A Standardized Framework for Evaluating Gene Expression Generative Models. Accepted at Gen2 Workshop @ ICLR 2026. Provides explicit computation space options (raw/pca/deg), perturbation-effect correlation, and standardized reporting for reproducible benchmarking.
Project description
GGE: A Standardized Framework for Evaluating Gene Expression Generative Models
Paper: Accepted at the Gen2 Workshop at ICLR 2026
Comprehensive, standardized evaluation of generated gene expression data.
GGE (Generated Genetic Expression Evaluator) addresses the urgent need for standardized evaluation in single-cell gene expression generative models. Current practices suffer from inconsistent metric implementations, incomparable hyperparameter choices, and lack of biologically-grounded metrics. GGE provides:
- Comprehensive suite of distributional metrics with explicit computation space options
- Biologically-motivated evaluation through DEG-focused analysis with perturbation-effect correlation
- Standardized reporting for reproducible benchmarking
Key Differentiators
| Feature | GGE | Others |
|---|---|---|
| Explicit space control (raw/pca/deg) | ✓ | — |
| Perturbation-effect correlation | ✓ | — |
| Configurable DEG thresholds | ✓ | — |
| GPU (CUDA) & Apple MPS acceleration | ✓ | Limited |
| Per-gene & aggregate metrics | ✓ | Varies |
| Visualization module | ✓ | — |
| Single Python API call | ✓ | Multi-step |
Features
Metrics
All metrics are computed per-gene (returning a vector) and aggregated:
| Metric | Description | Direction |
|---|---|---|
| Pearson Correlation | Linear correlation between expression profiles | Higher is better |
| Spearman Correlation | Rank correlation (robust to outliers) | Higher is better |
| R² | Coefficient of determination | Higher is better |
| Perturbation-Effect Correlation | Correlation on (real - ctrl) vs (gen - ctrl) | Higher is better |
| MSE | Mean Squared Error | Lower is better |
| Wasserstein-1 | Earth Mover's Distance (L1) | Lower is better |
| Wasserstein-2 | Sinkhorn-regularized OT | Lower is better |
| MMD | Maximum Mean Discrepancy (RBF kernel) | Lower is better |
| Energy Distance | Statistical potential energy | Lower is better |
Visualizations
- Boxplots & Violin plots: Metric distributions across conditions
- Radar plots: Multi-metric comparison
- Scatter plots: Real vs generated expression
- Embedding plots: PCA/UMAP of real vs generated data
- Heatmaps: Per-gene metric values
- Interactive Plotly plots: Density overlays, embeddings with metadata coloring
Computation Spaces
GGE treats computation space as a first-class parameter (see Paper Section 3.3):
| Space | Description | When to Use |
|---|---|---|
| Raw Gene Space | Full ~5,000–20,000 gene dimensions | Gene-level interpretability needed |
| PCA Space | Reduced k-dimensional space (default: 50) | Primary distributional metrics |
| DEG Space | Restricted to differentially expressed genes | Biologically-targeted evaluation |
Recommendation: Use multi-space evaluation—PCA-50 for distributional metrics, DEG for biological focus.
Key Features
- ✅ Explicit configuration: Every choice exposed as a parameter
- ✅ Universal space support: All metrics work in all spaces
- ✅ Condition-aware evaluation: Per condition (cell type × perturbation)
- ✅ Perturbation-effect correlation: Measures direction & magnitude of effects
- ✅ Hardware acceleration: GPU (CUDA) and Apple MPS support
- ✅ Lazy data loading: On-demand loading to avoid memory overhead
- ✅ Publication-quality visualizations: Static and interactive plots
Installation
pip install gge-eval
The package includes GPU-accelerated metrics via geomloss, which automatically falls back to CPU if no GPU is available.
Quick Start
Python API
from gge import evaluate
# From file paths
results = evaluate(
real_data="real_data.h5ad",
generated_data="generated_data.h5ad",
condition_columns=["perturbation", "cell_type"],
split_column="split", # Optional: for train/test
output_dir="evaluation_output/"
)
# From AnnData objects
import scanpy as sc
real_adata = sc.read_h5ad("real_data.h5ad")
generated_adata = sc.read_h5ad("generated_data.h5ad")
results = evaluate(
real_data=real_adata,
generated_data=generated_adata,
condition_columns=["perturbation"],
)
# Mixed (path + AnnData)
results = evaluate(
real_data="real_data.h5ad",
generated_data=generated_adata,
condition_columns=["perturbation"],
)
# Access results
print(results.summary())
# Get metric for specific split
test_results = results.get_split("test")
for condition, cond_result in test_results.conditions.items():
print(f"{condition}: Pearson={cond_result.get_metric_value('pearson'):.3f}")
Command Line
# Basic usage
gge --real real.h5ad --generated generated.h5ad \
--conditions perturbation cell_type \
--output results/
# With split column
gge --real real.h5ad --generated generated.h5ad \
--conditions perturbation \
--split-column split \
--splits test \
--output results/
# Specify metrics
gge --real real.h5ad --generated generated.h5ad \
--conditions perturbation \
--metrics pearson spearman wasserstein_1 mmd r_squared \
--output results/
DEG-Space Evaluation
GGE supports evaluating generative models specifically on differentially expressed genes (DEGs), which focuses the evaluation on the genes that matter most for capturing perturbation effects (Paper Section 4.3).
The Problem: Computing correlation on raw expression means can be artificially high if control and perturbed conditions have similar expression—dominated by genes similarly expressed across conditions.
The Solution: Perturbation-Effect Correlation (Paper Equation 1):
ρ_effect = corr(μ_real - μ_ctrl, μ_gen - μ_ctrl)
This measures whether models capture the direction and magnitude of perturbation effects, not just absolute expression levels.
from gge import (
evaluate_deg_space,
identify_degs,
compute_perturbation_effects,
compute_perturbation_effect_correlation,
)
import scanpy as sc
real_adata = sc.read_h5ad("real_data.h5ad")
generated_adata = sc.read_h5ad("generated_data.h5ad")
# Evaluate in DEG space (automatically identifies DEGs)
results, deg_info = evaluate_deg_space(
real_data=real_adata,
generated_data=generated_adata,
condition_columns=["perturbation"],
deg_condition_column="perturbation", # Column for DEG identification
control_value="control", # Control condition label
log2fc_threshold=1.0, # |log2FC| > 1
pvalue_threshold=0.05, # Adjusted p-value < 0.05
return_degs=True,
)
# View identified DEGs
print(f"Found {deg_info['is_deg'].sum()} DEGs")
deg_genes = deg_info[deg_info['is_deg']]['gene'].tolist()
# Compute perturbation-effect correlation (Paper Eq. 1)
control_mask = real_adata.obs['perturbation'] == 'control'
control_mean = real_adata[control_mask].X.mean(axis=0)
perturbed_mask = real_adata.obs['perturbation'] != 'control'
rho_effect = compute_perturbation_effect_correlation(
real_perturbed=real_adata[perturbed_mask].X,
generated_perturbed=generated_adata[perturbed_mask].X,
control_mean=control_mean,
method="pearson", # or "spearman"
)
print(f"Perturbation-effect correlation: {rho_effect:.3f}")
# Compute fold changes for analysis
effects = compute_perturbation_effects(
real_adata,
condition_column="perturbation",
control_value="control",
)
PC-Space Evaluation
For comparing global structure efficiently, GGE provides PC-space (principal component) evaluation (see Paper Section 3.3):
from gge import evaluate_pc_space, compute_pca, PCSpaceEvaluator
# Quick evaluation in PC space
results = evaluate_pc_space(
real_data=real_adata,
generated_data=generated_adata,
condition_columns=["perturbation"],
n_components=50, # Number of PCs
use_highly_variable=True, # Filter to HVGs first
n_top_genes=2000, # Number of HVGs
)
print(results.summary())
# Or use the evaluator class for more control
evaluator = PCSpaceEvaluator(n_components=50)
real_pc, gen_pc = evaluator.transform_to_pc_space(real_adata, generated_adata)
# Access PC coordinates
real_coords = real_pc.obsm['X_pca'] # shape: (n_samples, n_components)
gen_coords = gen_pc.obsm['X_pca']
# Compute PCA on a single dataset
adata_pca = compute_pca(real_adata, n_components=50)
Combined Evaluation Strategy
For comprehensive evaluation, combine gene-space, DEG-space, and PC-space metrics:
from gge import evaluate, evaluate_deg_space, evaluate_pc_space
# 1. Full gene-space evaluation
gene_results = evaluate(
real_data=real_adata,
generated_data=generated_adata,
condition_columns=["perturbation"],
metrics=["pearson", "spearman", "r_squared", "wasserstein_1", "mmd"],
)
# 2. DEG-space evaluation (perturbation-focused)
deg_results, degs = evaluate_deg_space(
real_data=real_adata,
generated_data=generated_adata,
condition_columns=["perturbation"],
deg_condition_column="perturbation",
control_value="control",
return_degs=True,
)
# 3. PC-space evaluation (global structure)
pc_results = evaluate_pc_space(
real_data=real_adata,
generated_data=generated_adata,
condition_columns=["perturbation"],
n_components=50,
)
print("Gene-space:", gene_results.summary())
print("DEG-space:", deg_results.summary())
print("PC-space:", pc_results.summary())
Expected Data Format
GGE expects AnnData (h5ad) files with:
Required
adata.X: Gene expression matrix (samples × genes)adata.var_names: Gene identifiers (must overlap between datasets)adata.obs[condition_columns]: Columns for matching conditions
Optional
adata.obs[split_column]: Train/test split indicator
Output Structure
output/
├── summary.json # Aggregate metrics and metadata
├── results.csv # Per-condition metrics table
├── per_gene_*.csv # Per-gene metric values
└── plots/
├── boxplot_metrics.png
├── violin_metrics.png
├── radar_split.png
├── scatter_grid.png
└── embedding_pca.png
Contributing
Contributions are welcome! Please feel free to submit a pull request or open an issue.
Citation
If you use GGE in your research, please cite our paper:
@inproceedings{rubbi2026gge,
title = {A Standardized Framework for Evaluating Gene Expression Generative Models},
author = {Rubbi, Andrea},
booktitle = {Gen2 Workshop at the International Conference on Learning Representations (ICLR)},
year = {2026},
url = {https://github.com/AndreaRubbi/GGE}
}
License
This project is licensed under the MIT License. See the LICENSE file for details.
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