---
name: deepchem
description: Molecular ML with diverse featurizers and pre-built datasets. Use for property prediction (ADMET, toxicity) with traditional ML or GNNs when you want extensive featurization options and MoleculeNet benchmarks. Best for quick experiments with pre-trained models, diverse molecular representations. For ready-made ADMET numbers without training a model use admet-prediction; for benchmark datasets and task-aware splits use pytdc.
license: MIT
allowed-tools: Read Write Edit Bash
compatibility: Requires Python 3.7–3.11 (PyPI 2.8.0 caps at <3.12). Install PyTorch, TensorFlow, or JAX before the matching deepchem extra. RDKit is a core dependency.
metadata:
  version: "1.6"
  skill-author: K-Dense Inc.
---

# DeepChem

## Overview

DeepChem is a comprehensive Python library for applying machine learning to chemistry, materials science, and biology. Enable molecular property prediction, drug discovery, materials design, and biomolecule analysis through specialized neural networks, molecular featurization methods, and pretrained models.

**Checked against:** deepchem **2.8.0** (PyPI stable, released 2024-04-02; still the current
release as of August 2026). Requires **Python 3.7–3.11** (`<3.12` on PyPI). Core utilities (loaders, featurizers, MoleculeNet) work without a DL backend; GNN and transformer models need the matching extra (`torch`, `tensorflow`, or `jax`). Install the backend framework first when using GPU builds.

**The release you install is much older than the code you will read about.** The GitHub
repository is actively developed, but 2.8.0 (April 2024) is still the newest tagged release, so
`pip install deepchem` gives you code roughly two years behind `master` while the online docs and
tutorials describe `master`. If an API in the documentation does not exist in your install, that
gap is the reason. Either pin to 2.8.0 and use the 2.8.0 docs, or install from git
(`pip install git+https://github.com/deepchem/deepchem.git`) and accept an untagged build.

## When to Use This Skill

This skill should be used when:
- Loading and processing molecular data (SMILES strings, SDF files, protein sequences)
- Predicting molecular properties (solubility, toxicity, binding affinity, ADMET properties)
- Training models on chemical/biological datasets
- Using MoleculeNet benchmark datasets (Tox21, BBBP, Delaney, etc.)
- Converting molecules to ML-ready features (fingerprints, graph representations, descriptors)
- Implementing graph neural networks for molecules (GCN, GAT, MPNN, AttentiveFP)
- Applying transfer learning with pretrained models (ChemBERTa, GROVER, MolFormer)
- Predicting crystal/materials properties (bandgap, formation energy)
- Analyzing protein or DNA sequences

## Core Capabilities

Eight capability areas, each with worked code, are in
[references/core_capabilities.md](references/core_capabilities.md):

1. **Molecular data loading and processing** — loaders, `NumpyDataset` / `DiskDataset`.
2. **Molecular featurization** — circular fingerprints, graph convolution, and descriptors.
3. **Data splitting** — random, scaffold, stratified, and butina splitters, and why
   scaffold splitting is the honest default for molecules.
4. **Model selection and training** — the model families and how to fit them.
5. **MoleculeNet benchmarks** — loading standard datasets and their published splits.
6. **Transfer learning** — pretraining and fine-tuning.
7. **Model evaluation** — metrics appropriate to regression and classification tasks.
8. **Making predictions** — applying a trained model to new molecules.

Three end-to-end workflows are in
[references/typical_workflows.md](references/typical_workflows.md).

## Example Scripts

This skill includes three production-ready scripts in the `scripts/` directory:

### 1. `predict_solubility.py`
Train and evaluate solubility prediction models. Works with Delaney benchmark or custom CSV data.

```bash
# Use Delaney benchmark
python scripts/predict_solubility.py

# Use custom data
python scripts/predict_solubility.py \
    --data my_data.csv \
    --smiles-col smiles \
    --target-col solubility \
    --predict "CCO" "c1ccccc1"
```

### 2. `graph_neural_network.py`
Train various graph neural network architectures on molecular data.

```bash
# Train GCN on Tox21
python scripts/graph_neural_network.py --model gcn --dataset tox21

# Train AttentiveFP on custom data
python scripts/graph_neural_network.py \
    --model attentivefp \
    --data molecules.csv \
    --task-type regression \
    --targets activity \
    --epochs 100
```

### 3. `transfer_learning.py`
Fine-tune pretrained models (ChemBERTa, GROVER, MolFormer) on molecular property prediction tasks.

```bash
# Fine-tune ChemBERTa on BBBP
python scripts/transfer_learning.py --model chemberta --dataset bbbp

# Fine-tune GROVER on custom data
python scripts/transfer_learning.py \
    --model grover \
    --data small_dataset.csv \
    --target activity \
    --task-type classification \
    --epochs 20
```

## Common Patterns and Best Practices

### Pattern 1: Always Use Scaffold Splitting for Molecules
```python
# GOOD: Prevents data leakage
splitter = dc.splits.ScaffoldSplitter()
train, test = splitter.train_test_split(dataset)

# BAD: Similar molecules in train and test
splitter = dc.splits.RandomSplitter()
train, test = splitter.train_test_split(dataset)
```

### Pattern 2: Normalize Features and Targets
```python
transformers = [
    dc.trans.NormalizationTransformer(
        transform_y=True,  # Also normalize target values
        dataset=train
    )
]
for transformer in transformers:
    train = transformer.transform(train)
    test = transformer.transform(test)
```

### Pattern 3: Start Simple, Then Scale
1. Start with Random Forest + CircularFingerprint (fast baseline)
2. Try XGBoost/LightGBM if RF works well
3. Move to deep learning (MultitaskRegressor) if you have >5K samples
4. Try GNNs if you have >10K samples
5. Use transfer learning for small datasets or novel scaffolds

### Pattern 4: Handle Imbalanced Data
```python
# Option 1: Balancing transformer
transformer = dc.trans.BalancingTransformer(dataset=train)
train = transformer.transform(train)

# Option 2: Use balanced metrics
metric = dc.metrics.Metric(dc.metrics.balanced_accuracy_score)
```

### Pattern 5: Avoid Memory Issues
```python
# Use DiskDataset for large datasets
dataset = dc.data.DiskDataset.from_numpy(X, y, w, ids)

# Use smaller batch sizes
model = dc.models.GCNModel(batch_size=32)  # Instead of 128
```

## Common Pitfalls

### Issue 1: Data Leakage in Drug Discovery
**Problem**: Using random splitting allows similar molecules in train/test sets.
**Solution**: Always use `ScaffoldSplitter` for molecular datasets.

### Issue 2: GNN Underperforming vs Fingerprints
**Problem**: Graph neural networks perform worse than simple fingerprints.
**Solutions**:
- Ensure dataset is large enough (>10K samples typically)
- Increase training epochs (50-100)
- Try different architectures (AttentiveFP, DMPNN instead of GCN)
- Use pretrained models (GROVER)

### Issue 3: Overfitting on Small Datasets
**Problem**: Model memorizes training data.
**Solutions**:
- Use stronger regularization (increase dropout to 0.5)
- Use simpler models (Random Forest instead of deep learning)
- Apply transfer learning (ChemBERTa, GROVER)
- Collect more data

### Issue 4: Import Errors
**Problem**: `No module named 'torch'` / `No module named 'tensorflow'` warnings, or model classes fail to import.
**Solution**: DeepChem loads lazily — install the backend that matches your model, then add the matching extra:
```bash
uv pip install deepchem              # loaders, featurizers, MoleculeNet only
uv pip install 'deepchem[torch]'       # GCN, GAT, AttentiveFP, HuggingFaceModel, GroverModel
uv pip install 'deepchem[tensorflow]'  # legacy Keras models
uv pip install 'deepchem[jax]'         # Haiku/JAX models
```
Install PyTorch or TensorFlow with the correct CUDA build **before** the extra when using GPUs. Quote extras in zsh: `'deepchem[torch]'`.

**Conda + PyTorch users:** If `import deepchem` fails with `undefined symbol: iJIT_NotifyEvent`, pin MKL below 2025 (`conda install "mkl<2025"`) — PyTorch wheels may be incompatible with MKL 2025.0.0.

## Reference Documentation

This skill includes comprehensive reference documentation:

### `references/api_reference.md`
Complete API documentation including:
- All data loaders and their use cases
- Dataset classes and when to use each
- Complete featurizer catalog with selection guide
- Model catalog organized by category (50+ models)
- MoleculeNet dataset descriptions
- Metrics and evaluation functions
- Common code patterns

**When to reference**: Search this file when you need specific API details, parameter names, or want to explore available options.

### `references/workflows.md`
Eight detailed end-to-end workflows:
1. Molecular property prediction from SMILES
2. Using MoleculeNet benchmarks
3. Hyperparameter optimization
4. Transfer learning with pretrained models
5. Molecular generation with GANs
6. Materials property prediction
7. Protein sequence analysis
8. Custom model integration

**When to reference**: Use these workflows as templates for implementing complete solutions.

## Installation

Core package (data loaders, featurizers, MoleculeNet, scikit-learn wrappers):

```bash
uv pip install deepchem
```

Add the extra that matches your model backend (install PyTorch/TensorFlow/JAX first for GPU builds):

```bash
uv pip install 'deepchem[torch]'       # GNNs, TorchModel, HuggingFaceModel, GroverModel
uv pip install 'deepchem[tensorflow]'  # Keras/TensorFlow models
uv pip install 'deepchem[jax]'         # JAX/Haiku models
uv pip install 'deepchem[dqc]'         # Differentiable quantum chemistry (torch + xitorch)
```

Nightly builds: `uv pip install --pre deepchem` (same extras apply with `--pre`).

See [installation guide](https://deepchem.readthedocs.io/en/latest/get_started/installation.html) and [soft requirements](https://deepchem.readthedocs.io/en/latest/requirements.html) for optional dependencies per model class.

## Composing with the rest of the bundle

- `admet-prediction` → instead, usually: if you want ADMET numbers rather than a trained model,
  ADMET-AI gives you 41 endpoints with approved-drug percentiles and no training run. Come here
  when you have your own measured data.
- `pytdc` → before: the datasets and, more importantly, the **task-aware splits**. A random split
  on molecular data reports a fantasy R²; scaffold splits are the reason to use PyTDC's loaders
  rather than rolling your own.
- `chembl` → before: the measured bioactivity to train on, curated rather than raw.
- `rdkit` / `datamol` → before: standardise and desalt. A featurizer will happily embed a salt.
- `molfeat` → alongside: a wider featurizer catalogue with a consistent interface, if
  featurization rather than model fitting is the bottleneck.
- `medchem` → after: a model's top-ranked generated molecules still need alert triage.

**Train on your own data or do not train.** A public benchmark model applied to your chemistry is
out of domain by construction; that is the case for `admet-prediction` instead.

## Additional Resources

- Official documentation: https://deepchem.readthedocs.io/
- GitHub repository: https://github.com/deepchem/deepchem
- Tutorials: https://deepchem.readthedocs.io/en/latest/get_started/tutorials.html
- Paper: "MoleculeNet: A Benchmark for Molecular Machine Learning"