PyGAGE 1.0.0

Python version of the GAGE (Generally Applicable Gene Set Enrichment) analysis package.

pygage - GAGE Analysis in Python

Python version of the GAGE (Generally Applicable Gene Set Enrichment) analysis package.

Overview

Uses Python modules using:

• polars for fast dataframe operations (instead of pandas)
• seaborn/matplotlib for visualization
• scipy for statistical tests
• argparse for command-line interfaces
• numpy for numerical operations

Installation

Quick install

pip install pygage

Custom install

# Clone repository
git clone https://github.com/raw-lab/pygage
cd pygage

# Install dependencies
pip install polars numpy scipy matplotlib seaborn requests
pip install .

Modules

1. gene_id_utils.py

Convert between Entrez Gene IDs and gene symbols.

Usage:

# Convert Entrez IDs to symbols
pygage-gene_id_utils.py input_ids.txt \
    --mapping egSymb.csv \
    --direction eg2sym \
    --output output_symbols.csv

# Convert symbols to Entrez IDs
pygage-gene_id_utils.py input_symbols.txt \
    --mapping egSymb.csv \
    --direction sym2eg \
    --output output_ids.csv

Python API:

from pygage.gene_id_utils import GeneIDConverter

converter = GeneIDConverter('egSymb.csv')
symbols = converter.eg2sym(['1', '2', '3'])
entrez_ids = converter.sym2eg(['TP53', 'BRCA1', 'EGFR'])

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2. pathway_database_utils.py

Retrieve gene sets from KEGG and Gene Ontology databases.

Usage:

# Retrieve KEGG pathways
pygage-pathway_database_utils.py kegg \
    --species hsa \
    --id-type entrez \
    --output kegg_pathways.json

# Retrieve GO gene sets
pygage-pathway_database_utils.py go \
    --annotation-file goa_human.gaf \
    --species human \
    --output go_genesets.json

Python API:

from pygage.pathway_database_utils import KEGGPathwayRetriever, GOGeneSetRetriever

# KEGG
kegg = KEGGPathwayRetriever()
pathways = kegg.get_pathway_genes(species='hsa', id_type='entrez')

# GO
go = GOGeneSetRetriever()
gene_sets = go.get_go_gene_sets(species='human', annotation_file='goa_human.gaf')

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3. visualization_utils.py

Create heatmaps, Venn diagrams, and color palettes.

Usage:

# Create Venn diagram
pygage-visualization_utils.py venn \
    --input comparison_data.csv \
    --names "Sample1" "Sample2" "Sample3" \
    --include both \
    --output venn_diagram.png

# Create heatmap
pygage-visualization_utils.py heatmap \
    --input expression_data.csv \
    --output heatmap.png \
    --cluster \
    --cmap RdYlGn_r \
    --title "Gene Expression Heatmap"

Python API:

from pygage.visualization_utils import HeatmapPlotter, VennDiagram, ColorUtils
import polars as pl

# Heatmap
data = pl.read_csv('expression_data.csv')
plotter = HeatmapPlotter()
plotter.plot_clustered_heatmap(data, output_file='heatmap.png')

# Venn diagram
venn = VennDiagram()
counts = venn.venn_counts(data, include='both')
venn.plot_venn2(counts, ['Set1', 'Set2'], 'venn.png')

# Color palette
cmap = ColorUtils.greenred(256)

---

4. data_processing_utils.py

Data transformation, normalization, and gene extraction.

Usage:

# Normalize data
pygage-data_processing_utils.py normalize \
    --input expression_data.csv \
    --output normalized_data.csv

# Extract essential genes
pygage-data_processing_utils.py extract \
    --input expression_data.csv \
    --genes gene_list.txt \
    --output essential_genes.csv \
    --threshold 1.5

# Export and visualize
pygage-data_processing_utils.py export \
    --input expression_data.csv \
    --genes gene_list.txt \
    --output gene_data.csv \
    --heatmap gene_heatmap.png \
    --normalize

Python API:

from pygage.data_processing_utils import DataTransformer, GeneExtractor, GeneDataExporter
import polars as pl

# Normalize
data = pl.read_csv('expression_data.csv')
transformer = DataTransformer()
normalized = transformer.row_normalize(data)

# Extract essential genes
extractor = GeneExtractor()
essential = extractor.extract_essential_genes(
    gene_set=['TP53', 'BRCA1', 'EGFR'],
    expression_data=data,
    threshold=1.0
)

# Export with visualization
exporter = GeneDataExporter()
exporter.export_gene_data(
    genes=['TP53', 'BRCA1'],
    expression_data=data,
    output_file='output.csv',
    create_heatmap=True,
    heatmap_output='heatmap.png'
)

---

5. gage_core.py

Core GAGE analysis functions.

Usage:

pygage-core.py \
    --expression expression_data.csv \
    --gene-sets pathways.json \
    --gene-col gene_id \
    --ref-indices 0 1 2 \
    --samp-indices 3 4 5 \
    --comparison paired \
    --test-method t-test \
    --cutoff 0.1 \
    --output results/

Python API:

from pygage.gage_core import GAGEPreparation, GAGEAnalysis
import polars as pl
import json

# Load data
expr_data = pl.read_csv('expression_data.csv')
with open('gene_sets.json') as f:
    gene_sets = json.load(f)

# Prepare data
prep = GAGEPreparation()
prepared = prep.prepare_expression(
    expr_data,
    ref_indices=[0, 1, 2],
    samp_indices=[3, 4, 5],
    comparison='paired'
)

# Run GAGE
gage = GAGEAnalysis()
results = gage.run_gage(
    prepared,
    gene_sets,
    test_method='t-test'
)

# Filter significant
significant = gage.filter_significant(cutoff=0.1)

---

6. gage_tests.py

Statistical tests for gene set analysis.

Usage:

pygage-tests.py \
    --expression expression_data.csv \
    --gene-sets pathways.json \
    --gene-col gene_id \
    --method t-test \
    --min-size 10 \
    --max-size 500 \
    --output test_results.tsv

Python API:

from pygage.tests import GeneSetTests
import polars as pl
import json

expr_data = pl.read_csv('expression_data.csv')
with open('gene_sets.json') as f:
    gene_sets = json.load(f)

tester = GeneSetTests()

# t-test
results = tester.t_test(expr_data, gene_sets)

# z-test
results = tester.z_test(expr_data, gene_sets)

# KS test
results = tester.kolmogorov_smirnov_test(expr_data, gene_sets)

---

7. results_analysis.py

Analyze and compare GAGE results.

Usage:

# Compare multiple results
pygage-results_analysis.py compare \
    --inputs result1.tsv result2.tsv result3.tsv \
    --names "Control" "Treatment1" "Treatment2" \
    --cutoff 0.1 \
    --output combined_results.tsv \
    --venn comparison_venn.png

# Filter significant results
pygage-results_analysis.py filter \
    --greater greater_results.tsv \
    --less less_results.tsv \
    --cutoff 0.1 \
    --output-dir filtered_results/

# Group overlapping gene sets
pygage-results_analysis.py group \
    --results gage_results.tsv \
    --gene-sets pathways.json \
    --expression expression_data.csv \
    --output gene_set_groups.json

Python API:

from pygage.results_analysis import ResultsComparator, GeneSetGrouper, SignificanceFilter
from pathlib import Path

# Compare results
comparator = ResultsComparator()
combined = comparator.compare_results(
    [Path('r1.tsv'), Path('r2.tsv')],
    ['Sample1', 'Sample2'],
    q_cutoff=0.1,
    output_file=Path('combined.tsv')
)

# Create Venn diagram
comparator.create_venn_comparison(
    [Path('r1.tsv'), Path('r2.tsv')],
    ['Sample1', 'Sample2'],
    output_file=Path('venn.png')
)

# Filter significant
filterer = SignificanceFilter()
filtered = filterer.filter_significant(
    results={'greater': greater_df, 'less': less_df},
    cutoff=0.1
)

# Group gene sets
grouper = GeneSetGrouper()
groups = grouper.group_gene_sets(
    results_df,
    gene_sets,
    expression_df,
    output_file=Path('groups.json')
)

---

Complete Workflow Example

#!/bin/bash

# 1. Convert gene IDs (if needed)
pygage-gene_id_utils.py gene_list.txt \
    --mapping egSymb.csv \
    --direction eg2sym \
    --output gene_symbols.csv

# 2. Retrieve KEGG pathways
pygage-pathway_database_utils.py kegg \
    --species hsa \
    --id-type entrez \
    --output kegg_pathways.json

# 3. Prepare and normalize expression data
pygage-data_processing_utils.py normalize \
    --input raw_expression.csv \
    --output normalized_expression.csv

# 4. Run GAGE analysis
pygage-core.py \
    --expression normalized_expression.csv \
    --gene-sets kegg_pathways.json \
    --gene-col gene_id \
    --ref-indices 0 1 2 \
    --samp-indices 3 4 5 \
    --comparison paired \
    --test-method t-test \
    --cutoff 0.1 \
    --output gage_results/

# 5. Filter significant results
pygage-results_analysis.py filter \
    --greater gage_results/greater.tsv \
    --less gage_results/less.tsv \
    --cutoff 0.05 \
    --output-dir significant_results/

# 6. Create visualizations
pygage-visualization_utils.py heatmap \
    --input significant_results/greater_significant.tsv \
    --output heatmap_upregulated.png \
    --cluster \
    --title "Up-regulated Pathways"

# 7. Extract essential genes from top pathway
pygage-data_processing_utils.py extract \
    --input normalized_expression.csv \
    --genes top_pathway_genes.txt \
    --output essential_genes.csv \
    --threshold 2.0

# 8. Export with visualization
pygage-data_processing_utils.py export \
    --input normalized_expression.csv \
    --genes essential_genes.csv \
    --output essential_genes_data.csv \
    --heatmap essential_genes_heatmap.png \
    --normalize

---

Data Format Requirements

Expression Data (CSV/TSV)

gene_id,sample1,sample2,sample3,sample4,sample5,sample6
GENE001,5.2,5.4,5.1,8.3,8.5,8.1
GENE002,3.1,3.3,3.2,3.4,3.5,3.3
GENE003,7.8,7.9,8.0,4.2,4.1,4.3

Gene Sets (JSON)

{
  "pathway1": ["GENE001", "GENE002", "GENE005"],
  "pathway2": ["GENE003", "GENE004", "GENE006"],
  "pathway3": ["GENE001", "GENE003", "GENE007"]
}

Or with metadata:

{
  "gene_sets": {
    "pathway1": ["GENE001", "GENE002"],
    "pathway2": ["GENE003", "GENE004"]
  },
  "pathway_names": {
    "pathway1": "Cell cycle regulation",
    "pathway2": "DNA repair"
  }
}

Gene ID Mapping (CSV/TSV)

entrez_id,symbol
1,TP53
2,BRCA1
3,EGFR

---

Key Differences from R Version

1. Polars instead of Pandas

• Faster performance
• More intuitive API
• Better memory efficiency
• Lazy evaluation support

# Polars syntax
df.filter(pl.col('value') > 0.5)
df.select(['col1', 'col2'])
df.join(other_df, on='key', how='left')

2. Seaborn/Matplotlib instead of base R graphics

• More modern visualizations
• Better default aesthetics
• Easier customization

3. Argparse for CLI

• Subcommands for different operations
• Help text and validation built-in
• Type checking

4. No Random Seed Issues

• Random seed properly handled by scipy
• No hardcoded values

5. JSON for Gene Sets

• More portable than R's RData format
• Human-readable
• Easy to integrate with other tools

---

Error Handling

All scripts include comprehensive error handling:

try:
    converter = GeneIDConverter('mapping.csv')
    symbols = converter.eg2sym(['1', '2', '3'])
except ValueError as e:
    print(f"Error: {e}")
except FileNotFoundError:
    print("Mapping file not found")

---

Troubleshooting

Issue: "No numeric columns found"

Solution: Ensure expression data has numeric columns and correct gene ID column name

Issue: "Mapping data not loaded"

Solution: Call load_mapping() or initialize with mapping file path

Issue: "Can't create Venn diagram for more than 3 sets"

Solution: Venn diagrams limited to 2-3 sets; use heatmap for more comparisons

Issue: "Memory error with large datasets"

Solution: Use polars lazy evaluation or process in chunks

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Contributing

Improvements welcome:

1. Add more statistical tests
2. Implement additional visualizations
3. Add support for more gene set databases
4. Improve performance with parallel processing

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📄 License

Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) — See LICENSE file

Citations:

If you are publishing results obtained using PyGAGE, please cite:

• Pre-Print PyGAGE: Figueroa III JL, Brouwer CR, White III RA. 2026. Statistically resolving gene-set enrichment for pathway analysis that is broadly applicable via PyGAGE. bioRxiv.

If you using the R version please cite:

• Luo, W., Friedman, M. S., Shedden, K., Hankenson, K. D., & Woolf, P. J. (2009). GAGE: generally applicable gene set enrichment for pathway analysis. BMC Bioinformatics, 10, 161. GAGE

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Contributing to PyGAGE

We welcome contributions of other experts expanding features in PyGAGE including the R and python versions. Please contact us via support.

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📞 Support

• Issues: open an issue.
• Email: Dr. Richard Allen White III

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