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scientific-db-gene-database skill

/skills/scientific-db-gene-database

This skill enables rapid querying of NCBI Gene data by symbol or ID and returns annotations, GO terms, and RefSeqs for analysis.

This is most likely a fork of the gene-database skill from microck
npx playbooks add skill jackspace/claudeskillz --skill scientific-db-gene-database

Review the files below or copy the command above to add this skill to your agents.

Files (3)
SKILL.md
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---
name: gene-database
description: "Query NCBI Gene via E-utilities/Datasets API. Search by symbol/ID, retrieve gene info (RefSeqs, GO, locations, phenotypes), batch lookups, for gene annotation and functional analysis."
---

# Gene Database

## Overview

NCBI Gene is a comprehensive database integrating gene information from diverse species. It provides nomenclature, reference sequences (RefSeqs), chromosomal maps, biological pathways, genetic variations, phenotypes, and cross-references to global genomic resources.

## When to Use This Skill

This skill should be used when working with gene data including searching by gene symbol or ID, retrieving gene sequences and metadata, analyzing gene functions and pathways, or performing batch gene lookups.

## Quick Start

NCBI provides two main APIs for gene data access:

1. **E-utilities** (Traditional): Full-featured API for all Entrez databases with flexible querying
2. **NCBI Datasets API** (Newer): Optimized for gene data retrieval with simplified workflows

Choose E-utilities for complex queries and cross-database searches. Choose Datasets API for straightforward gene data retrieval with metadata and sequences in a single request.

## Common Workflows

### Search Genes by Symbol or Name

To search for genes by symbol or name across organisms:

1. Use the `scripts/query_gene.py` script with E-utilities ESearch
2. Specify the gene symbol and organism (e.g., "BRCA1 in human")
3. The script returns matching Gene IDs

Example query patterns:
- Gene symbol: `insulin[gene name] AND human[organism]`
- Gene with disease: `dystrophin[gene name] AND muscular dystrophy[disease]`
- Chromosome location: `human[organism] AND 17q21[chromosome]`

### Retrieve Gene Information by ID

To fetch detailed information for known Gene IDs:

1. Use `scripts/fetch_gene_data.py` with the Datasets API for comprehensive data
2. Alternatively, use `scripts/query_gene.py` with E-utilities EFetch for specific formats
3. Specify desired output format (JSON, XML, or text)

The Datasets API returns:
- Gene nomenclature and aliases
- Reference sequences (RefSeqs) for transcripts and proteins
- Chromosomal location and mapping
- Gene Ontology (GO) annotations
- Associated publications

### Batch Gene Lookups

For multiple genes simultaneously:

1. Use `scripts/batch_gene_lookup.py` for efficient batch processing
2. Provide a list of gene symbols or IDs
3. Specify the organism for symbol-based queries
4. The script handles rate limiting automatically (10 requests/second with API key)

This workflow is useful for:
- Validating gene lists
- Retrieving metadata for gene panels
- Cross-referencing gene identifiers
- Building gene annotation tables

### Search by Biological Context

To find genes associated with specific biological functions or phenotypes:

1. Use E-utilities with Gene Ontology (GO) terms or phenotype keywords
2. Query by pathway names or disease associations
3. Filter by organism, chromosome, or other attributes

Example searches:
- By GO term: `GO:0006915[biological process]` (apoptosis)
- By phenotype: `diabetes[phenotype] AND mouse[organism]`
- By pathway: `insulin signaling pathway[pathway]`

### API Access Patterns

**Rate Limits:**
- Without API key: 3 requests/second for E-utilities, 5 requests/second for Datasets API
- With API key: 10 requests/second for both APIs

**Authentication:**
Register for a free NCBI API key at https://www.ncbi.nlm.nih.gov/account/ to increase rate limits.

**Error Handling:**
Both APIs return standard HTTP status codes. Common errors include:
- 400: Malformed query or invalid parameters
- 429: Rate limit exceeded
- 404: Gene ID not found

Retry failed requests with exponential backoff.

## Script Usage

### query_gene.py

Query NCBI Gene using E-utilities (ESearch, ESummary, EFetch).

```bash
python scripts/query_gene.py --search "BRCA1" --organism "human"
python scripts/query_gene.py --id 672 --format json
python scripts/query_gene.py --search "insulin[gene] AND diabetes[disease]"
```

### fetch_gene_data.py

Fetch comprehensive gene data using NCBI Datasets API.

```bash
python scripts/fetch_gene_data.py --gene-id 672
python scripts/fetch_gene_data.py --symbol BRCA1 --taxon human
python scripts/fetch_gene_data.py --symbol TP53 --taxon "Homo sapiens" --output json
```

### batch_gene_lookup.py

Process multiple gene queries efficiently.

```bash
python scripts/batch_gene_lookup.py --file gene_list.txt --organism human
python scripts/batch_gene_lookup.py --ids 672,7157,5594 --output results.json
```

## API References

For detailed API documentation including endpoints, parameters, response formats, and examples, refer to:

- `references/api_reference.md` - Comprehensive API documentation for E-utilities and Datasets API
- `references/common_workflows.md` - Additional examples and use case patterns

Search these references when needing specific API endpoint details, parameter options, or response structure information.

## Data Formats

NCBI Gene data can be retrieved in multiple formats:

- **JSON**: Structured data ideal for programmatic processing
- **XML**: Detailed hierarchical format with full metadata
- **GenBank**: Sequence data with annotations
- **FASTA**: Sequence data only
- **Text**: Human-readable summaries

Choose JSON for modern applications, XML for legacy systems requiring detailed metadata, and FASTA for sequence analysis workflows.

## Best Practices

1. **Always specify organism** when searching by gene symbol to avoid ambiguity
2. **Use Gene IDs** for precise lookups when available
3. **Batch requests** when working with multiple genes to minimize API calls
4. **Cache results** locally to reduce redundant queries
5. **Include API key** in scripts for higher rate limits
6. **Handle errors gracefully** with retry logic for transient failures
7. **Validate gene symbols** before batch processing to catch typos

## Resources

This skill includes:

### scripts/
- `query_gene.py` - Query genes using E-utilities (ESearch, ESummary, EFetch)
- `fetch_gene_data.py` - Fetch gene data using NCBI Datasets API
- `batch_gene_lookup.py` - Handle multiple gene queries efficiently

### references/
- `api_reference.md` - Detailed API documentation for both E-utilities and Datasets API
- `common_workflows.md` - Examples of common gene queries and use cases

Overview

This skill provides programmatic access to NCBI Gene via Entrez E-utilities and the NCBI Datasets API for searching by gene symbol or ID and retrieving rich gene metadata. It supports single and batch lookups, returns RefSeqs, GO annotations, chromosomal locations, phenotypes and publication links, and is designed for gene annotation and functional analysis pipelines. Use it to validate gene lists, enrich panels with metadata, or fetch sequences for downstream analysis.

How this skill works

The skill uses E-utilities (ESearch/ESummary/EFetch) for flexible queries and cross-database searches, and the Datasets API for consolidated gene metadata and sequence retrieval. Scripts accept gene symbols or NCBI Gene IDs, optional organism/taxon filters, and support JSON, XML, FASTA and GenBank outputs. Batch processing includes built-in rate-limit handling and retry logic to manage API quotas.

When to use it

  • Searching genes by symbol or name across organisms
  • Fetching full gene records (nomenclature, RefSeqs, GO, locations) by Gene ID
  • Performing batch validation or annotation of gene lists
  • Retrieving sequences for transcript/protein-level analyses
  • Filtering genes by GO terms, phenotypes, pathways, or chromosomal regions

Best practices

  • Always provide organism/taxon when searching by symbol to avoid ambiguous matches
  • Prefer NCBI Gene IDs for precise lookups when available
  • Batch requests and local caching to reduce API usage and improve throughput
  • Include an NCBI API key to increase rate limits and reliability
  • Implement exponential backoff and retry for transient HTTP errors
  • Validate and normalize input gene symbols before batch processing

Example use cases

  • Validate and map a differential-expression gene list to NCBI Gene IDs and RefSeq accessions
  • Build an annotated gene panel with GO terms, chromosomal locations and known phenotypes
  • Download transcript and protein FASTA sequences for a set of genes for alignment or downstream tools
  • Search for genes linked to a pathway or phenotype (e.g., apoptosis or diabetes) across multiple species
  • Bulk-convert mixed identifiers (symbols, aliases, IDs) into unified Gene IDs and JSON metadata

FAQ

Which API should I use for complex searches vs. simple retrieval?

Use E-utilities for complex queries, cross-database searches, and advanced filters. Use the Datasets API for straightforward retrieval of gene metadata and sequences in a single call.

What are the rate limits and how do I increase them?

Default rate limits are lower without an API key (E-utilities ~3 req/s, Datasets ~5 req/s). Register for a free NCBI API key to raise limits to ~10 req/s and include it in requests.