本文へ移動
cccskills
無料GitHub で公開

reactome-database

Query the Reactome database (Analysis and Content Services). Use when the user asks about pathway analysis, gene list enrichment, retrieving results by token, finding unmapped or not-found identifiers, mapping identifiers, reaction participants (inputs, outputs), pathway hierarchy (including top-level pathways), diagram export, cross-reference mapping, or searching the knowledgebase.

インストール方法を見る

含まれるファイル(4)

  • SKILL.md10.8 KB
  • references/api_reference.md4.1 KB
  • references/citation.bib2.2 KB
  • scripts/reactome_analysis.py30.5 KB

SKILL.md(原文)

インストールする前に、エージェントに与えられる指示の中身を確認できます。

Reactome Analysis & Content Service

Prerequisites

  1. uv: Read the uv skill and follow its Setup instructions to ensure uv is installed and on PATH.
  2. User Notification: If .licenses/reactome_database_LICENSE.txt does not already exist in the workspace root directory then (1) prominently notify the user to check the terms at https://reactome.org/license and https://reactome.org/cite, then (2) create the file recording the notification text and timestamp.

Overview

Reactome is a free, open-source, curated pathway database. This skill wraps both the Analysis Service (https://reactome.org/AnalysisService/) and the Content Service (https://reactome.org/ContentService/) providing pathway enrichment analysis, identifier mapping, reaction details, pathway hierarchy navigation, diagram export, cross-reference mapping, and search.

When to Use This Skill

  • Performing pathway enrichment (overrepresentation) analysis on gene/protein lists
  • Retrieving analysis results using a token from previous enrichment
  • Identifying which genes or proteins were not found in a pathway analysis
  • Analyzing gene expression data against pathway annotations
  • Mapping identifiers to Reactome entities across species
  • Retrieving reaction participants (inputs, outputs, catalysts, regulators)
  • Navigating pathway hierarchy and listing top-level pathways
  • Finding which complexes or sets contain a protein
  • Exporting pathway/reaction diagrams (PNG/SVG) with gene highlighting
  • Cross-referencing identifiers across databases (UniProt, Ensembl, etc.)
  • Searching the Reactome knowledgebase
  • Downloading analysis reports (PDF, CSV, JSON)
  • Comparing pathways across species

Common Species IDs

Reference list for common research organisms:

  • Homo sapiens
    • ID: 9606
  • Mus musculus (Mouse)
    • ID: 48892
  • Rattus norvegicus (Rat)
    • ID: 48895

Common Pathway IDs

Reference list for commonly used Reactome pathway stable IDs:

  • Cell Cycle
    • Stable ID: R-HSA-1640170
    • Notes: Top-level pathway (broad)
  • Cell Cycle, Mitotic
    • Stable ID: R-HSA-69278
    • Notes: Specific sub-pathway — use this for diagrams and drill-downs
  • Immune System
    • Stable ID: R-HSA-168256
    • Notes: Top-level pathway
  • Signal Transduction
    • Stable ID: R-HSA-162582
    • Notes: Top-level pathway
  • Gene Expression
    • Stable ID: R-HSA-74160
    • Notes: Top-level pathway
  • Programmed Cell Death
    • Stable ID: R-HSA-5357801
    • Notes: Top-level pathway

Important: When the user asks for a "Cell Cycle" diagram or analysis, prefer the specific Cell Cycle, Mitotic pathway (R-HSA-69278) unless the user explicitly requests the top-level overview. The examples throughout this document use R-HSA-69278.

Core Rules

  1. Always use --output: Every subcommand requires --output <file> to write results to a file. Never rely on stdout for large results.
  2. Default species is Homo sapiens: Use --species to override.
  3. Tokens expire after 7 days: Store tokens from analysis results to retrieve them later without re-submitting data.
  4. Use --fdr and --pvalue to filter: Enrichment results can be overwhelming. Filter with --fdr 0.05 or --pvalue 0.01 to focus on statistically significant pathways.
  5. Identifier formats: Reactome auto-detects identifiers including gene symbols (TP53), UniProt (P04637), Ensembl (ENSG00000141510), ChEBI, OMIM, EntrezGene, and many more.
  6. Handle large outputs: For commands that return large data (like species-comparison), use the --summary flag to truncate lists and avoid exceeding workspace file size limits (1MB).
  7. Notification: If this skill is used, ensure this is mentioned in the output.

Tool Execution

The CLI tool is at scripts/reactome_analysis.py. Run with uv:

uv run scripts/reactome_analysis.py <command> [options] --output /tmp/out.json

To list all available subcommands and flags, run:

uv run scripts/reactome_analysis.py --help

Use --help to verify available subcommands or flags before executing an unfamiliar command.

Feature Domains

1. Database Info

uv run scripts/reactome_analysis.py db-version --output /tmp/version.json
uv run scripts/reactome_analysis.py db-name --output /tmp/name.json

2. Single Identifier Analysis

uv run scripts/reactome_analysis.py identifier --id TP53 --output /tmp/tp53.json
uv run scripts/reactome_analysis.py identifier-projection --id TP53 --output /tmp/tp53_proj.json

3. Batch Analysis (Enrichment)

Submit a list of identifiers for overrepresentation or expression analysis:

uv run scripts/reactome_analysis.py analyze --data "TP53,BRCA1,EGFR" --output /tmp/enrich.json
uv run scripts/reactome_analysis.py analyze --file genes.txt --output /tmp/enrich.json
uv run scripts/reactome_analysis.py analyze-projection --data "TP53,BRCA1" --output /tmp/proj.json
uv run scripts/reactome_analysis.py analyze --data "TP53,BRCA1" --fdr 0.05 --output /tmp/sig.json

Common options: --page-size (alias --limit), --page (alias --offset), --sort-by, --order, --resource, --species, --fdr, --pvalue.

4. Token-Based Result Retrieval

uv run scripts/reactome_analysis.py token-result --token TOKEN --output /tmp/result.json
uv run scripts/reactome_analysis.py token-not-found --token TOKEN --output /tmp/notfound.json
uv run scripts/reactome_analysis.py token-resources --token TOKEN --output /tmp/resources.json
uv run scripts/reactome_analysis.py token-found-entities --token TOKEN --pathway R-HSA-69278 --output /tmp/found.json
uv run scripts/reactome_analysis.py token-filter-species --token TOKEN --species-filter 9606 --output /tmp/filtered.json
uv run scripts/reactome_analysis.py token-reactions-pathway --token TOKEN --pathway R-HSA-69278 --output /tmp/rxns.json

5. Download Results

uv run scripts/reactome_analysis.py download-result --token TOKEN --output /tmp/full.json
uv run scripts/reactome_analysis.py download-pathways --token TOKEN --output /tmp/pathways.csv
uv run scripts/reactome_analysis.py download-found --token TOKEN --output /tmp/found.csv
uv run scripts/reactome_analysis.py download-not-found --token TOKEN --output /tmp/notfound.csv

6. Identifier Mapping

uv run scripts/reactome_analysis.py mapping --data "TP53,BRCA1" --output /tmp/mapped.json
uv run scripts/reactome_analysis.py mapping-projection --data "TP53" --output /tmp/mapped_proj.json

7. Reaction Participants & Mechanism of Action

Retrieve the molecular participants of a reaction (inputs, outputs, catalysts):

uv run scripts/reactome_analysis.py participants --id R-HSA-6804194 --output /tmp/participants.json
uv run scripts/reactome_analysis.py participating-entities --id R-HSA-6804194 --output /tmp/entities.json

8. Complex & Set Membership

Find which complexes or sets contain a given entity:

uv run scripts/reactome_analysis.py component-of --id R-HSA-69488 --output /tmp/complexes.json

9. Pathway Hierarchy Navigation

Move up (ancestors) or down (contained events) the pathway hierarchy:

uv run scripts/reactome_analysis.py event-ancestors --id R-HSA-69278 --output /tmp/ancestors.json
uv run scripts/reactome_analysis.py contained-events --id R-HSA-69278 --output /tmp/steps.json
uv run scripts/reactome_analysis.py top-pathways --output /tmp/top.json
uv run scripts/reactome_analysis.py low-pathways --id R-HSA-69488 --output /tmp/low.json

10. Diagram Export

Export pathway or reaction diagrams as PNG/SVG, with optional gene highlighting:

uv run scripts/reactome_analysis.py diagram --id R-HSA-69278 --output /tmp/diagram.png
uv run scripts/reactome_analysis.py diagram --id R-HSA-69278 --highlight TP53 --output /tmp/highlighted.png
uv run scripts/reactome_analysis.py diagram --id R-HSA-69278 --format svg --output /tmp/diagram.svg
uv run scripts/reactome_analysis.py reaction-diagram --id R-HSA-6804194 --output /tmp/rxn.png

11. Cross-Reference Mapping

Resolve identifiers to Reactome internal IDs and cross-references:

uv run scripts/reactome_analysis.py xref-mapping --id TP53 --output /tmp/xref.json
uv run scripts/reactome_analysis.py xref-mapping-batch --data "TP53,BRCA1" --output /tmp/xrefs.json

12. Search

uv run scripts/reactome_analysis.py search --query "TP53 apoptosis" --output /tmp/results.json

13. Query Entry by ID

uv run scripts/reactome_analysis.py query --id R-HSA-69278 --output /tmp/entry.json

14. Report & Species Comparison

uv run scripts/reactome_analysis.py report --token TOKEN --output /tmp/report.pdf
uv run scripts/reactome_analysis.py species-comparison --species-id 48892 --output /tmp/species.json
# Use --summary to truncate large output and avoid workspace file size limits
uv run scripts/reactome_analysis.py species-comparison --species-id 48892 --summary --output /tmp/species.json

Recipe: Interpreting Gene Set Enrichment

A step-by-step workflow for interpreting gene set enrichment results:

  1. Submit gene list with projection to human pathways: bash uv run scripts/reactome_analysis.py analyze-projection \ --data "TP53,BRCA1,EGFR,MYC,PTEN" --fdr 0.05 --output /tmp/enrichment.json

  2. Inspect top pathways — examine pathwaysFound, top pathway names, p-values, and FDR values in the output.

  3. Drill into a pathway — get its sub-events and reaction details: bash uv run scripts/reactome_analysis.py contained-events --id R-HSA-69278 --output /tmp/steps.json uv run scripts/reactome_analysis.py participants --id <reaction_id> --output /tmp/parts.json

  4. Visualise — export a diagram with your genes highlighted: bash uv run scripts/reactome_analysis.py diagram --id R-HSA-69278 \ --highlight "TP53,BRCA1" --output /tmp/diagram.png

  5. Check hierarchy — navigate up to see broader biological context: bash uv run scripts/reactome_analysis.py event-ancestors --id R-HSA-69278 --output /tmp/ancestors.json

  6. Cross-reference — map identifiers to other databases: bash uv run scripts/reactome_analysis.py xref-mapping --id TP53 --output /tmp/xrefs.json

Reference

For detailed API endpoint documentation, see references/api_reference.md.

レビュー

まだレビューはありません。使ってみた感想をお寄せください。

同じリポジトリのスキル

概要と使いどころ

Retrieve and analyze AlphaFold predicted structures for a protein. Use when the user provides a specific UniProt Accession ID and wants structural confidence metrics (pLDDT), domain boundary analysis, or disorder assessment. Do not use if the user only has a protein name, gene name, or amino acid sequence — ask for a UniProt ID first.

日本語の概要は準備中です。原文の説明を表示しています。

google-deepmind/science-skills3,2372026年10月10日 更新

Constructs deep-links and URLs for the AlphaGenome Atlas website. Supports generating single-variant exploration links (1-based chr:pos:ref>alt), genomic locus views (1-based closed chr:start-end), candidate summary tables, and AlphaGenome reference vs. alternate predictions. Use whenever visualizing, exploring, charting, or linking genetic variants and genomic loci on the AlphaGenome Atlas, or when asked to inspect, view, or link predictions for a genomic variant.

日本語の概要は準備中です。原文の説明を表示しています。

google-deepmind/science-skills3,2372026年10月10日 更新

Analyzes genetic variant effects on gene expression (RNA-seq), chromatin accessibility (DNASE), histone marks (ChIP), and transcription factors using the AlphaGenome API. Use when the user asks about non-coding variant effects, pathogenicity, clinical significance, disease associations, functional effects, gene expression changes, splicing disruption, or regulatory effects in promoters and enhancers. Also use for resolving biological terms to tissue/cell-type ontologies (UBERON/CL) or analyzing variants in chr:pos:ref>alt format.

日本語の概要は準備中です。原文の説明を表示しています。

google-deepmind/science-skills3,2372026年10月10日 更新

Score, annotate, and analyze the functional impact of genetic variants using AlphaGenome Variant Impact (AVI) scores. Query variants in chr:pos:ref>alt format, annotate VCF/tabular callsets, perform saturation mutagenesis window scans (1-based closed chr:start-end), and extract GENCODE v46 GTF gene/exon/junction coordinates all via the AlphaGenome Atlas API.

日本語の概要は準備中です。原文の説明を表示しています。

google-deepmind/science-skills3,2372026年10月10日 更新

Query the ChEMBL database for bioactive molecules, drug targets, bioactivity data, approved drugs, and chemical structures. Use when the user asks about compounds, targets, IC50/Ki values, drug mechanisms, or structure searches.

日本語の概要は準備中です。原文の説明を表示しています。

google-deepmind/science-skills3,2372026年10月10日 更新

Query ClinicalTrials.gov via APIv2. Use when you want to search for trials by condition, drug, location, status, or phase; retrieve trial details by NCT ID; check eligibility/inclusion criteria; count trials across conditions or time periods; identify a sponsor's trial portfolio; find recruiting trials for patient matching.

日本語の概要は準備中です。原文の説明を表示しています。

google-deepmind/science-skills3,2372026年10月10日 更新

google-deepmind のスキルをすべて見る

このスキルの問題を報告する