DeepChem API Reference

DeepChem API Reference

This document provides a comprehensive reference for DeepChem's core APIs, organized by functionality.

Data Handling

Data Loaders

File Format Loaders

• CSVLoader: Load tabular data from CSV files with customizable feature handling
• UserCSVLoader: User-defined CSV loading with flexible column specifications
• SDFLoader: Process molecular structure files (SDF format)
• JsonLoader: Import JSON-structured datasets
• ImageLoader: Load image data for computer vision tasks

Biological Data Loaders

• FASTALoader: Handle protein/DNA sequences in FASTA format
• FASTQLoader: Process FASTQ sequencing data with quality scores
• SAMLoader/BAMLoader/CRAMLoader: Support sequence alignment formats

Specialized Loaders

• DFTYamlLoader: Process density functional theory computational data
• InMemoryLoader: Load data directly from Python objects

Dataset Classes

• NumpyDataset: Wrap NumPy arrays for in-memory data manipulation
• DiskDataset: Manage larger datasets stored on disk, reducing memory overhead
• ImageDataset: Specialized container for image-based ML tasks

Data Splitters

General Splitters

• RandomSplitter: Random dataset partitioning
• IndexSplitter: Split by specified indices
• SpecifiedSplitter: Use pre-defined splits
• RandomStratifiedSplitter: Stratified random splitting
• SingletaskStratifiedSplitter: Stratified splitting for single tasks
• TaskSplitter: Split for multitask scenarios

Molecule-Specific Splitters

• ScaffoldSplitter: Divide molecules by structural scaffolds (prevents data leakage)
• ButinaSplitter: Clustering-based molecular splitting
• FingerprintSplitter: Split based on molecular fingerprint similarity
• MaxMinSplitter: Maximize diversity between training/test sets
• MolecularWeightSplitter: Split by molecular weight properties

Best Practice: For drug discovery tasks, use ScaffoldSplitter to prevent overfitting on similar molecular structures.

Transformers

Normalization

• NormalizationTransformer: Standard normalization (mean=0, std=1)
• MinMaxTransformer: Scale features to [0,1] range
• LogTransformer: Apply log transformation
• PowerTransformer: Box-Cox and Yeo-Johnson transformations
• CDFTransformer: Cumulative distribution function normalization

Task-Specific

• BalancingTransformer: Address class imbalance
• FeaturizationTransformer: Apply dynamic feature engineering
• CoulombFitTransformer: Quantum chemistry specific
• DAGTransformer: Directed acyclic graph transformations
• RxnSplitTransformer: Chemical reaction preprocessing

Molecular Featurizers

Graph-Based Featurizers

Use these with graph neural networks (GCNs, MPNNs, etc.):

• ConvMolFeaturizer: Graph representations for graph convolutional networks
• WeaveFeaturizer: "Weave" graph embeddings
• MolGraphConvFeaturizer: Graph convolution-ready representations
• EquivariantGraphFeaturizer: Maintains geometric invariance
• DMPNNFeaturizer: Directed message-passing neural network inputs
• GroverFeaturizer: Pre-trained molecular embeddings

Fingerprint-Based Featurizers

Use these with traditional ML (Random Forest, SVM, XGBoost):

• MACCSKeysFingerprint: 167-bit structural keys
• CircularFingerprint: Extended connectivity fingerprints (Morgan fingerprints)
  • Parameters: radius (default 2), size (default 2048), useChirality (default False)
• PubChemFingerprint: 881-bit structural descriptors
• Mol2VecFingerprint: Learned molecular vector representations

Descriptor Featurizers

Calculate molecular properties directly:

• RDKitDescriptors: ~200 molecular descriptors (MW, LogP, H-donors, H-acceptors, TPSA, etc.)
• MordredDescriptors: Comprehensive structural and physicochemical descriptors
• CoulombMatrix: Interatomic distance matrices for 3D structures

Sequence-Based Featurizers

For recurrent networks and transformers:

• SmilesToSeq: Convert SMILES strings to sequences
• SmilesToImage: Generate 2D image representations from SMILES
• RawFeaturizer: Pass through raw molecular data unchanged

Selection Guide

Models

Scikit-Learn Integration

• SklearnModel: Wrapper for any scikit-learn algorithm
  • Usage: SklearnModel(model=RandomForestRegressor())

Gradient Boosting

• GBDTModel: Gradient boosting decision trees (XGBoost, LightGBM)

PyTorch Models

Molecular Property Prediction

• MultitaskRegressor: Multi-task regression with shared representations
• MultitaskClassifier: Multi-task classification
• MultitaskFitTransformRegressor: Regression with learned transformations
• GCNModel: Graph convolutional networks
• GATModel: Graph attention networks
• AttentiveFPModel: Attentive fingerprint networks
• DMPNNModel: Directed message passing neural networks
• GroverModel: GROVER pre-trained transformer
• MATModel: Molecule attention transformer

Materials Science

• CGCNNModel: Crystal graph convolutional networks
• MEGNetModel: Materials graph networks
• LCNNModel: Lattice CNN for materials

Generative Models

• GANModel: Generative adversarial networks
• WGANModel: Wasserstein GAN
• BasicMolGANModel: Molecular GAN
• LSTMGenerator: LSTM-based molecule generation
• SeqToSeqModel: Sequence-to-sequence models

Physics-Informed Models

• PINNModel: Physics-informed neural networks
• HNNModel: Hamiltonian neural networks
• LNN: Lagrangian neural networks
• FNOModel: Fourier neural operators

Computer Vision

• CNN: Convolutional neural networks
• UNetModel: U-Net architecture for segmentation
• InceptionV3Model: Pre-trained Inception v3
• MobileNetV2Model: Lightweight mobile networks

Hugging Face Models

• HuggingFaceModel: General wrapper for HF transformers
• Chemberta: Chemical BERT for molecular property prediction
• MoLFormer: Molecular transformer architecture
• ProtBERT: Protein sequence BERT
• DeepAbLLM: Antibody large language models

Model Selection Guide

MoleculeNet Datasets

Quick access to 30+ benchmark datasets via dc.molnet.load_*() functions.

Classification Datasets

• load_bace(): BACE-1 inhibitors (binary classification)
• load_bbbp(): Blood-brain barrier penetration
• load_clintox(): Clinical toxicity
• load_hiv(): HIV inhibition activity
• load_muv(): PubChem BioAssay (challenging, sparse)
• load_pcba(): PubChem screening data
• load_sider(): Adverse drug reactions (multi-label)
• load_tox21(): 12 toxicity assays (multi-task)
• load_toxcast(): EPA ToxCast screening

Regression Datasets

• load_delaney(): Aqueous solubility (ESOL)
• load_freesolv(): Solvation free energy
• load_lipo(): Lipophilicity (octanol-water partition)
• load_qm7/qm8/qm9(): Quantum mechanical properties
• load_hopv(): Organic photovoltaic properties

Protein-Ligand Binding

• load_pdbbind(): Binding affinity data

Materials Science

• load_perovskite(): Perovskite stability
• load_mp_formation_energy(): Materials Project formation energy
• load_mp_metallicity(): Metal vs. non-metal classification
• load_bandgap(): Electronic bandgap prediction

Chemical Reactions

• load_uspto(): USPTO reaction dataset

Usage Pattern

tasks, datasets, transformers = dc.molnet.load_bbbp(
    featurizer='GraphConv',  # or 'ECFP', 'GraphConv', 'Weave', etc.
    splitter='scaffold',      # or 'random', 'stratified', etc.
    reload=False              # set True to skip caching
)
train, valid, test = datasets

Metrics

Common evaluation metrics available in dc.metrics:

Classification Metrics

• roc_auc_score: Area under ROC curve (binary/multi-class)
• prc_auc_score: Area under precision-recall curve
• accuracy_score: Classification accuracy
• balanced_accuracy_score: Balanced accuracy for imbalanced datasets
• recall_score: Sensitivity/recall
• precision_score: Precision
• f1_score: F1 score

Regression Metrics

• mean_absolute_error: MAE
• mean_squared_error: MSE
• root_mean_squared_error: RMSE
• r2_score: R² coefficient of determination
• pearson_r2_score: Pearson correlation
• spearman_correlation: Spearman rank correlation

Multi-Task Metrics

Most metrics support multi-task evaluation by averaging over tasks.

Training Pattern

Standard DeepChem workflow:

# 1. Load data
loader = dc.data.CSVLoader(tasks=['task1'], feature_field='smiles',
                           featurizer=dc.feat.CircularFingerprint())
dataset = loader.create_dataset('data.csv')

# 2. Split data
splitter = dc.splits.ScaffoldSplitter()
train, valid, test = splitter.train_valid_test_split(dataset)

# 3. Transform data (optional)
transformers = [dc.trans.NormalizationTransformer(dataset=train)]
for transformer in transformers:
    train = transformer.transform(train)
    valid = transformer.transform(valid)
    test = transformer.transform(test)

# 4. Create and train model
model = dc.models.MultitaskRegressor(n_tasks=1, n_features=2048, layer_sizes=[1000])
model.fit(train, nb_epoch=50)

# 5. Evaluate
metric = dc.metrics.Metric(dc.metrics.r2_score)
train_score = model.evaluate(train, [metric])
test_score = model.evaluate(test, [metric])

Common Patterns

Pattern 1: Quick Baseline with MoleculeNet

tasks, datasets, transformers = dc.molnet.load_tox21(featurizer='ECFP')
train, valid, test = datasets
model = dc.models.MultitaskClassifier(n_tasks=len(tasks), n_features=1024)
model.fit(train)

Pattern 2: Custom Data with Graph Networks

featurizer = dc.feat.MolGraphConvFeaturizer()
loader = dc.data.CSVLoader(tasks=['activity'], feature_field='smiles',
                           featurizer=featurizer)
dataset = loader.create_dataset('my_data.csv')
train, test = dc.splits.RandomSplitter().train_test_split(dataset)
model = dc.models.GCNModel(mode='classification', n_tasks=1)
model.fit(train)

Pattern 3: Transfer Learning with Pretrained Models

model = dc.models.GroverModel(task='classification', n_tasks=1)
model.fit(train_dataset)
predictions = model.predict(test_dataset)