HIV Inhibitor Molecule Classification using GNN

A Graph Neural Network with Graph Convolution Layers to classify and generate HIV inhibitor molecules

Overview

Data

The data for inhibitor molecules was obtained from MoleculeNet data repository. The file HIV.scv inclues experimentally measured abilities to inhibit HIV replication. This CSV includes three fields representing molecule smiles string, activity and HIV_active status. However the data is skewed in a way that there are 39684 samples for negative class (not HIV active) and 1443 samples for positive class (HIV active).

Following are some molecules visualized using RDKit Chem module.

Visualization of random HIV negative molecules

Visualization of random HIV positive molecules

These visualizations can be generated from the following code

from rdkit import Chem
from rdkit.Chem import Draw

# Convert SMILES to RDKit molecule object
molecules = [Chem.MolFromSmiles(smiles) for smiles in smiles]

# Draw the molecule into grid
img = Draw.MolsToGridImage(molecules, molsPerRow=3)

Dataset Preprocessing

To handle class imbalance, the dataset was preprocessed before loading into a PyTorch Dataset class. Oversampling was used on the positive samples and increased them upto 10101 samples. Class imbalance will further be addressed by weighted loss during training.

The processed data was then seperated into two csv files using sklearn.model_selection.train_test_split() with a random split of 80:20. The csv files are stored in data/train/raw and data/test/raw seperately for proper working of the torch_geometric.data.Dataset() class. According to documentation, the Dataset class processes the data in the raw folder and caches in root/processed as a .pt file.

To set up data for training run the preprocess.py file. The dataset.py file includes the class definition for the HIVDatset() object. Each molecule is saved as a PyTorch Geometric graph data object with node features, edge attributes, edge index and label. This is automated using DeepChem library featurizers. MolGraphConvFeaturizer() was used to extract different node level features using the SMILES string of a molecule. This requires RDKit to be installed. Some examples for features are Atom type, formal charge, hybridization, degree and chirality. The returned feature size is 30.

import deepchem as dc

# Initialize DeepChem featurizer
featurizer = dc.feat.MolGraphConvFeaturizer(use_edges=True)

# Generate features using DeepChem featurizers
out = featurizer.featurize(row["smiles"])

# Convert to PyG graph data
data = out[0].to_pyg_graph()

Model

I used a simple Graph Convolutional Network (GCN) model (Kipf et al. 2017) as documented in PyG official tutorials. My model includes 3 layers of torch_geometric.nn.GCNConv to generate node embeddings followed by two linear layers. I used a hidden size of 512 inside each convolutional layers. The linear layer block reduces this 512 channel embedding to 64 then to 2. This outputs a 2-vector. The implementation is found in the model.py file. The model takes feature size (Usually 30) as input.

Model Training

The training process is set up by first instantiating the train and test datset objects and dataloaders with BATCH_SIZE = 128. The model is initialized by passing FEATURE_SIZE = 30 and send to the training device. The model has 574146 trainable parameters. The following optimizer and loss combination is used for training. Class weights are used to handle class imbalance. I calculated the class weights according to the class ratio in the preprocessed dataset. I found that if the dataset is balanced after oversampling weighted loss was producing worse results, therefore it can be turned off using the boolean USE_WEIGHTED_LOSS.

# Weight calculation
# For negative class = 49785 / (39684 x 2) = 0.63
# For positive class = 49785 / (10101 x 2) = 2.46

# Loss function
if USE_WEIGHTED_LOSS:
    weights = torch.tensor([0.63, 2.46], dtype=torch.float32).to(device) # Class weights to handle class imbalance
    loss_fn = torch.nn.CrossEntropyLoss(weight=weights)
else:
    loss_fn = torch.nn.CrossEntropyLoss()

# Optimizer
optimizer = torch.optim.SGD(model.parameters(), lr=0.01, momentum=0.9)

# Learning rate decay
scheduler = torch.optim.lr_scheduler.ExponentialLR(optimizer, gamma=0.95)

The train_step() and test_step() functions include the code for generating predictions, updating weights and calculating metrics during the training loop. Also exponential learning rate decay is used.

During training using Google Colab, EPOCHS = 100 was used.

As of the current training iteration (2024 July 14) the model obtains a train accuracy of 79%, test accuracy of 81% and gives the following loss curves.

Improvements Due:

Next I will find the reason for the spikes in the test loss, and find ways to improve the F1 score which is 0.57. PyG graph classification tutorial recommends on using torch_geometric.nn.GraphConv (which includes neighborhood normalization), instead of torch_geometric.nn.GCNConv. A new model using these layers will be tried next.

Technologies used

• PyTorch Geometric
• RDKit
• DeepChem
• Google Colab

References

• PyTorch Geometric Graph Datasets
• DeepChem Featurizers
• PyTorch Geometric Graph Classification Tutorial