GeneCompass — Foundation Model Tutorial¶

GeneCompass — Prior-knowledge-enhanced pretraining (gene regulatory networks + pathway info), 120M cell training corpus

Property	Value
Tasks	embed, integrate
Species	human, mouse
Gene IDs	symbol
GPU Required	Yes
Min VRAM	16 GB
Embedding Dim	512
Repository	https://github.com/xCompass-AI/GeneCompass

This tutorial demonstrates how to use GeneCompass through the unified ov.fm API.

Cite: Zeng, Z. et al. (2024). OmicVerse: a framework for bridging and deepening insights across bulk and single-cell sequencing. Nature Communications, 15(1), 5983.

import omicverse as ov
import scanpy as sc
import os
import warnings
warnings.filterwarnings('ignore')

ov.plot_set()

Why GeneCompass?¶

GeneCompass is unique because it incorporates prior biological knowledge during pretraining:

Gene regulatory networks are baked into the model architecture
Pathway information from databases like KEGG and Reactome informs the embeddings
120M cell training corpus — one of the largest pretraining datasets
Cross-species — supports both human and mouse data natively

Choose GeneCompass when your analysis benefits from pathway-aware or GRN-informed embeddings.

Step 1: Inspect Model Specification¶

Use ov.fm.describe_model() to get the full spec for GeneCompass.

info = ov.fm.describe_model("genecompass")

print("=== Model Info ===")
print(f"Name: {info['model']['name']}")
print(f"Version: {info['model']['version']}")
print(f"Tasks: {info['model']['tasks']}")
print(f"Species: {info['model']['species']}")
print(f"Embedding dim: {info['model']['embedding_dim']}")
print(f"Differentiator: {info['model']['differentiator']}")

print("\n=== Input Contract ===")
print(f"Gene ID scheme: {info['input_contract']['gene_id_scheme']}")
print(f"Preprocessing: {info['input_contract']['preprocessing']}")

print("\n=== Output Contract ===")
print(f"Embedding key: {info['output_contract']['embedding_key']}")
print(f"Embedding dim: {info['output_contract']['embedding_dim']}")

Step 2: Prepare Data¶

Load a dataset and save it for the ov.fm workflow. Most foundation models expect raw counts (non-negative values).

adata = sc.datasets.pbmc3k()
sc.pp.filter_cells(adata, min_genes=200)
sc.pp.filter_genes(adata, min_cells=3)
print(f'Dataset: {adata.n_obs} cells x {adata.n_vars} genes')
print(f'Gene names (first 5): {adata.var_names[:5].tolist()}')
print(f'X range: [{adata.X.min():.1f}, {adata.X.max():.1f}]')

adata.write_h5ad('pbmc3k_genecompass.h5ad')

Step 3: Profile Data & Validate Compatibility¶

Check whether your data is compatible with GeneCompass before running inference.

profile = ov.fm.profile_data("pbmc3k_genecompass.h5ad")

print("=== Data Profile ===")
print(f"Species: {profile['species']}")
print(f"Gene scheme: {profile['gene_scheme']}")
print(f"Modality: {profile['modality']}")
print(f"Cells: {profile['n_cells']:,}")
print(f"Genes: {profile['n_genes']:,}")

# Validate compatibility
validation = ov.fm.preprocess_validate("pbmc3k_genecompass.h5ad", "genecompass", "embed")
print(f"\n=== Validation: {validation['status']} ===")
for d in validation.get("diagnostics", []):
    print(f"  [{d['severity']}] {d['message']}")
if validation.get("auto_fixes"):
    print("\nSuggested fixes:")
    for fix in validation["auto_fixes"]:
        print(f"  - {fix}")

Step 4: Run GeneCompass Inference¶

Execute GeneCompass through ov.fm.run(). The function handles preprocessing, model loading, inference, and output writing.

result = ov.fm.run(
    task="embed",
    model_name="genecompass",
    adata_path="pbmc3k_genecompass.h5ad",
    output_path="pbmc3k_genecompass_out.h5ad",
    device="auto",
)

if "error" in result:
    print(f"Error: {result['error']}")
    if "suggestion" in result:
        print(f"Suggestion: {result['suggestion']}")
else:
    print(f"Status: {result['status']}")
    print(f"Output keys: {result.get('output_keys', [])}")
    print(f"Cells processed: {result.get('n_cells', 0)}")

Step 5: Visualize & Interpret Results¶

Load the output, compute UMAP from GeneCompass embeddings, and evaluate quality.

if os.path.exists("pbmc3k_genecompass_out.h5ad"):
    adata_out = sc.read_h5ad("pbmc3k_genecompass_out.h5ad")
    emb_key = "X_genecompass"
    
    if emb_key in adata_out.obsm:
        print(f"Embedding shape: {adata_out.obsm[emb_key].shape}")
        
        # UMAP visualization
        sc.pp.neighbors(adata_out, use_rep=emb_key)
        sc.tl.umap(adata_out)
        sc.tl.leiden(adata_out, resolution=0.5)
        sc.pl.umap(adata_out, color=["leiden"],
                   title="GeneCompass Embedding (PBMC 3k)")
        
        # QA metrics
        interpretation = ov.fm.interpret_results("pbmc3k_genecompass_out.h5ad", task="embed")
        if "embeddings" in interpretation["metrics"]:
            for k, v in interpretation["metrics"]["embeddings"].items():
                print(f"\n{k}: dim={v['dim']}", end="")
                if "silhouette" in v:
                    print(f", silhouette={v['silhouette']:.4f}", end="")
                print()
    else:
        print(f"Embedding key {emb_key} not found.")
        print(f"Available keys: {list(adata_out.obsm.keys())}")
else:
    print("Output file not found — check model installation and adapter status.")
    print("See the Guide page for installation instructions.")

Summary¶

Step	Function	What it does
1	`ov.fm.describe_model("genecompass")`	Inspect model spec and I/O contract
2	`sc.datasets.pbmc3k()`	Prepare input data
3	`ov.fm.profile_data()` + `preprocess_validate()`	Check compatibility
4	`ov.fm.run()`	Execute GeneCompass inference
5	`ov.fm.interpret_results()`	Evaluate embedding quality

For the full model catalog, see ov.fm.list_models() or the ov.fm API Overview. For detailed GeneCompass specifications, see the GeneCompass Guide.