neural-optimiser 0.0.6

Batched optimisation algorithms for neural network potential driven molecular dynamics.

neural-optimiser

Batched optimisation algorithms for neural network potential–driven molecular structure relaxation on top of PyTorch Geometric.

Key features

• Batched per-conformer BFGS with per-atom max-step control.
• Early exit on convergence (fmax), explosion (fexit), or step cap (steps).
• Trajectory collection per step (batch.pos_dt, batch.forces_dt, batch.energies_dt) and converged properties (batch.pos, batch.energies, batch.forces).
• IO methods for RDkit molecules and ASE atoms objects.

Installation

Install from PyPi

pip install neural-optimiser

pip install neural-optimiser[mace]

Install from source (uv)

Prerequisites: Python 3.11/12, PyTorch and torch-geometric compatible with your environment.

Create a virtual environment and install the package:

uv venv .venv
source .venv/bin/activate
uv pip install -e .

Optional dev tools:

uv pip install -e ".[dev]"
uv run pre-commit install

Installation for specific calculators:

uv run install-mace

Note: RDKit and torch-geometric may require platform-specific wheels. If uv/pip cannot resolve them directly, install those dependencies first using appropriate channels and then install this package.

Quick Start

All of the code below and more is available in the tutorial.

Run a Simple Batched BFGS Optimisation

This example uses neural_optimiser.optimise._bfgs.BFGS, and a dummy calculator, neural_optimiser.calculators._rand.RandomCalculator.

from ase.build import molecule

from neural_optimiser.optimisers import BFGS
from neural_optimiser.calculators import RandomCalculator
from neural_optimiser.conformers import ConformerBatch

# Create a batch of molecules (each becomes a conformer)
atoms_list = [molecule("H2O"), molecule("NH3"), molecule("CH4")]
batch = ConformerBatch.from_ase(atoms_list, device="cpu")

# Configure optimiser and attach a calculator that provides forces
optimiser = BFGS(steps=10, fmax=0.05, fexit=500.0, max_step=0.04)
optimiser.calculator = RandomCalculator()

# Run optimisation
converged = optimiser.run(batch)
print("All Converged:", converged)
for i, (conv, nsteps) in enumerate(zip(batch.converged, batch.converged_step)):
    print(f"Conformer {i}: Converged: {conv}, On step {nsteps}")

# Trajectory [T, N, 3] and converged coordinates [N, 3]
print("pos_dt shape:", tuple(batch.pos_dt.shape))
print("pos shape:", tuple(batch.pos.shape))

Notes:

• fmax triggers convergence per conformer using the maximum per-atom force norm,. Ether fmax or steps must be specified.
• fexit triggers early exit if all non-converged conformers exceed the threshold.
• Trajectories are accumulated in memory as batch.pos_dt along with their energies and forces (batch.forces_dt, batch.energies_dt); converged geometries are indexed into batch.pos, batch.energies, batch.forces (final positions are returned for non-converged conformers). See neural_optimiser.optimise.base.Optimiser for more details.

Run a Larger BFGS Optimisation using the ConformerDataLoader

For large datasets all your conformers may not fit in memory at once. In this case you can use the neural_optimiser.datasets.base.ConformerDataLoader to stream conformers in mini-batches.

from rdkit import Chem
from rdkit.Chem import AllChem

from neural_optimiser.conformers import Conformer, ConformerBatch
from neural_optimiser.datasets.base import ConformerDataset, ConformerDataLoader
from neural_optimiser.optimisers import BFGS
from neural_optimiser.calculators import RandomCalculator

# Build a pool of conformers from RDKit molecules
smiles_list = ["CCO", "CC", "CCN"]
mols = []
for smiles in smiles_list:
    m = Chem.AddHs(Chem.MolFromSmiles(smiles))
    AllChem.EmbedMultipleConfs(m, numConfs=10, useExpTorsionAnglePrefs=True, useBasicKnowledge=True)
    mols.append(m)

big_batch = ConformerBatch.from_rdkit(mols)  # creates one Conformer per RDKit conformer

# Dataset/DataLoader -> yields ConformerBatch
dataset = ConformerDataset(big_batch.to_data_list())
dataloader = ConformerDataLoader(dataset, batch_size=8, device="cpu", shuffle=True, num_workers=0)

# Configure optimiser and attach a calculator that provides forces
optimiser = BFGS(steps=10, fmax=0.05, fexit=500.0, max_step=0.04)
optimiser.calculator = RandomCalculator()

for batch in dataloader:
    optimiser.run(batch)

Using Your Own Calculator

Implement a calculator by subclassing neural_optimiser.calculators.base.Calculator and returning energies and forces for the full batch.

import torch
from torch_geometric.data import Batch, Data
from neural_optimiser.calculators.base import Calculator

class MyCalculator(Calculator):
    def _calculate(self, batch: Data | Batch) -> tuple[torch.Tensor, torch.Tensor]:
        # energies: required shape [N_atoms]
        energies = torch.zeros(batch.n_conformers, device=self.device, dtype=torch.float32)
        # forces: required shape [N_atoms, 3] matching batch.pos
        forces = torch.zeros_like(batch.pos, device=self.device)
        # ... fill forces from your model ...
        return energies, forces

    def to_atomic_data():
        pass

    def from_atomic_data():
        pass

Data Containers

Conformer

Molecules with 3D geometries are stored as neural_optimiser.conformers._conformer.Conformer objects.

from ase.build import molecule
from rdkit import Chem
from rdkit.Chem import AllChem
from neural_optimiser.conformers import Conformer

# From ASE
atoms = molecule("H2O")
conf1 = Conformer.from_ase(atoms, smiles="O")

print(type(conf1).__name__)
print("atom_types:", conf1.atom_types.shape)  # [n_atoms]
print("pos:", conf1.pos.shape)                # [n_atoms, 3]
print("smiles:", conf1.smiles)

# Convert back to ASE
atoms2 = conf1.to_ase()
print("ASE atoms:", atoms2.get_chemical_formula(), atoms2.positions.shape)

# From RDKit
mol = Chem.MolFromSmiles("CCO")
mol = Chem.AddHs(mol)
AllChem.EmbedMolecule(mol, AllChem.ETKDG())
conf2 = Conformer.from_rdkit(mol)

# Convert back to RDKit (returns a Mol with one 3D conformer)
mol2 = conf2.to_rdkit()
print("RDKit confs:", mol2.GetNumConformers())

ConformerBatch

Different molecules, or conformers of the same molecule (or both) can be stored in a neural_optimiser.conformers._conformer_batch.ConformerBatch object.

from ase.build import molecule
from rdkit import Chem
from rdkit.Chem import AllChem
from neural_optimiser.conformers import Conformer, ConformerBatch

# Build from ASE
atoms_list = [molecule("H2O"), molecule("NH3"), molecule("CH4")]
batch_ase = ConformerBatch.from_ase(atoms_list, device="cpu")
print("ASE batch:", batch_ase.n_molecules, batch_ase.n_conformers, batch_ase.n_atoms)

# Slice a single conformer view
conf0 = batch_ase.conformer(0)
print("conf0 pos:", conf0.pos.shape)

# Indices available on the batch (per-atom)
print("batch index shape:", batch_ase.batch.shape)
print("molecule_idxs shape:", batch_ase.molecule_idxs.shape)

# Build from RDKit (multiple conformers per molecule also supported)
def rdkit_with_coords(smiles: str):
    m = Chem.MolFromSmiles(smiles)
    m = Chem.AddHs(m)
    AllChem.EmbedMolecule(m, AllChem.ETKDG())
    return m

mol_list = [rdkit_with_coords("O"), rdkit_with_coords("CCO")]
batch_rd = ConformerBatch.from_rdkit(mol_list, device="cpu")
print("RDKit batch:", batch_rd.n_molecules, batch_rd.n_conformers, batch_rd.n_atoms)

# Build from a list of Conformer objects
c1 = Conformer.from_ase(molecule("H2O"))
c2 = Conformer.from_ase(molecule("NH3"))
batch_list = ConformerBatch.from_data_list([c1, c2], device="cpu")
print("Data list batch:", batch_list.n_molecules, batch_list.n_conformers, batch_list.n_atoms)

Testing

uv run pytest tests/

License

Apache 2.0 - see LICENSE.