iaode 0.2.9

Interpretable Autoencoder with Ordinary Differential Equations for single-cell omics analysis

iAODE: Interpretable Accessibility ODE VAE for scATAC-seq

iAODE (Interpretable Accessibility ODE VAE) is a lightweight deep learning framework purpose-built for single‑cell ATAC‑seq (scATAC‑seq) data. It integrates a Variational Autoencoder (VAE) with a Neural ODE and an interpretable bottleneck to jointly achieve:

1. Robust Modeling: Handles sparse count accessibility profiles using Negative Binomial (NB) or Zero-Inflated Negative Binomial (ZINB) likelihoods.
2. Continuous Trajectory Inference: Infers dynamics via Neural ODE pseudotime and latent velocity fields.
3. Interpretable Latent Factors: Utilizes a biologically aligned bottleneck to extract meaningful features.
4. Scalable Preprocessing: Implements TF‑IDF normalization and Highly Variable Peak (HVP) selection, aligned with Signac and SnapATAC2 best practices.

The design specifically targets the unique characteristics of scATAC data, including extreme sparsity, library size variability, heterogeneous peak accessibility kinetics, and dynamic regulatory trajectories.

---

Core Architecture

Raw Peak Counts  --(TF-IDF)-->  Normalized Matrix  --(HVP Selection)-->  Peak Subset
       |
       v
Encoder (MLP / Residual / Transformer) --> q(z|x)
       |                 \
       |                  +--> Bottleneck (i_dim) -> Interpretable factors
       v
   Neural ODE f(z,t) -> z_ode(t)  (pseudotime + dynamics)
       |                \
       |                 +--> Consistency Loss (q_z vs z_ode)
       v
   Decoder (NB / ZINB / MSE) -> Reconstruction x_hat

Key Components:

• TF‑IDF Normalization: Stabilizes cell‑wise sequencing depth and highlights specific accessibility patterns.
• Highly Variable Peaks (HVP): Selects informative peaks using variance, VMR, or deviance‑based methods.
• NB/ZINB Likelihoods: Explicitly models over‑dispersion and zero inflation inherent in single-cell data.
• Neural ODE: Learns smooth accessibility progressions using pseudotime and velocity.
• Interpretable Bottleneck: A linear compression layer that preserves biologically decodable axes.
• Multi‑Objective Regularization: Includes $\beta$-VAE KL, $\beta$-TC, DIP, InfoVAE MMD, and ODE consistency losses.

Loss Function:

Loss = recon + i_recon + ODE_consistency + β·KL + dip·DIP + tc·TC + info·MMD

---

Installation

Method 1: Python Library (Standard)

For users using iAODE in scripts or notebooks:

pip install iaode

Method 2: Web Interface (Full)

For users who want the Interactive Training UI, you must clone the repository (since the UI requires the server files):

git clone https://github.com/PeterPonyu/iAODE.git
cd iAODE
pip install -e .
pip install fastapi uvicorn  # Required for the UI server

---

Quick Start

🖥️ Interactive Web Interface

No Node.js required. The interface is pre-built and served via Python.

1. Start the Server:

   python api/run_server.py
   

2. Access the UI: Open http://localhost:8000/ in your browser.

   Features:

   • Upload .h5ad or .h5 files.
   • Configure Encoders, Loss functions, and ODE parameters visually.
   • Download trained embeddings directly.

Basic scATAC-seq Workflow

import scanpy as sc
import iaode
from iaode.utils import tfidf_normalization, select_highly_variable_peaks
from iaode.annotation import load_10x_h5_data

# 1. Download and load scATAC-seq data (auto-cached)
h5_file, gtf_file = iaode.datasets.mouse_brain_5k_atacseq()
print(f"Data downloaded to: {h5_file.parent}")

# Load peak count matrix
adata = load_10x_h5_data(str(h5_file))
adata.layers['counts'] = adata.X.copy()
print(f"Loaded: {adata.n_obs} cells × {adata.n_vars} peaks")

# 2. TF-IDF normalization (Signac/SnapATAC2 best practice)
tfidf_normalization(
    adata,
    scale_factor=1e4,
    log_tf=False,
    log_idf=True,
    inplace=True
)

# 3. Highly variable peak (HVP) selection
select_highly_variable_peaks(
    adata,
    n_top_peaks=20000,
    method='signac',
    min_accessibility=0.01,
    max_accessibility=0.95,
    inplace=True
)

# Subset to HVPs
hvp_mask = adata.var['highly_variable']
adata = adata[:, hvp_mask].copy()
print(f"Retained {adata.n_vars} highly variable peaks")

# 4. Train iAODE model
model = iaode.agent(
    adata,
    layer='counts',
    latent_dim=32,         # Higher dimension for scATAC complexity
    hidden_dim=512,        # Deeper network for regulatory patterns
    encoder_type='mlp',
    loss_mode='zinb',      # Recommended for sparse scATAC data
    use_ode=False
)

model.fit(epochs=400, patience=25, val_every=10)

# 5. Extract latent representation
latent = model.get_latent()
adata.obsm['X_iaode'] = latent

# 6. Visualize with UMAP
sc.pp.neighbors(adata, use_rep='X_iaode')
sc.tl.umap(adata)

# Color by QC metrics
sc.pl.umap(adata, color=['n_genes_by_counts', 'total_counts'])

scATAC-seq with Trajectory Inference

import scanpy as sc
import iaode
from iaode.utils import tfidf_normalization, select_highly_variable_peaks
from iaode.annotation import load_10x_h5_data

# 1. Load and preprocess scATAC-seq data
h5_file, gtf_file = iaode.datasets.mouse_brain_5k_atacseq()
adata = load_10x_h5_data(str(h5_file))
adata.layers['counts'] = adata.X.copy()

# TF-IDF normalization
tfidf_normalization(adata, scale_factor=1e4, log_tf=False, log_idf=True, inplace=True)

# Select highly variable peaks
select_highly_variable_peaks(adata, n_top_peaks=20000, method='signac', inplace=True)
adata = adata[:, adata.var['highly_variable']].copy()

# 2. Train iAODE with Neural ODE for trajectory inference
model = iaode.agent(
    adata,
    layer='counts',
    use_ode=True,          # Enable Neural ODE dynamics
    i_dim=16,              # Interpretable bottleneck dimension
    latent_dim=32,
    hidden_dim=512,
    encoder_type='mlp',
    loss_mode='zinb'
)

model.fit(epochs=400, patience=25, val_every=10)

# 3. Extract trajectory-related representations
latent = model.get_latent()           # Latent space (z)
iembed = model.get_iembed()           # Interpretable regulatory factors
pseudotime = model.get_pseudotime()   # ODE time parameter
velocity = model.get_velocity()       # Latent velocity field

# Store in AnnData
adata.obsm['X_iaode'] = latent
adata.obsm['X_iembed'] = iembed
adata.obs['pseudotime'] = pseudotime
adata.obsm['velocity'] = velocity

# 4. Visualize trajectory
sc.pp.neighbors(adata, use_rep='X_iaode')
sc.tl.umap(adata)

# Color UMAP by pseudotime to reveal developmental trajectory
sc.pl.umap(adata, color='pseudotime', cmap='viridis')

# Visualize velocity field (requires UMAP coordinates)
E_grid, V_grid = model.get_vfres(
    adata,
    zs_key='X_iaode',
    E_key='X_umap',
    stream=True,
    density=1.5
)

import matplotlib.pyplot as plt
fig, ax = plt.subplots(figsize=(8, 6))
sc.pl.umap(adata, color='pseudotime', ax=ax, show=False)
ax.streamplot(E_grid[0], E_grid[1], V_grid[0], V_grid[1], 
              color='gray', density=1.5, linewidth=0.5, arrowsize=1)
plt.tight_layout()
plt.show()

scATAC-seq Peak Annotation Pipeline

Automatic Data Download - iAODE automatically downloads and caches datasets:

import iaode

# Download mouse brain 5k scATAC-seq + GENCODE vM25 GTF
# Files are cached in ~/.iaode/data/ and reused on subsequent runs
h5_file, gtf_file = iaode.datasets.mouse_brain_5k_atacseq()

# Run complete annotation pipeline
adata = iaode.annotation_pipeline(
    h5_file=str(h5_file),
    gtf_file=str(gtf_file),
    promoter_upstream=2000,  # TSS upstream region
    promoter_downstream=500, # TSS downstream region
    apply_tfidf=True,        # Apply TF-IDF normalization
    select_hvp=True,         # Select highly variable peaks
    n_top_peaks=20000        # Number of HVPs to retain
)

# The returned AnnData object contains:
# - adata.var['peak_type']: Annotation (promoter/exonic/intronic/intergenic)
# - adata.var['gene_name']: Associated gene names
# - adata.var['distance_to_tss']: Distance to nearest TSS
# - adata.var['highly_variable']: HVP selection mask
# - Preprocessed counts (TF-IDF)

Available Datasets:

# Mouse brain 5k scATAC-seq
h5, gtf = iaode.datasets.mouse_brain_5k_atacseq()

# Human PBMC 5k scATAC-seq
h5, gtf = iaode.datasets.human_pbmc_5k_atacseq()

# Cache management
iaode.datasets.list_cached_files()  # Show cached files
iaode.datasets.clear_cache()        # Clear all cached data

---

Examples

Comprehensive examples are provided in the examples/ directory. See examples/README.md for detailed documentation.

Example Scripts

Script	Purpose	Modality	Best For
basic_usage.py	scATAC-seq with 2D/histogram visualizations	scATAC	Getting started with scATAC-seq
atacseq_annotation.py	Peak-to-gene annotation + QC plots	scATAC	Understanding peak annotation
model_evaluation_atac.py	Benchmark iAODE vs scVI on scATAC-seq	scATAC	Comparative analysis (chromatin)
model_evaluation_rna.py	Benchmark iAODE vs scVI on scRNA-seq	scRNA	Comparative analysis (transcriptome)
trajectory_inference_atac.py	Neural ODE trajectory with scATAC-seq	scATAC	Chromatin accessibility dynamics
trajectory_inference_rna.py	Neural ODE trajectory with scRNA-seq	scRNA	Transcriptional trajectory

Running Examples

cd examples

# Getting started with scATAC-seq
python basic_usage.py

# Peak-to-gene annotation with auto-download
python atacseq_annotation.py

# Benchmark models on scATAC-seq data
python model_evaluation_atac.py

# Trajectory inference with Neural ODE (scRNA-seq)
python trajectory_inference_rna.py

By default, all examples save outputs to examples/outputs/<example_name>/.

---

API Reference

iaode.agent - Main Model Interface

Initialization:

model = iaode.agent(
    adata,                    # AnnData object
    layer='counts',           # Data layer to use (key in adata.layers or 'X')
    latent_dim=10,            # Latent space dimension
    hidden_dim=128,           # Hidden layer dimension
    i_dim=2,                  # Interpretable bottleneck dimension (default: 2)
    use_ode=False,            # Enable Neural ODE
    loss_mode='nb',           # Loss function: 'mse', 'nb', 'zinb'
    encoder_type='mlp',       # Encoder: 'mlp', 'mlp_residual', 'transformer', 'linear'
    lr=1e-4,                  # Learning rate
    batch_size=128,           # Batch size
    beta=1.0,                 # KL divergence weight
    recon=1.0,                # Reconstruction loss weight
    tc=0.0,                   # Total correlation weight
    dip=0.0,                  # DIP weight
    info=0.0                  # InfoVAE MMD weight
)

Training:

model.fit(
    epochs=100,               # Maximum epochs
    patience=20,              # Early stopping patience
    val_every=5,              # Validation frequency
    early_stop=True           # Enable early stopping
)

Representation Extraction:

# Basic representations
latent = model.get_latent()              # Latent space (n_cells, latent_dim)
iembed = model.get_iembed()              # Interpretable factors (n_cells, i_dim)

# Trajectory-specific (requires use_ode=True)
pseudotime = model.get_pseudotime()      # ODE time parameter (n_cells,)
velocity = model.get_velocity()          # Latent velocity (n_cells, latent_dim)

# Vector field for visualization (requires UMAP in adata.obsm['X_umap'])
E_grid, V_grid = model.get_vfres(
    adata,
    zs_key='X_iaode',        # Latent representation key
    E_key='X_umap',          # Embedding key for visualization
    stream=True,             # Return streamplot-compatible format
    density=1.5              # Grid density
)

Evaluation Metrics:

# Training metrics
metrics = model.get_resource_metrics()
# Returns: {'train_time': float, 'actual_epochs': int, 'peak_memory_gb': float}

---

iaode.annotation_pipeline - scATAC-seq Preprocessing

Complete annotation and preprocessing pipeline:

adata = iaode.annotation_pipeline(
    h5_file,                    # Path to 10X H5 file
    gtf_file,                   # Path to GTF annotation
    promoter_upstream=2000,     # TSS upstream extension (bp)
    promoter_downstream=500,    # TSS downstream extension (bp)
    apply_tfidf=True,           # Apply TF-IDF normalization
    select_hvp=True,            # Select highly variable peaks
    n_top_peaks=20000,          # Number of HVPs to retain
    hvp_method='signac',        # HVP method: 'signac', 'snapatac2', 'deviance'
    min_accessibility=0.01,     # Min peak accessibility fraction
    max_accessibility=0.95      # Max peak accessibility fraction
)

Returns AnnData with:

• adata.var['peak_type']: Peak annotation (promoter/exonic/intronic/intergenic)
• adata.var['gene_name']: Associated gene names
• adata.var['distance_to_tss']: Distance to nearest TSS
• adata.var['highly_variable']: HVP selection mask
• Preprocessed and normalized counts

---

Evaluation Functions

Dimensionality Reduction Quality

from iaode import evaluate_dimensionality_reduction

metrics = evaluate_dimensionality_reduction(
    X_high,                  # High-dimensional data (n_cells, n_features)
    X_low,                   # Low-dimensional embedding (n_cells, n_latent)
    k=10,                    # Number of neighbors
    verbose=True
)

# Returns:
# - distance_correlation: Global structure preservation (Spearman ρ)
# - Q_local: Local neighborhood quality
# - Q_global: Global structure quality
# - K_max: Local-global transition point

Latent Space Quality

from iaode import evaluate_single_cell_latent_space

metrics = evaluate_single_cell_latent_space(
    latent_space,            # Latent representation (n_cells, n_latent)
    data_type='trajectory',  # 'trajectory' or 'steady_state'
    verbose=True
)

# Returns:
# - manifold_dimensionality: Dimensional efficiency (0-1)
# - spectral_decay_rate: Eigenvalue concentration
# - participation_ratio: Dimensional balance
# - anisotropy_score: Directionality strength
# - trajectory_directionality: Dominant axis strength
# - noise_resilience: Signal-to-noise ratio
# - overall_quality: Aggregate score

Model Benchmarking

from iaode import DataSplitter, train_scvi_models, evaluate_scvi_models

# Create consistent train/val/test splits
splitter = DataSplitter(
    n_samples=adata.n_obs,
    test_size=0.15,
    val_size=0.15,
    random_state=42
)

# Train scVI family models
scvi_results = train_scvi_models(
    adata,
    splitter,
    n_latent=10,
    n_epochs=400,
    batch_size=128
)

# Evaluate all models
scvi_metrics = evaluate_scvi_models(
    scvi_results,
    adata,
    splitter.test_idx
)

---

Preprocessing Utilities

from iaode.utils import tfidf_normalization, select_highly_variable_peaks

# TF-IDF normalization (Signac/SnapATAC2 style)
tfidf_normalization(
    adata,
    scale_factor=1e4,
    log_tf=False,
    log_idf=True,
    inplace=True
)

# Highly variable peak selection
select_highly_variable_peaks(
    adata,
    n_top_peaks=20000,
    method='signac',         # or 'snapatac2', 'deviance'
    min_accessibility=0.01,
    max_accessibility=0.95,
    inplace=True
)

---

Advanced Usage

Custom Encoder Architecture

# Transformer encoder for large-scale data
model = iaode.agent(
    adata,
    encoder_type='transformer',
    encoder_num_layers=4,
    encoder_n_heads=8,
    encoder_d_model=256,
    hidden_dim=512,
    latent_dim=32
)

Multi-Objective Regularization

# Fine-tune regularization weights
model = iaode.agent(
    adata,
    recon=1.0,      # Reconstruction loss
    beta=1.0,       # KL divergence
    tc=0.5,         # Total correlation (disentanglement)
    dip=0.1,        # DIP (dimension-wise independence)
    info=0.05       # InfoVAE MMD (distribution matching)
)

Custom Training Loop

# Manual training with custom logic
for epoch in range(100):
    train_loss = model.train_epoch()
    
    if epoch % 5 == 0:
        val_loss, val_score = model.validate()
        print(f"Epoch {epoch}: Val Loss={val_loss:.4f}")
        
    if should_stop(val_loss):
        model.load_best_model()
        break

---

Citation

If you use iAODE in your research, please cite:

@software{iaode2025,
    author = {Zeyu Fu},
    title = {iAODE: Interpretable Accessibility ODE VAE for Single-Cell Chromatin Dynamics},
    year = {2025},
    publisher = {GitHub},
    url = {https://github.com/PeterPonyu/iAODE}
}

---

Contributing

Contributions are welcome! Please follow these steps:

1. Fork the repository.
2. Create a feature branch (git checkout -b feature/AmazingFeature).
3. Commit your changes (git commit -m 'Add AmazingFeature').
4. Push to the branch (git push origin feature/AmazingFeature).
5. Open a Pull Request.

For major changes, please open an issue first to discuss the proposed modifications.

---

License

This project is licensed under the MIT License - see the LICENSE file for details.

---

Acknowledgments

Built upon concepts from:

• scVI-tools: scVI, PEAKVI, and POISSONVI architectures.
• Signac and SnapATAC2: Best practices for scATAC-seq data processing.
• Neural ODE: Literature regarding continuous latent dynamics.

Foundational support is provided by the PyTorch, AnnData, and Scanpy ecosystems.

---

Contact

• GitHub Issues: https://github.com/PeterPonyu/iAODE/issues
• Email: [e-mail]

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Changelog

See CHANGELOG.md for detailed release notes and version history.