Workflow for enrichment testing, ranked-gene analysis, pathway scoring, and pathway-focused visualization across omics outputs.
Scanned 9/4/2026
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---
name: pathway-analysis
description: Workflow for enrichment testing, ranked-gene analysis, pathway scoring, and pathway-focused visualization across omics outputs.
tool_type: python
primary_tool: Reactome
---
# Pathway Analysis
## Version Compatibility
Reference examples assume recent stable releases of the preferred tools, especially `Reactome` and the other tools listed below.
Before using code or command patterns, verify installed versions match the environment:
- Python: `python -c "import <module>; print(<module>.__version__)"`
- CLI: `<tool> --version`
- If signatures differ, inspect the installed help or API and adapt the pattern instead of retrying unchanged.
## Overview
Workflow for enrichment testing, ranked-gene analysis, pathway scoring, and pathway-focused visualization across omics outputs.
## When To Use This Skill
- use when the task is pathway enrichment or gene set interpretation
- use when the user has gene lists, ranked statistics, or pathway-scored samples
- use when Reactome, KEGG, GO, or similar resources are part of the deliverable
## Quick Route
- If the input is raw or minimally processed data, start with validation and QC before any modeling.
- If the input is already processed, skip directly to the first workflow step that matches the user goal.
- If the user asks for a biological conclusion, always produce at least one QC or confidence artifact alongside the final result.
## Progressive Disclosure
- Read `references/technical_reference.md` when you need deeper tool-selection rules, environment adaptation notes, or extra validation guidance.
- Keep `SKILL.md` as the main execution path and load the reference file only when the task or failure mode needs the extra detail.
## Default Rules
- Prefer Python-first workflows unless the task explicitly requires something else.
- Keep intermediate and final outputs separated.
- Record software versions, reference builds, and key parameters when they affect interpretation.
- Favor reproducible tables and figures over one-off interactive-only outputs.
## Expected Inputs
- gene lists or ranked statistics
- pathway databases
- optional sample-level matrices
## Expected Outputs
- enriched pathway tables
- pathway plots
- pathway interpretation summaries
## Preferred Tools
- Reactome and STRING resources
- pandas
- matplotlib
- seaborn
## Starter Pattern
```text
Preferred starting point: Reactome
Inputs: gene lists or ranked statistics, pathway databases, optional sample-level matrices
Outputs: enriched pathway tables, pathway plots, pathway interpretation summaries
```
## Workflow
### 1. Choose enrichment mode
Use over-representation for filtered gene lists and ranked methods for full signed statistics.
### 2. Match identifiers
Standardize gene IDs to the pathway database before testing.
### 3. Run enrichment and summarize
Report effect direction, significance, and pathway sizes.
### 4. Visualize selectively
Use dot plots, bar plots, or network summaries without overwhelming the reader.
### 5. Export pathway-ready tables
Save standardized pathway identifiers, scores, and member genes.
## Output Artifacts
- Recommended output layout:
- `results/` for final tables and serialized objects
- `figures/` for plots and static visual exports
- `qc/` for checks that justify downstream interpretation
- Minimum expected outputs for this skill:
- `enriched pathway tables`
- `pathway plots`
- `pathway interpretation summaries`
## Quality Review
- Confirm identifiers and metadata join correctly before modeling or summarizing.
- Generate at least one QC artifact before final biological interpretation.
- Keep raw or minimally processed inputs separate from transformed outputs.
- Verify that modalities, samples, and model assumptions align before integration or inference.
- Export factors, scores, or model outputs together with interpretation context.
## Anti-Patterns
- mixing identifier systems without conversion
- treating pathway databases as interchangeable without stating the source
- showing only p-values without effect direction or gene overlap context
## Related Skills
- `Multi-Omics Integration`
- `Systems Biology`
- `Causal Genomics`
- `Machine Learning For Omics`
## Optional Supplements
- `reactome-database`
- `string-database`
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