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IR/gen_meta_file.py ADDED
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+ import os
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+ import sys
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+ import json
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+ import pandas as pd
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+ import numpy as np
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+ from tqdm import tqdm
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+
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+ import rdkit
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+ from rdkit import Chem
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+ from rdkit.Chem import AllChem
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+
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+ sys.path.append("../../")
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+ from utils.compound_tools import mol_to_geognn_graph_data_MMFF3d
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+
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+
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+ def GetIRMetaFile():
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+ # get dataset_all, smiles_all, index_all from SMILES in IR dataset
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+
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+ raw_smiles_all, raw_index_all = [], []
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+ max_len = -1
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+ ir_filelist = os.listdir("./qm9_ir_spec/")
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+ for filename in tqdm(ir_filelist[:max_len]):
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+ mol_info = json.load(open(os.path.join("./qm9_ir_spec/", filename), "r"))
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+ raw_smiles_all.append(mol_info['smiles'])
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+ raw_index_all.append(filename.split('.')[0])
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+
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+ dataset_all, smiles_all, index_all = [], [], []
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+
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+ for i in tqdm(range(len(raw_smiles_all))):
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+ mol = AllChem.MolFromSmiles(raw_smiles_all[i])
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+ mol = Chem.AddHs(mol)
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+ AllChem.EmbedMolecule(mol)
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+ try:
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+ data = mol_to_geognn_graph_data_MMFF3d(mol)
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+ dataset_all.append(data); smiles_all.append(raw_smiles_all[i])
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+ index_all.append(raw_index_all[i])
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+ except ValueError:
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+ print("error in {}".format(i))
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+
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+ result_dict = dict(
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+ smiles_all=smiles_all, index_all=index_all,
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+ dataset_all=dataset_all,
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+ )
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+ np.save(f"ir_column_charity_all.npy", result_dict)
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+
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+ if __name__ == "__main__":
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+ GetIRMetaFile()
IR/ir_column_charity_100.npy ADDED
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+ version https://git-lfs.github.com/spec/v1
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+ oid sha256:b55c598dda0547cac6e919284a8bffaa0454df77a00694af9d82a902a6413906
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+ size 1195616
IR/ir_column_charity_10000.npy ADDED
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+ oid sha256:ce423c6832347e54342ed210de190f6bebc957ca164056b0707f966fe6a7f63f
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+ size 129309557
IR/ir_column_charity_all.npy ADDED
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+ version https://git-lfs.github.com/spec/v1
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+ oid sha256:82492d0812a79ad38394c07fc59be940676a865237bec4a69f98375c20d30991
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+ size 1528483538
IR/readme.txt ADDED
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+ gen_meta_file.py
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+ 用于根据IR数据集的smiles值生成 GeoGNN 能够处理的分子feature