=False, help='Genetic format for the demo run, for example 4, 9, or S. If not given, f1 is assumed.')
        return parser.parse_args()


def ensureDir(string):
        if os.path.isdir(string):
                return string
        else:
                raise NotADirectoryError(string)


if __name__ == "__main__":
        # A demo run.

        # TODO ideas:
        # - check_validity with three levels (invalid, corrected, valid)
        # - a pool of binaries running simultaneously, balance load - in particular evaluation

        parsed_args = parseArguments()
        framsLib = FramsticksLib(parsed_args.path, parsed_args.lib, parsed_args.simsettings)

        print("Sending a direct command to Framsticks library that calculates \"4\"+2 yields", frams.Simulator.eval("return \"4\"+2;"))

        simplest = framsLib.getSimplest('1' if parsed_args.genformat is None else parsed_args.genformat)
        print("\tSimplest genotype:", simplest)
        parent1 = framsLib.mutate([simplest])[0]
        parent2 = parent1
        MUTATE_COUNT = 10
        for x in range(MUTATE_COUNT):  # example of a chain of 10 mutations
                parent2 = framsLib.mutate([parent2])[0]
        print("\tParent1 (mutated simplest):", parent1)
        print("\tParent2 (Parent1 mutated %d times):" % MUTATE_COUNT, parent2)
        offspring = framsLib.crossOver(parent1, parent2)
        print("\tCrossover (Offspring):", offspring)
        print('\tDissimilarity of Parent1 and Offspring:', framsLib.dissimilarity([parent1, offspring], 1)[0, 1])
        print('\tPerformance of Offspring:', framsLib.evaluate([offspring]))
        print('\tValidity (genetic) of Parent1, Parent 2, and Offspring:', framsLib.isValid([parent1, parent2, offspring]))