def __init__(self,
dataset: ScaffoldMolDataset,
sampler: ScaffoldMolSampler,
k: int = 5,
p: float = 0.5,
num_workers: int = 0,
ms=MoleculeSpec.get_default()):
"""
Construct ScaffoldLoader from the given dataset
Args:
dataset (Dataset):
The Dataset to be loaded
sampler (BatchSampler):
The batch sampler
k (int):
Number of importance samples, default to 5
p (float):
Degree of uncertainty during route sampling,
should be in (0, 1), default to 0.5
"""
self.k = k
# pylint: disable=invalid-name
self.p = p
# pylint: disable=invalid-name
self.ms = ms
super(DataLoader, self).__init__(dataset,
collate_fn=self._collate_fn,
batch_sampler=sampler,
num_workers=num_workers)
def _sample_ordering(mol, scaffold_nodes, k, p, ms=MoleculeSpec.get_default()):
"""Sampling decoding routes of a given molecule `mol`
Args:
mol (Chem.Mol): the given molecule (type: Chem.Mol)
scaffold_nodes (np.ndarray): the nodes marked as scaffold
k (int): The number of importance samples
p (float): Degree of uncertainty during route sampling, should be in (0, 1)
ms (mol_spec.MoleculeSpec)
Returns:
route_list (np.ndarray): route_list[i][j] the index of the atom reached at step j in sample i
step_ids_list (np.ndarray): step_ids_list[i][j] the step at which atom j is reach at sample i
logp_list (np.ndarray): logp_list[i] - the log-likelihood value of route i
"""
# build graph
atom_types = []
for atom in mol.GetAtoms():
atom_types.append(ms.get_atom_type(atom))
atom_ranks = []
for r in Chem.CanonicalRankAtoms(mol):
atom_ranks.append(r)
atom_ranks = np.array(atom_ranks)
bonds = []
for b in mol.GetBonds():
idx_1, idx_2 = b.GetBeginAtomIdx(), b.GetEndAtomIdx()
bonds.append([idx_1, idx_2])
# build nx graph
graph = nx.Graph()
graph.add_nodes_from(range(len(atom_ranks)))
graph.add_edges_from(bonds)
route_list = []
step_ids_list = []
logp_list = []
for _ in range(k):
step_ids, log_p = _traverse(graph=graph, atom_ranks=atom_ranks, scaffold_nodes=scaffold_nodes, p=p)
step_ids_list.append(step_ids)
step_ids = np.argsort(step_ids)
route_list.append(step_ids)
logp_list.append(log_p)
# cast to numpy array
route_list = np.array(route_list, dtype=np.int32)
step_ids_list = np.array(step_ids_list, dtype=np.int32)
logp_list = np.array(logp_list, dtype=np.float32)
return route_list, step_ids_list, logp_list
def get_data_loader_full(scaffold_network_loc: str,
molecule_smiles_loc: str,
batch_size: int,
num_iterations: int,
num_workers: int,
k: int,
p: float,
ms: MoleculeSpec = MoleculeSpec.get_default()
) -> DataLoader:
"""Helper function for getting the dataloader
Args:
scaffold_network_loc (str):
The location to the network file
molecule_smiles_loc (str):
The location to the file containing molecular SMILES
batch_size (int):
Batch size for training
num_iterations (int):
The number of iterations to train
num_workers (int):
The number of workers used for data loading
k (int)
p (float)
ms (MoleculeSpec, optional)
Returns:
t.Tuple[DataLoader, DataLoader]:
The loader for training data and test data
"""
# Get dataset
# pylint: disable=invalid-name
db = ScaffoldMolDataset(scaffold_network_loc, molecule_smiles_loc)
# batch_size
assert batch_size % 2 == 0
# Get sampler
sampler = ScaffoldMolSampler(db,
(batch_size // 2, batch_size // 2),
num_iterations,
None, None, None)
# Get DataLoaders
loader = DataLoader(db, sampler, k, p, num_workers, ms)
return loader
def get_data_loader_full(scaffold_network_loc,
molecule_smiles_loc,
batch_size,
num_iterations,
num_workers,
k,
p,
ms=MoleculeSpec.get_default()):
"""Helper function for getting the dataloader
Args:
scaffold_network_loc (str): The location to the network file
molecule_smiles_loc (str): The location to the file containing molecular SMILES
batch_size (int): Batch size for training
num_iterations (int): The number of iterations to train
num_workers (int): The number of workers used for data loading
k (int)
p (float)
ms (MoleculeSpec, optional)
Returns:
t.Tuple[DataLoader, DataLoader]: The loader for training data and test data
"""
# Get dataset
db = ScaffoldMolDataset(scaffold_network_loc=scaffold_network_loc,
molecule_smiles_loc=molecule_smiles_loc)
# batch_size
assert batch_size % 2 == 0
# Get sampler
sampler = ScaffoldMolSampler(dataset=db,
batch_size=(batch_size // 2, batch_size // 2),
num_iterations=num_iterations,
exclude_ids_loc=None,
training=None,
split_type=None)
# Get DataLoaders
loader = DataLoader(db, sampler, k, p, num_workers, ms)
return loader
def pack_encoder(
mol_array, ms=MoleculeSpec.get_default()) -> t.Tuple[torch.Tensor]:
"""
Pack and expand information in mol_array in order to feed into graph
encoders (The encoder version of the function `pack()`)
Args:
mol_array (torch.Tensor):
input molecule array
size [batch_size, max_num_steps, 5], type: `torch.long`
where 5 = atom_type + begin_ids + end_ids + bond_type
ms (mol_spec.MoleculeSpec)
Returns:
atom_types (torch.Tensor):
Atom type information packed into a single vector, type: torch.long
is_scaffold (torch.Tensor):
Whether the corresponding atom is contained in the scaffold,
type: torch.long
bond_info (torch.Tensor):
Bond type information packed into a single matrix
type: torch.long, shape: [-1, 3],
3 = begin_ids + end_ids + bond_type
block_ids, atom_ids (torch.Tensor):
type: torch.long, shape: [num_total_atoms, ]
"""
# get device info
device = mol_array.device
# magical numbers
I_ATOM_TYPE, I_BEGIN_IDS, I_END_IDS, I_BOND_TYPE, I_IS_SCAFFOLD = range(5)
# The number of decoding steps required for each input molecule
# size: [batch_size, ]
num_steps = mol_array[:, :, I_END_IDS].ge(0).long().sum(-1)
# Get molecule id and step id for each (unexpanded) atom/node
# Example:
# if we have num_steps = [4, 2, 5] and batch_size = 3, then
# molecule: | 0 | 1 | 2 |
# mol_ids = [0 0 0 0 1 1 2 2 2 2 2]
# step_ids = [0 1 2 3 0 1 0 1 2 3 4]
mol_ids, step_ids = rep_and_range(num_steps)
mol_array_packed = mol_array[mol_ids, step_ids, :]
# Get the expanded atom type
atom_types, is_scaffold = (mol_array_packed[:, I_ATOM_TYPE],
mol_array_packed[:, I_IS_SCAFFOLD])
# binary vector with int values
is_connect = atom_types.ge(0).long()
is_connect_index = is_connect.nonzero().squeeze()
num_atoms = torch_scatter.scatter_add(is_connect, dim=0, index=mol_ids)
atom_types = atom_types[is_connect_index]
is_scaffold = is_scaffold[is_connect_index]
block_ids, atom_ids = rep_and_range(num_atoms)
# Get last append mask
# Locations of the latest appended atoms
last_append_loc = torch.cumsum(num_atoms, dim=0) - 1
# Initialize last_append_mask as zeros
last_append_mask = torch.full_like(is_scaffold, 0)
# Fill the latest appended atoms as one
last_append_mask[last_append_loc] = 1
# Get (packed) bond information
# size: [-1, 3], where 3=begin_ids, end_ids, bond_type
bond_info = mol_array_packed[:, [I_BEGIN_IDS, I_END_IDS, I_BOND_TYPE]]
# adjust begin_ids and end_ids for each bond
num_atoms_cumsum = pad_first(torch.cumsum(num_atoms, dim=0)[:-1])
I_BOND_BEGIN_IDS = 0
_filter = bond_info[:, I_BOND_BEGIN_IDS].ge(0).nonzero().squeeze()
_shift = num_atoms_cumsum[mol_ids]
_shift = torch.stack([
_shift,
] * 2 + [torch.zeros_like(_shift)], dim=1)
bond_info = (bond_info + _shift)[_filter, :]
# symmetrize bond_info
bond_info = torch.cat([bond_info, bond_info[:, [1, 0, 2]]], )
# labels for artificial bonds and atoms
(I_BOND_REMOTE_2, I_BOND_REMOTE_3,
I_BOND_ATOM_SELF) = range(ms.num_bond_types, ms.num_bond_types + 3)
# artificial bond type: remote connection
indices = bond_info[:, :2].cpu().numpy()
size = atom_types.size(0)
d_indices_2, d_indices_3 = get_remote_connection(indices, size)
# pylint: disable=not-callable
d_indices_2, d_indices_3 = (torch.tensor(d_indices_2,
dtype=torch.long,
device=device),
torch.tensor(d_indices_3,
dtype=torch.long,
device=device))
bond_type = torch.full([d_indices_2.size(0), 1],
I_BOND_REMOTE_2,
dtype=torch.long,
device=device)
bond_info_remote_2 = torch.cat([d_indices_2, bond_type], dim=-1)
bond_type = torch.full([d_indices_3.size(0), 1],
I_BOND_REMOTE_3,
dtype=torch.long,
device=device)
bond_info_remote_3 = torch.cat([d_indices_3, bond_type], dim=-1)
bond_info = torch.cat([bond_info, bond_info_remote_2, bond_info_remote_3],
dim=0)
# artificial bond type: self connection
begin_ids = end_ids = torch.arange(atom_types.size(0),
dtype=torch.long,
device=atom_types.device)
bond_type = torch.full_like(end_ids, I_BOND_ATOM_SELF)
bond_info_self = torch.stack([begin_ids, end_ids, bond_type], dim=-1)
bond_info = torch.cat([bond_info, bond_info_self], dim=0)
return (atom_types, is_scaffold, bond_info, last_append_mask, block_ids,
atom_ids)
def pack_decoder(
mol_array: torch.Tensor, ms=MoleculeSpec.get_default()
) -> t.Tuple[torch.Tensor, ...]:
"""
Pack and expand information in mol_array in order to feed into the neural
network
Args:
mol_array (torch.Tensor):
input molecule array,
size [batch_size, max_num_steps, 5], type: `torch.long`
5 = atom_type + begin_ids + end_ids + bond_type + is_scaffold
ms (mol_spec.MoleculeSpec)
Returns:
atom_types (torch.Tensor):
Atom type information packed into a single vector, type: torch.long
is_scaffold (torch.Tensor):
Whether the corresponding atom is contained in the scaffold,
type: torch.long
bond_info (torch.Tensor):
Bond type information packed into a single matrix,
type: torch.long, shape: [-1, 3]
3 = begin_ids + end_ids + bond_type
actions (torch.Tensor):
The action to carry out at each step, type: torch.long, shape: [-1, 5]
5 = action_type + atom_type + bond_type + append_loc + connect_loc
mol_ids, step_ids, block_ids (torch.Tensor):
Index information, type: torch.long
"""
# get device info
device = mol_array.device
# magic numbers
I_ATOM_TYPE, I_BEGIN_IDS, I_END_IDS, I_BOND_TYPE, I_IS_SCAFFOLD = range(5)
# The number of decoding steps required for the entire molecule
# size: [batch_size, ]
num_total_steps = mol_array[:, :, I_END_IDS].ge(0).long().sum(-1)
# The number of steps required for the generation of scaffold,
# size: [batch_size, ]
num_scaffold_steps = mol_array[:, :, I_IS_SCAFFOLD].eq(1).long().sum(-1)
# The number of steps required for the generation of side chains,
# size: [batch_size, ]
# NOTE: The additional 1 step is the termination step
num_steps = num_total_steps - num_scaffold_steps + 1
# Get molecule id and step id for each (unexpanded) atom/node
# Example:
# if we have num_steps = [4, 2, 5] and batch_size = 3, then
# molecule: | 0 | 1 | 2 |
# mol_ids = [0 0 0 0 1 1 2 2 2 2 2]
# step_ids = [0 1 2 3 0 1 0 1 2 3 4]
mol_ids, step_ids = rep_and_range(num_steps)
# Expanding molecule
# Example:
# if we have num_steps = [3, 2],
# batch_size = 2,
# step_ids = [0 1 2 0 1]
# and num_scaffold_steps=[3, 2], then
# molecule: | 0 | 1 |
# num_steps: | 3 | 2 |
# steps: | 0 | 1 | 2 | 0 | 1 |
# rep_ids_rep = [0 0 0 1 1 1 1 2 2 2 2 2 3 3 4 4 4]
# indexer = [0 1 2 0 1 2 3 0 1 2 3 4 0 1 0 1 2]
(rep_ids_rep,
indexer) = rep_and_range(step_ids + num_scaffold_steps[mol_ids])
# Expanding mol_ids
# Example:
# molecule: | 0 | 1 |
# mol_ids: | 0 | 0 | 0 | 1 | 1 |
# rep_ids_rep = [0 0 0 1 1 1 1 2 2 2 2 2 3 3 4 4 4]
# mol_ids_rep = [0 0 0 0 0 0 0 0 0 0 0 0 1 1 1 1 1]
mol_ids_rep = mol_ids[rep_ids_rep]
# Expanding and packing mol_array
# Example:
# if we have
# mol_array = a1 a2 a3 a4 a5
# b1 b2 b3 -- --
# where: a1 = [atom_type, begin_ids, end_ids, bond_type is_scaffold]
# -- = [-1 -1 -1 -1 -1 ]
# then
# indexer = [0 1 2 0 1 2 3 0 1 2 3 4 0 1 0 1 2 ]
# mol_ids_rep = [0 0 0 0 0 0 0 0 0 0 0 0 1 1 1 1 1 ]
# mol_array_packed = [a1 a2 a3 a1 a2 a3 a4 a1 a2 a3 a4 a5 b1 b2 b1 b2 b3]
# shape: [-1, 4]
mol_array_packed = mol_array[mol_ids_rep, indexer, :]
# Get the expanded atom type
atom_types, is_scaffold = (mol_array_packed[:, I_ATOM_TYPE],
mol_array_packed[:, I_IS_SCAFFOLD])
# Get the number of atom at each step: |V_i|
# Example:
# molecule: | 0 | 1 |
# steps: | 0 | 1 | 2 | 0 | 1 |
# num_atoms = [ 3 , 4 , 5 , 2 , 3 ]
# Note: connect actions should be first filtered
# binary vector with int values
is_connect = atom_types.ge(0).long()
is_connect_index = is_connect.nonzero().squeeze()
num_atoms = torch_scatter.scatter_add(is_connect, dim=0, index=rep_ids_rep)
atom_types = atom_types[is_connect_index]
is_scaffold = is_scaffold[is_connect_index]
# Get last_append_mask
OLD_ATOM, NEW_APPEND, NEW_CONNECT = range(3)
# Locations of the latest appended atoms
last_append_loc = torch.cumsum(num_atoms, dim=0) - 1
# Initialize last_append_mask as zeros
last_append_mask = torch.full_like(is_scaffold, OLD_ATOM)
last_append_mask[last_append_loc] = torch.where(
is_scaffold[last_append_loc].eq(1),
torch.full_like(last_append_loc, OLD_ATOM),
torch.where(num_atoms.gt(pad_first(num_atoms[:-1])),
torch.full_like(last_append_loc, NEW_APPEND),
torch.full_like(last_append_loc, NEW_CONNECT)))
# block_ids, essentially equal to the filtered rep_ids_rep
block_ids, atom_ids = rep_and_range(num_atoms)
# Get (packed) bond information
# size: [-1, 3], where 3=begin_ids, end_ids, bond_type
bond_info = mol_array_packed[:, [I_BEGIN_IDS, I_END_IDS, I_BOND_TYPE]]
# adjust begin_ids and end_ids for each bond
num_atoms_cumsum = pad_first(torch.cumsum(num_atoms, dim=0)[:-1])
I_BOND_BEGIN_IDS = 0
_filter = bond_info[:, I_BOND_BEGIN_IDS].ge(0).nonzero().squeeze()
_shift = num_atoms_cumsum[rep_ids_rep]
_shift = torch.stack([
_shift,
] * 2 + [torch.zeros_like(_shift)], dim=1)
bond_info = (bond_info + _shift)[_filter, :]
# symmetrize bond_info
bond_info = torch.cat([bond_info, bond_info[:, [1, 0, 2]]], )
# labels for artificial bonds
(I_BOND_REMOTE_2, I_BOND_REMOTE_3,
I_BOND_ATOM_SELF) = range(ms.num_bond_types, ms.num_bond_types + 3)
# artificial bond type: remote connection
indices = bond_info[:, :2].cpu().numpy()
size = atom_types.size(0)
d_indices_2, d_indices_3 = get_remote_connection(indices, size)
# pylint: disable=not-callable
d_indices_2, d_indices_3 = (torch.tensor(d_indices_2,
dtype=torch.long,
device=device),
torch.tensor(d_indices_3,
dtype=torch.long,
device=device))
bond_type = torch.full([d_indices_2.size(0), 1],
I_BOND_REMOTE_2,
dtype=torch.long,
device=device)
bond_info_remote_2 = torch.cat([d_indices_2, bond_type], dim=-1)
bond_type = torch.full([d_indices_3.size(0), 1],
I_BOND_REMOTE_3,
dtype=torch.long,
device=device)
bond_info_remote_3 = torch.cat([d_indices_3, bond_type], dim=-1)
bond_info = torch.cat([bond_info, bond_info_remote_2, bond_info_remote_3],
dim=0)
# artificial bond type: self connection
begin_ids = end_ids = torch.arange(atom_types.size(0),
dtype=torch.long,
device=atom_types.device)
bond_type = torch.full_like(end_ids, I_BOND_ATOM_SELF)
bond_info_self = torch.stack([begin_ids, end_ids, bond_type], dim=-1)
bond_info = torch.cat([bond_info, bond_info_self], dim=0)
# compile action for each step, which contains the following information
# 1. the type of action to carry out: append, connect or terminate
# 2. the type of atom to append (0 for connect and termination actions)
# 3. the type of bond to connect (0 for termination actions)
# 4. the location to append (0 for connect and termination actions)
# 5. the location to connect (0 for append and termination actions)
# get the batch size
batch_size = mol_array.size(0)
padding = torch.full([batch_size, 1, 5],
-1,
dtype=torch.long,
device=torch.device('cuda:0'))
actions = torch.cat([mol_array, padding], dim=1)
actions = actions[mol_ids, step_ids + num_scaffold_steps[mol_ids], :]
# 1. THE TYPE OF ACTION PERFORMED AT EACH STEP
# 0 for append, 1 for connect, 2 for termination
I_MASK, I_APPEND, I_CONNECT, I_END = 0, 0, 1, 2
def _full(_x):
"""A helper class to create a constant matrix
with the same type and length as actions with a given content"""
return torch.full([
actions.size(0),
],
_x,
dtype=torch.long,
device=mol_array.device)
action_type = torch.where(
# if the atom type is defined for step i
actions[:, I_ATOM_TYPE].ge(I_MASK),
# the the action type is set to 'append'
_full(I_APPEND),
torch.where(
# if the bond type is defined for step i
actions[:, I_BOND_TYPE].ge(I_MASK),
# then the action is set to 'connect'
_full(I_CONNECT),
# else 'terminate'
_full(I_END)))
# 2. THE TYPE OF ATOM ADDED AT EACH 'APPEND' STEP
action_atom_type = torch.where(actions[:, I_ATOM_TYPE].ge(I_MASK),
actions[:, I_ATOM_TYPE], _full(I_MASK))
# 3. THE BOND TYPE AT EACH STEP
action_bond_type = torch.where(actions[:, I_BOND_TYPE].ge(0),
actions[:, I_BOND_TYPE], _full(I_MASK))
# 4. THE LOCATION TO APPEND AT EACH STEP
append_loc = torch.where(action_type.eq(0),
actions[:, I_BEGIN_IDS] + num_atoms_cumsum,
_full(I_MASK))
# 5. THE LOCATION TO CONNECT AT EACH STEP
connect_loc = torch.where(action_type.eq(1),
actions[:, I_END_IDS] + num_atoms_cumsum,
_full(I_MASK))
# Stack everything together
# size: [-1, 5]
# 5 = action_type, atom_type, bond_type, append_loc, connect_loc
actions = torch.stack([
action_type, action_atom_type, action_bond_type, append_loc,
connect_loc
],
dim=-1)
return (
# 1. structure information:
# atom (node) type and bond (edge) information
atom_types,
is_scaffold,
bond_info,
last_append_mask,
# 2. action to carry out at each step
actions,
# 3. indices
mol_ids,
step_ids,
block_ids,
atom_ids)
from itertools import chain
import numpy as np
import networkx as nx
from rdkit import Chem
from rdkit.Chem import rdmolops
from scipy import sparse
from mol_spec import MoleculeSpec
__all__ = [
# "smiles_to_nx_graph",
"WeaveMol",
]
ms = MoleculeSpec.get_default()
class WeaveMol(object):
def __init__(self, smiles: str):
self.smiles = smiles
self.mol = Chem.MolFromSmiles(smiles)
self.ms = ms
self.num_atom_types = ms.num_atom_types
self.num_bond_types = ms.num_bond_types
self.num_atoms = self.mol.GetNumAtoms()
self.original_atoms = list(range(self.num_atoms))
self.num_original_bonds = self.mol.GetNumBonds()
self._atom_types = None
self._original_bond_info = None
self._original_bond_info_np = None
def get_data_loader(scaffold_network_loc,
molecule_smiles_loc,
exclude_ids_loc,
split_type,
batch_size,
batch_size_test,
num_iterations,
num_workers,
k,
p,
ms=MoleculeSpec.get_default()):
"""Helper function for getting the dataloader
Args:
scaffold_network_loc (str): The location to the network file
molecule_smiles_loc (str): The location to the file containing molecular SMILES
exclude_ids_loc (str): File storing the indices of which molecule/scaffold should be excluded
split_type (str): The type of split, should be 'scaffold' or 'molecule'
batch_size (int): Batch size for training
batch_size_test (int): Batch size for test
num_iterations (int): The number of iterations to train
num_workers (int): The number of workers used for data loading
k (int)
p (float)
ms (MoleculeSpec, optional)
Returns:
t.Tuple[DataLoader, DataLoader]: The loader for training data and test data
"""
# Get dataset
db = ScaffoldMolDataset(scaffold_network_loc, molecule_smiles_loc)
assert batch_size % 2 == 0 and batch_size_test % 2 == 0
sampler_train = ScaffoldMolSampler(dataset=db,
batch_size=(batch_size // 2,
batch_size // 2),
num_iterations=num_iterations,
exclude_ids_loc=exclude_ids_loc,
training=True,
split_type=split_type)
sampler_test = ScaffoldMolSampler(dataset=db,
batch_size=(batch_size_test // 2,
batch_size_test // 2),
num_iterations=num_iterations,
exclude_ids_loc=exclude_ids_loc,
training=False,
split_type=split_type)
# Get DataLoaders
loader_train = DataLoader(dataset=db,
sampler=sampler_train,
k=k,
p=p,
num_workers=num_workers,
ms=ms)
loader_test = DataLoader(dataset=db,
sampler=sampler_test,
k=k,
p=p,
num_workers=0,
ms=ms)
return loader_train, loader_test
def engine(ckpt_loc='ckpt/ckpt-default',
molecule_loc='data_utils/molecules.smi',
network_loc='data_utils/scaffolds_molecules.pkl.gz',
exclude_ids_loc='ckpt/ckpt-default/exclude_ids.txt',
full=False,
split_by='molecule',
training_only=False,
num_workers=2,
num_atom_embedding=16,
causal_hidden_sizes=(32, 64),
num_bn_features=96,
num_k_features=24,
num_layers=20,
num_output_features=256,
efficient=False,
ms=MoleculeSpec.get_default(),
activation='elu',
lr=1e-3,
decay=0.01,
decay_step=100,
min_lr=5e-5,
summary_step=200,
clip_grad=3.0,
batch_size=128,
batch_size_test=256,
num_iterations=50000,
k=5,
p=0.5,
gpu_ids=(0, 1, 2, 3)):
"""Engine for training scaffold based VAE
Args:
ckpt_loc (str): Location to store model checkpoints
molecule_loc (str): Location of molecule SMILES strings
network_loc (str): Location of the bipartite network
exclude_ids_loc (str): The location storing the ids to be excluded from the training set
full (bool): Whether to use the full dataset for training, default to False
split_by (str): Whether to split by scaffold or molecule
training_only (str): Recording only training loss, default to False
num_workers (int): Number of workers used during data loading, default to 1
num_atom_embedding (int): The size of the initial node embedding
causal_hidden_sizes (tuple[int] or list[int]): The size of hidden layers in causal weave blocks
num_bn_features (int): The number of features used in bottleneck layers in each dense layer
num_k_features (int): The growth rate of dense net
num_layers (int): The number of densenet layers
num_output_features (int): The number of output features for the densenet
efficient (bool): Whether to use the memory efficient implementation of densenet
ms (mol_spec.MoleculeSpec)
activation (str): The activation function used, default to 'elu'
lr (float): (Initial) learning rate
decay (float): The rate of learning rate decay
decay_step (int): The interval of each learning rate decay
min_lr (float): The minimum learning rate
summary_step (int): Interval of summary
clip_grad (float): Gradient clipping
batch_size (int): The batch size for training
batch_size_test (int): The batch size for testing
num_iterations (int): The number of total iterations for model training
k (int): The number of importance samples
p (float): The degree of stochasticity of importance sampling 0.0 for fully stochastic decoding, 1.0 for fully
deterministic decoding
gpu_ids (tuple[int] or list[int]): Which GPUs are used for training
"""
# ANCHOR Check whether to continue training
is_continuous = _check_continuous(ckpt_loc)
# ANCHOR Create iterators for training and test dataset
loader_train, loader_test = _get_loader(network_loc=network_loc,
molecule_loc=molecule_loc,
exclude_ids_loc=exclude_ids_loc,
split_by=split_by,
batch_size=batch_size,
batch_size_test=batch_size_test,
num_iterations=num_iterations,
num_workers=num_workers,
full=full,
training_only=training_only,
k=k,
p=p,
ms=ms)
iter_train = iter(loader_train)
iter_test = iter(loader_test) if loader_test is not None else None
# ANCHOR Initialize model with random params
mdl = _init_mdl(num_atom_embedding=num_atom_embedding,
causal_hidden_sizes=causal_hidden_sizes,
num_bn_features=num_bn_features,
num_k_features=num_k_features,
num_layers=num_layers,
num_output_features=num_output_features,
efficient=efficient,
activation=activation,
gpu_ids=gpu_ids)
# ANCHOR Initialize optimizer and scheduler
optimizer = optim.Adam(mdl.parameters(), lr=lr)
scheduler = optim.lr_scheduler.StepLR(optimizer, decay_step, 1.0 - decay)
# ANCHOR Load previously stored states
if is_continuous:
# restore states
mdl, optimizer, scheduler, t0, global_counter = _restore(
mdl=mdl,
optimizer=optimizer,
scheduler=scheduler,
ckpt_loc=ckpt_loc)
else:
t0 = time.time()
global_counter = 0
device = torch.device(f'cuda:{gpu_ids[0]}')
with open(os.path.join(ckpt_loc, 'log.out'),
mode='a' if is_continuous else 'w') as f:
if not is_continuous:
f.write('global_step\ttime(min)\tloss\tlr\n')
try:
while True:
global_counter += 1 # Update global counter
# Perform one-step of training
loss = _train_step(mdl=mdl,
optimizer=optimizer,
scheduler=scheduler,
min_lr=min_lr,
clip_grad=clip_grad,
device=device,
iter_train=iter_train)
if global_counter % summary_step == 0:
if not training_only:
try:
loss = _test_step(mdl, device, iter_test)
except StopIteration:
iter_test = iter(loader_test)
loss = _test_step(mdl, device, iter_test)
loss = loss.item()
# Get learning rate
current_lr = [
params_group['lr']
for params_group in optimizer.param_groups
][0]
# Save status
message_str = _save(mdl=mdl,
optimizer=optimizer,
scheduler=scheduler,
global_counter=global_counter,
t0=t0,
loss=loss,
current_lr=current_lr,
ckpt_loc=ckpt_loc)
f.write(message_str)
f.flush()
except StopIteration:
if not training_only:
try:
loss = _test_step(mdl, device, iter_test)
except StopIteration:
iter_test = iter(loader_test)
loss = _test_step(mdl, device, iter_test)
loss = loss.item()
# Get learning rate
current_lr = [
params_group['lr'] for params_group in optimizer.param_groups
][0]
# Save status
message_str = _save(mdl=mdl,
optimizer=optimizer,
scheduler=scheduler,
global_counter=global_counter,
t0=t0,
loss=loss,
current_lr=current_lr,
ckpt_loc=ckpt_loc)
f.write(message_str)
f.flush()
f.write('Training finished')
def __init__(self,
num_atom_embedding: int,
causal_hidden_sizes: int,
num_bn_features: int,
num_k_features: int,
num_layers: int,
num_output_features: int,
efficient: bool = False,
ms: MoleculeSpec = MoleculeSpec.get_default(),
activation: str = 'elu',
conditional: bool = False,
num_cond_features: t.Optional[int] = None,
activation_cond: t.Optional[str] = None):
"""
The constructor
Args:
num_atom_embedding (int):
The size of the initial node embedding
causal_hidden_sizes (tuple[int]):
The size of hidden layers in causal weave blocks
num_bn_features (int):
The number of features used in bottleneck layers in each dense
layer
num_k_features (int):
The growth rate of dense net
num_layers (int):
The number of densenet layers
num_output_features (int):
The number of output features for the densenet
efficient (bool):
Whether to use the memory efficient BNReLULinearimplementation
of densenet
ms (mol_spec.MoleculeSpec)
activation (str):
The activation function used, default to 'elu'
conditional (bool):
Whether to include conditional input, default to False
num_cond_features (int or None):
The size of conditional input, should be None if
self.conditional is False
activation_cond (str or None):
Activation function used for conditional input
should be None if self.conditional is False
"""
super(DeepScaffold, self).__init__()
self.num_atom_embedding = num_atom_embedding
self.causal_hidden_sizes = causal_hidden_sizes
self.num_bn_features = num_bn_features
self.num_k_features = num_k_features
self.num_layers = num_layers
self.num_output_features = num_output_features
self.efficient = efficient
# pylint: disable=invalid-name
self.ms = ms
# 3 = 2 * remote connection + self connection
self._num_bond_types = self.ms.num_bond_types + 3
self._num_atom_types = self.ms.num_atom_types
self.activation = activation
self.conditional = conditional
self.num_cond_features = num_cond_features
self.activation_cond = activation_cond
# embedding layer for atom types and bond types
# 3 = is_scaffold + new_append + new_connect
self.atom_embedding = nn.Embedding((self._num_atom_types +
self.ms.num_atom_types * 3),
self.num_atom_embedding)
# convolution layer
self.mol_conv = DenseNet(self.num_atom_embedding,
self._num_bond_types,
self.causal_hidden_sizes,
self.num_bn_features,
self.num_k_features,
self.num_layers,
self.num_output_features,
self.efficient,
self.activation,
self.conditional,
self.num_cond_features,
self.activation_cond)
# Pooling layer
self.avg_pool = AvgPooling(self.num_output_features,
self.activation)
# output layers
self.end = BNReLULinear(self.num_output_features,
1,
self.activation)
self.append_connect = \
BNReLULinear(self.num_output_features * 2,
ms.num_atom_types * ms.num_bond_types +
ms.num_bond_types,
self.activation)
def get_mol_from_array(mol_array, sanitize=True, ms=MoleculeSpec.get_default()):
"""Converting molecule array to Chem.Mol objects
Args:
mol_array (np.ndarray): The array representation of molecules
dtype: int, shape: [num_samples, num_steps, 5]
sanitize (bool): Whether to sanitize the output molecule, default to True
ms (mol_spec.MoleculeSpec)
Returns:
list[Chem.Mol]: mol_list - The list of output molecules
"""
# shape: num_samples, num_steps
is_scaffold = mol_array[:, :, -1]
# shape: num_samples, num_steps, 5
mol_array = mol_array[:, :, :-1]
# get shape information
num_samples, max_num_steps, _ = mol_array.shape
# initialize the list of output molecules
mol_list = []
# loop over molecules
for mol_id in range(num_samples):
try:
mol = Chem.RWMol(Chem.Mol()) # initialize molecule
atom_list = [] # List to store all created atoms
scaffold_atoms = [] # List to store all scaffold atoms
aromatic_atoms = [] # List to store all aromatic atoms
n_atoms = [] # The indices of all nitrogen atoms
for step_id in range(max_num_steps):
atom_type, begin_ids, end_ids, bond_type = mol_array[mol_id, step_id, :].tolist()
if end_ids == -1:
# if the actions is to terminate
break
elif begin_ids == -1:
# if the action is to initialize
new_atom = ms.index_to_atom(atom_type)
mol.AddAtom(new_atom)
atom_list.append(new_atom)
if new_atom.GetSymbol() == 'N':
n_atoms.append(end_ids)
elif atom_type == -1:
# if the action is to connect
ms.index_to_bond(mol, begin_ids, end_ids, bond_type)
else:
# if the action is to append new atom
new_atom = ms.index_to_atom(atom_type)
mol.AddAtom(new_atom)
ms.index_to_bond(mol, begin_ids, end_ids, bond_type)
# Record atom
atom_list.append(new_atom)
if is_scaffold[mol_id, step_id]:
# Both ends are scaffold atoms
scaffold_atoms.append(end_ids)
scaffold_atoms.append(begin_ids)
if bond_type == ms.bond_orders.index(Chem.BondType.AROMATIC):
aromatic_atoms.append(begin_ids)
aromatic_atoms.append(end_ids)
if new_atom.GetSymbol() == 'N':
n_atoms.append(end_ids)
special_atoms = (set(scaffold_atoms) & set(aromatic_atoms) & set(n_atoms))
scaffold_atoms = set(scaffold_atoms)
for atom_id in special_atoms:
neighbors = (mol_array[mol_id, mol_array[mol_id, :, 2] == atom_id, 1].tolist() +
mol_array[mol_id, mol_array[mol_id, :, 1] == atom_id, 2].tolist())
neighbors = set(neighbors) - {-1}
if neighbors - scaffold_atoms:
atom_i = mol.GetAtomWithIdx(atom_id)
if atom_i.GetNumExplicitHs() > 0:
num_explict_hs = atom_i.GetNumExplicitHs() - 1
atom_i.SetNumExplicitHs(num_explict_hs)
else:
num_formal_charge = atom_i.GetFormalCharge() + 1
atom_i.SetFormalCharge(num_formal_charge)
if sanitize:
mol = mol.GetMol()
Chem.SanitizeMol(mol)
except (ValueError, RuntimeError):
mol = None
mol_list.append(mol)
return mol_list
def get_array_from_mol(mol, scaffold_nodes, nh_nodes, np_nodes, k, p, ms=MoleculeSpec.get_default()):
"""Represent the molecule using `np.ndarray`
Args:
mol (Chem.Mol): The input molecule
scaffold_nodes (Iterable): The location of scaffold represented as `list`/`np.ndarray`
nh_nodes (Iterable): Nodes with modifications
np_nodes (Iterable): Nodes with modifications
k (int): The number of importance samples
p (float): Degree of uncertainty during route sampling, should be in (0, 1)
ms (mol_spec.MoleculeSpec)
Returns:
mol_array (np.ndarray): The numpy representation of the molecule
dtype - np.int32, shape - [k, num_bonds + 1, 5]
logp (np.ndarray): The log-likelihood of each route
dtype - np.float32, shape - [k, ]
"""
atom_types = []
bond_info = []
num_bonds = mol.GetNumBonds()
# sample route
scaffold_nodes = np.array(list(scaffold_nodes), dtype=np.int32)
route_list, step_ids_list, logp = _sample_ordering(mol=mol, scaffold_nodes=scaffold_nodes, k=k, p=p)
for atom_id, atom in enumerate(mol.GetAtoms()):
if atom_id in nh_nodes:
atom.SetNumExplicitHs(atom.GetNumExplicitHs() + 1)
if atom_id in np_nodes:
atom.SetFormalCharge(atom.GetFormalCharge() - 1)
atom_types.append(ms.get_atom_type(atom))
for bond in mol.GetBonds():
bond_info.append([bond.GetBeginAtomIdx(), bond.GetEndAtomIdx(), ms.get_bond_type(bond)])
# shape:
# atom_types: num_atoms
# bond_info: num_bonds x 3
atom_types = np.array(atom_types, dtype=np.int32)
bond_info = np.array(bond_info, dtype=np.int32)
# initialize packed molecule array data
mol_array = []
for sample_id in range(k):
# get the route and step_ids for the i-th sample
route_i = route_list[sample_id, :]
step_ids_i = step_ids_list[sample_id, :]
# reorder atom types and bond info
# note: bond_info [start_ids, end_ids, bond_type]
atom_types_i, bond_info_i, is_append = _reorder(atom_types=atom_types, bond_info=bond_info, route=route_i,
step_ids=step_ids_i)
# atom type added at each step
# -1 if the current step is connect
atom_types_added = np.full([num_bonds, ], -1, dtype=np.int32)
atom_types_added[is_append] = atom_types_i[bond_info_i[:, 1]][is_append]
# pack into mol_array_i
# size: num_bonds x 4
# note: [atom_types_added, start_ids, end_ids, bond_type]
mol_array_i = np.concatenate([atom_types_added[:, np.newaxis], bond_info_i], axis=-1)
# add initialization step
init_step = np.array([[atom_types_i[0], -1, 0, -1]], dtype=np.int32)
# concat into mol_array
# size: (num_bonds + 1) x 4
mol_array_i = np.concatenate([init_step, mol_array_i], axis=0)
# Mark up scaffold bonds
is_scaffold = np.logical_and(mol_array_i[:, 1] < len(scaffold_nodes), mol_array_i[:, 2] < len(scaffold_nodes))
is_scaffold = is_scaffold.astype(np.int32)
# Concatenate
# shape: k x (num_bonds + 1) x 5
mol_array_i = np.concatenate((mol_array_i, is_scaffold[:, np.newaxis]), axis=-1)
mol_array.append(mol_array_i)
# num_samples x (num_bonds + 1) x 4
mol_array = np.stack(mol_array, axis=0)
# Output size:
# mol_array: k x (num_bonds + 1) x 4
# logp: k
return mol_array, logp
def get_data_loader(scaffold_network_loc: str,
molecule_smiles_loc: str,
exclude_ids_loc: str,
split_type: str,
batch_size: int,
batch_size_test: int,
num_iterations: int,
num_workers: int,
k: int,
p: float,
ms: MoleculeSpec = MoleculeSpec.get_default()
) -> t.Tuple[DataLoader, DataLoader]:
"""Helper function for getting the dataloader
Args:
scaffold_network_loc (str):
The location to the network file
molecule_smiles_loc (str):
The location to the file containing molecular SMILES
exclude_ids_loc (str):
File storing the indices of which molecule/scaffold should
be excluded
split_type (str):
The type of split, should be 'scaffold' or 'molecule'
batch_size (int):
Batch size for training
batch_size_test (int):
Batch size for test
num_iterations (int):
The number of iterations to train
num_workers (int):
The number of workers used for data loading
k (int)
p (float)
ms (MoleculeSpec, optional)
Returns:
t.Tuple[DataLoader, DataLoader]:
The loader for training data and test data
"""
# Get dataset
# pylint: disable=invalid-name
db = ScaffoldMolDataset(scaffold_network_loc,
molecule_smiles_loc)
assert batch_size % 2 == 0 and batch_size_test % 2 == 0
(sampler_train,
sampler_test) = (ScaffoldMolSampler(db,
(batch_size // 2,
batch_size // 2),
num_iterations,
exclude_ids_loc,
True,
split_type),
ScaffoldMolSampler(db,
(batch_size_test // 2,
batch_size_test // 2),
num_iterations,
exclude_ids_loc,
False,
split_type))
# Get DataLoaders
loader_train, loader_test = \
(DataLoader(db, sampler_train, k, p, num_workers, ms),
DataLoader(db, sampler_test, k, p, 0, ms))
return loader_train, loader_test
