""" This example demonstrates how to remove all blend shape data from a DNA. IMPORTANT: You have to setup the environment before running this example. Please refer to the 'Environment setup' section in README.md. - usage in command line: python dnacalib_clear_blend_shapes.py mayapy dnacalib_clear_blend_shapes.py - usage in Maya: 1. copy whole content of this file to Maya Script Editor 2. change value of ROOT_DIR to absolute path of dna_calibration, e.g. `c:/dna_calibration` in Windows or `/home/user/dna_calibration`. Important: Use `/` (forward slash), because Maya uses forward slashes in path. - customization: - change CHARACTER_NAME to Taro, or the name of a custom DNA file placed in /data/dna_files Expected: Script will generate Ada_output.dna in OUTPUT_DIR from original Ada.dna. NOTE: If OUTPUT_DIR does not exist, it will be created. """ from os import makedirs from os import path as ospath # if you use Maya, use absolute path ROOT_DIR = f"{ospath.dirname(ospath.abspath(__file__))}/..".replace("\\", "/") OUTPUT_DIR = f"{ROOT_DIR}/output" CHARACTER_NAME = "Ada" DATA_DIR = f"{ROOT_DIR}/data" CHARACTER_DNA = f"{DATA_DIR}/dna_files/{CHARACTER_NAME}.dna" OUTPUT_DNA = f"{OUTPUT_DIR}/{CHARACTER_NAME}_output.dna" from dna import DataLayer_All, FileStream, Status, BinaryStreamReader, BinaryStreamWriter from dnacalib import ( DNACalibDNAReader, ClearBlendShapesCommand ) def load_dna(path): stream = FileStream(path, FileStream.AccessMode_Read, FileStream.OpenMode_Binary) reader = BinaryStreamReader(stream, DataLayer_All) reader.read() if not Status.isOk(): status = Status.get() raise RuntimeError(f"Error loading DNA: {status.message}") return reader def save_dna(reader, path): stream = FileStream(path, FileStream.AccessMode_Write, FileStream.OpenMode_Binary) writer = BinaryStreamWriter(stream) writer.setFrom(reader) writer.write() if not Status.isOk(): status = Status.get() raise RuntimeError(f"Error saving DNA: {status.message}") def validate_geometry(dna): mesh_count = dna.getMeshCount() for mesh_index in range(mesh_count): bs_tgt_count = dna.getBlendShapeTargetCount(mesh_index) for bs_tgt_index in range(bs_tgt_count): bs_tgt_delta_count = dna.getBlendShapeTargetDeltaCount(mesh_index, bs_tgt_index) if bs_tgt_delta_count != 0: raise RuntimeError("Blend shape target deltas not removed properly!") def validate_animation_data(dna): bs_channel_lods = dna.getBlendShapeChannelLODs() bs_channel_input_indices = dna.getBlendShapeChannelInputIndices() bs_channel_output_indices = dna.getBlendShapeChannelOutputIndices() if len(bs_channel_lods) != dna.getLODCount(): raise RuntimeError("Blend shape animation data not removed properly! Number of blend shape LODs does not match LOD count!") for lod in bs_channel_lods: if lod != 0: raise RuntimeError("Blend shape animation data not removed properly!") if (len(bs_channel_input_indices) != 0) or (len(bs_channel_output_indices) != 0): raise RuntimeError("Blend shape animation data not removed properly!") def calibrate_dna(input_path, output_path): dna = load_dna(input_path) # Copies DNA contents and will serve as input/output parameter to commands calibrated = DNACalibDNAReader(dna) mesh_count = calibrated.getMeshCount() print(f"Number of meshes: {mesh_count}") for mesh_index in range(mesh_count): bs_tgt_count = calibrated.getBlendShapeTargetCount(mesh_index) print(f"Number of blendshape targets for mesh {calibrated.getMeshName(mesh_index)}({mesh_index}): {bs_tgt_count}") for bs_tgt_index in range(bs_tgt_count): bs_tgt_delta_count = calibrated.getBlendShapeTargetDeltaCount(mesh_index, bs_tgt_index) print(f"Number of blendshape target deltas for mesh {calibrated.getMeshName(mesh_index)}({mesh_index}), blend shape target {bs_tgt_index}: {bs_tgt_delta_count}") print(f"Blend shape channel LODs: {calibrated.getBlendShapeChannelLODs()}") print(f"Blend shape channel input indices: {calibrated.getBlendShapeChannelInputIndices()}") print(f"Blend shape channel output indices: {calibrated.getBlendShapeChannelOutputIndices()}") # Clears all blend shapes command = ClearBlendShapesCommand() print("\n\nClearing blend shape data...\n\n") # Modifies calibrated DNA in-place command.run(calibrated) validate_geometry(calibrated) validate_animation_data(calibrated) print(f"Number of meshes: {mesh_count}") for mesh_index in range(mesh_count): bs_tgt_count = calibrated.getBlendShapeTargetCount(mesh_index) print(f"Number of blendshape targets for mesh {calibrated.getMeshName(mesh_index)}({mesh_index}): {bs_tgt_count}") for bs_tgt_index in range(bs_tgt_count): bs_tgt_delta_count = calibrated.getBlendShapeTargetDeltaCount(mesh_index, bs_tgt_index) print(f"Number of blendshape target deltas for mesh {calibrated.getMeshName(mesh_index)}({mesh_index}), blend shape target {bs_tgt_index}: {bs_tgt_delta_count}") bs_channel_lods = dna.getBlendShapeChannelLODs() bs_channel_input_indices = dna.getBlendShapeChannelInputIndices() bs_channel_output_indices = dna.getBlendShapeChannelOutputIndices() print(f"Blend shape channel LODs: {bs_channel_lods}") print(f"Blend shape channel input indices: {bs_channel_input_indices}") print(f"Blend shape channel output indices: {bs_channel_output_indices}") print("\n\nSuccessfully cleared blend shape data.") print("Saving DNA...") save_dna(calibrated, output_path) print("Done.") if __name__ == "__main__": makedirs(OUTPUT_DIR, exist_ok=True) calibrate_dna(CHARACTER_DNA, OUTPUT_DNA)