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sample_split.py
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sample_split.py
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import argparse
import os
import shutil
import time
import numpy as np
import torch
from torch_geometric.data import Batch
from torch_geometric.transforms import Compose
from torch_scatter import scatter_sum, scatter_mean
from tqdm.auto import tqdm
import utils.misc as misc
import utils.transforms as trans
from datasets import get_dataset
from datasets.pl_data import FOLLOW_BATCH
from models.molopt_score_model import ScorePosNet3D, log_sample_categorical
from utils.evaluation import atom_num
from graphbap.bapnet import BAPNet
def unbatch_v_traj(ligand_v_traj, n_data, ligand_cum_atoms):
all_step_v = [[] for _ in range(n_data)]
for v in ligand_v_traj: # step_i
v_array = v.cpu().numpy()
for k in range(n_data):
all_step_v[k].append(v_array[ligand_cum_atoms[k]:ligand_cum_atoms[k + 1]])
all_step_v = [np.stack(step_v) for step_v in all_step_v] # num_samples * [num_steps, num_atoms_i]
return all_step_v
def sample_diffusion_ligand(model, data, num_samples, batch_size=16, device='cuda:0',
num_steps=None, pos_only=False, center_pos_mode='protein',
sample_num_atoms='prior', net_cond=None, cond_dim=128):
all_pred_pos, all_pred_v = [], []
all_pred_pos_traj, all_pred_v_traj = [], []
all_pred_v0_traj, all_pred_vt_traj = [], []
time_list = []
num_batch = int(np.ceil(num_samples / batch_size))
current_i = 0
for i in tqdm(range(num_batch)):
n_data = batch_size if i < num_batch - 1 else num_samples - batch_size * (num_batch - 1)
batch = Batch.from_data_list([data.clone() for _ in range(n_data)], follow_batch=FOLLOW_BATCH).to(device)
t1 = time.time()
with torch.no_grad():
batch_protein = batch.protein_element_batch
if sample_num_atoms == 'prior':
pocket_size = atom_num.get_space_size(batch.protein_pos.detach().cpu().numpy())
ligand_num_atoms = [atom_num.sample_atom_num(pocket_size).astype(int) for _ in range(n_data)]
batch_ligand = torch.repeat_interleave(torch.arange(n_data), torch.tensor(ligand_num_atoms)).to(device)
elif sample_num_atoms == 'range':
ligand_num_atoms = list(range(current_i + 1, current_i + n_data + 1))
batch_ligand = torch.repeat_interleave(torch.arange(n_data), torch.tensor(ligand_num_atoms)).to(device)
elif sample_num_atoms == 'ref':
batch_ligand = batch.ligand_element_batch
ligand_num_atoms = scatter_sum(torch.ones_like(batch_ligand), batch_ligand, dim=0).tolist()
else:
raise ValueError
# init ligand pos
center_pos = scatter_mean(batch.protein_pos, batch_protein, dim=0)
batch_center_pos = center_pos[batch_ligand]
init_ligand_pos = batch_center_pos + torch.randn_like(batch_center_pos)
# init ligand v
if pos_only:
init_ligand_v = batch.ligand_atom_feature_full
else:
uniform_logits = torch.zeros(len(batch_ligand), model.num_classes).to(device)
init_ligand_v = log_sample_categorical(uniform_logits)
r = model.sample_diffusion(
protein_pos=batch.protein_pos,
protein_v=batch.protein_atom_feature.float(),
batch_protein=batch_protein,
init_ligand_pos=init_ligand_pos,
init_ligand_v=init_ligand_v,
batch_ligand=batch_ligand,
num_steps=num_steps,
pos_only=pos_only,
center_pos_mode=center_pos_mode,
net_cond=net_cond,
cond_dim=cond_dim
)
ligand_pos, ligand_v, ligand_pos_traj, ligand_v_traj = r['pos'], r['v'], r['pos_traj'], r['v_traj']
ligand_v0_traj, ligand_vt_traj = r['v0_traj'], r['vt_traj']
# unbatch pos
ligand_cum_atoms = np.cumsum([0] + ligand_num_atoms)
ligand_pos_array = ligand_pos.cpu().numpy().astype(np.float64)
all_pred_pos += [ligand_pos_array[ligand_cum_atoms[k]:ligand_cum_atoms[k + 1]] for k in
range(n_data)] # num_samples * [num_atoms_i, 3]
all_step_pos = [[] for _ in range(n_data)]
for p in ligand_pos_traj: # step_i
p_array = p.cpu().numpy().astype(np.float64)
for k in range(n_data):
all_step_pos[k].append(p_array[ligand_cum_atoms[k]:ligand_cum_atoms[k + 1]])
all_step_pos = [np.stack(step_pos) for step_pos in
all_step_pos] # num_samples * [num_steps, num_atoms_i, 3]
all_pred_pos_traj += [p for p in all_step_pos]
# unbatch v
ligand_v_array = ligand_v.cpu().numpy()
all_pred_v += [ligand_v_array[ligand_cum_atoms[k]:ligand_cum_atoms[k + 1]] for k in range(n_data)]
all_step_v = unbatch_v_traj(ligand_v_traj, n_data, ligand_cum_atoms)
all_pred_v_traj += [v for v in all_step_v]
if not pos_only:
all_step_v0 = unbatch_v_traj(ligand_v0_traj, n_data, ligand_cum_atoms)
all_pred_v0_traj += [v for v in all_step_v0]
all_step_vt = unbatch_v_traj(ligand_vt_traj, n_data, ligand_cum_atoms)
all_pred_vt_traj += [v for v in all_step_vt]
t2 = time.time()
time_list.append(t2 - t1)
current_i += n_data
return all_pred_pos, all_pred_v, all_pred_pos_traj, all_pred_v_traj, all_pred_v0_traj, all_pred_vt_traj, time_list
if __name__ == '__main__':
root_dir = '/home/huangzl/workspace2/IPDiff-gspbapv5comp-n05'
parser = argparse.ArgumentParser()
parser.add_argument('--config', type=str, default=root_dir + '/configs/sampling.yml')
parser.add_argument('--train_config', type=str, default=root_dir + '/configs/training.yml')
parser.add_argument('--device', type=str, default='cuda:0')
parser.add_argument('--batch_size', type=int, default=25)
parser.add_argument('--result_path', type=str, default=root_dir + '/sampled_results')
parser.add_argument('--start_index', type=int, default=0)
parser.add_argument('--end_index', type=int, default=99)
args = parser.parse_args()
logger = misc.get_logger('sampling')
# Load config
config = misc.load_config(args.config)
train_config = misc.load_config(args.train_config)
logger.info(config)
misc.seed_all(config.sample.seed)
# Load checkpoint
ckpt = torch.load(config.model.checkpoint, map_location=args.device)
logger.info(f"Training Config: {train_config}")
# Transforms
protein_featurizer = trans.FeaturizeProteinAtom()
ligand_atom_mode = train_config.data.transform.ligand_atom_mode
ligand_featurizer = trans.FeaturizeLigandAtom(ligand_atom_mode)
transform = Compose([
protein_featurizer,
ligand_featurizer,
trans.FeaturizeLigandBond(),
])
# Load dataset
dataset, subsets = get_dataset(
config=train_config.data,
transform=transform
)
train_set, test_set = subsets['train'], subsets['test']
logger.info(f'Successfully load the dataset (size: {len(test_set)})!')
# Load model
model = ScorePosNet3D(
train_config.model,
protein_atom_feature_dim=protein_featurizer.feature_dim,
ligand_atom_feature_dim=ligand_featurizer.feature_dim
).to(args.device)
model.load_state_dict(ckpt['model'])
net_cond = BAPNet(ckpt_path=train_config.net_cond.ckpt_path, hidden_nf=train_config.net_cond.hidden_dim).to(args.device)
logger.info(f'Successfully load the model! {config.model.checkpoint}')
for data_id in range(args.start_index, args.end_index + 1):
data = test_set[data_id]
pred_pos, pred_v, pred_pos_traj, pred_v_traj, pred_v0_traj, pred_vt_traj, time_list = sample_diffusion_ligand(
model, data, config.sample.num_samples,
batch_size=args.batch_size, device=args.device,
num_steps=config.sample.num_steps,
pos_only=config.sample.pos_only,
center_pos_mode=config.sample.center_pos_mode,
sample_num_atoms=config.sample.sample_num_atoms,
net_cond=net_cond,
cond_dim=train_config.model.cond_dim
)
result = {
'data': data,
'pred_ligand_pos': pred_pos,
'pred_ligand_v': pred_v,
'pred_ligand_pos_traj': pred_pos_traj,
'pred_ligand_v_traj': pred_v_traj,
'time': time_list
}
logger.info('Sample done!')
print('sampled data_id: ', data_id)
result_path = args.result_path
os.makedirs(result_path, exist_ok=True)
shutil.copyfile(args.config, os.path.join(result_path, 'sample.yml'))
torch.save(result, os.path.join(result_path, f'result_{data_id}.pt'))