Ensembl Database
"Query Ensembl genome database REST API for 250+ species. Gene lookups, sequence retrieval, variant analysis, comparative genomics, orthologs, VEP predictions, for genomic research."
$ npx claude-code-templates@latest --skill="scientific/ensembl-database" --yesRequires Claude Code. The command adds this skill to your project's .claudedirectory — nothing runs on ToolZip's servers.
What's inside this skill
Component source
Ensembl Database
Overview
Access and query the Ensembl genome database, a comprehensive resource for vertebrate genomic data maintained by EMBL-EBI. The database provides gene annotations, sequences, variants, regulatory information, and comparative genomics data for over 250 species. Current release is 115 (September 2025).
When to Use This Skill
This skill should be used when:
- Querying gene information by symbol or Ensembl ID
- Retrieving DNA, transcript, or protein sequences
- Analyzing genetic variants using the Variant Effect Predictor (VEP)
- Finding orthologs and paralogs across species
- Accessing regulatory features and genomic annotations
- Converting coordinates between genome assemblies (e.g., GRCh37 to GRCh38)
- Performing comparative genomics analyses
- Integrating Ensembl data into genomic research pipelines
Core Capabilities
1. Gene Information Retrieval
Query gene data by symbol, Ensembl ID, or external database identifiers.
Common operations:- Look up gene information by symbol (e.g., "BRCA2", "TP53")
- Retrieve transcript and protein information
- Get gene coordinates and chromosomal locations
- Access cross-references to external databases (UniProt, RefSeq, etc.)
from ensembl_rest import EnsemblClient
client = EnsemblClient()
# Look up gene by symbol
gene_data = client.symbol_lookup(
species='human',
symbol='BRCA2'
)
# Get detailed gene information
gene_info = client.lookup_id(
id='ENSG00000139618', # BRCA2 Ensembl ID
expand=True
)
Direct REST API (no package):
import requests
server = "https://rest.ensembl.org"
# Symbol lookup
response = requests.get(
f"{server}/lookup/symbol/homo_sapiens/BRCA2",
headers={"Content-Type": "application/json"}
)
gene_data = response.json()
2. Sequence Retrieval
Fetch genomic, transcript, or protein sequences in various formats (JSON, FASTA, plain text).
Operations:- Get DNA sequences for genes or genomic regions
- Retrieve transcript sequences (cDNA)
- Access protein sequences
- Extract sequences with flanking regions or modifications
# Using ensembl_rest package
sequence = client.sequence_id(
id='ENSG00000139618', # Gene ID
content_type='application/json'
)
# Get sequence for a genomic region
region_seq = client.sequence_region(
species='human',
region='7:140424943-140624564' # chromosome:start-end
)
3. Variant Analysis
Query genetic variation data and predict variant consequences using the Variant Effect Predictor (VEP).
Capabilities:- Look up variants by rsID or genomic coordinates
- Predict functional consequences of variants
- Access population frequency data
- Retrieve phenotype associations
# Predict variant consequences
vep_result = client.vep_hgvs(
species='human',
hgvs_notation='ENST00000380152.7:c.803C>T'
)
# Query variant by rsID
variant = client.variation_id(
species='human',
id='rs699'
)
4. Comparative Genomics
Perform cross-species comparisons to identify orthologs, paralogs, and evolutionary relationships.
Operations:- Find orthologs (same gene in different species)
- Identify paralogs (related genes in same species)
- Access gene trees showing evolutionary relationships
- Retrieve gene family information
# Find orthologs for a human gene
orthologs = client.homology_ensemblgene(
id='ENSG00000139618', # Human BRCA2
target_species='mouse'
)
# Get gene tree
gene_tree = client.genetree_member_symbol(
species='human',
symbol='BRCA2'
)
5. Genomic Region Analysis
Find all genomic features (genes, transcripts, regulatory elements) in a specific region.
Use cases:- Identify all genes in a chromosomal region
- Find regulatory features (promoters, enhancers)
- Locate variants within a region
- Retrieve structural features
# Find all features in a region
features = client.overlap_region(
species='human',
region='7:140424943-140624564',
feature='gene'
)
6. Assembly Mapping
Convert coordinates between different genome assemblies (e.g., GRCh37 to GRCh38).
Important: Usehttps://grch37.rest.ensembl.org for GRCh37/hg19 queries and https://rest.ensembl.org for current assemblies.
Example:
from ensembl_rest import AssemblyMapper
# Map coordinates from GRCh37 to GRCh38
mapper = AssemblyMapper(
species='human',
asm_from='GRCh37',
asm_to='GRCh38'
)
mapped = mapper.map(chrom='7', start=140453136, end=140453136)
API Best Practices
Rate Limiting
The Ensembl REST API has rate limits. Follow these practices:
- Respect rate limits: Maximum 15 requests per second for anonymous users
- Handle 429 responses: When rate-limited, check the
Retry-Afterheader and wait - Use batch endpoints: When querying multiple items, use batch endpoints where available
- Cache results: Store frequently accessed data to reduce API calls
Error Handling
Always implement proper error handling:
import requests
import time
def query_ensembl(endpoint, params=None, max_retries=3):
server = "https://rest.ensembl.org"
headers = {"Content-Type": "application/json"}
for attempt in range(max_retries):
response = requests.get(
f"{server}{endpoint}",
headers=headers,
params=params
)
if response.status_code == 200:
return response.json()
elif response.status_code == 429:
# Rate limited - wait and retry
retry_after = int(response.headers.get('Retry-After', 1))
time.sleep(retry_after)
else:
response.raise_for_status()
raise Exception(f"Failed after {max_retries} attempts")
Installation
Python Package (Recommended)
uv pip install ensembl_rest
The ensembl_rest package provides a Pythonic interface to all Ensembl REST API endpoints.
Direct REST API
No installation needed - use standard HTTP libraries like requests:
uv pip install requests
Resources
references/
api_endpoints.md: Comprehensive documentation of all 17 API endpoint categories with examples and parameters
scripts/
ensembl_query.py: Reusable Python script for common Ensembl queries with built-in rate limiting and error handling
Common Workflows
Workflow 1: Gene Annotation Pipeline
- Look up gene by symbol to get Ensembl ID
- Retrieve transcript information
- Get protein sequences for all transcripts
- Find orthologs in other species
- Export results
Workflow 2: Variant Analysis
- Query variant by rsID or coordinates
- Use VEP to predict functional consequences
- Check population frequencies
- Retrieve phenotype associations
- Generate report
Workflow 3: Comparative Analysis
- Start with gene of interest in reference species
- Find orthologs in target species
- Retrieve sequences for all orthologs
- Compare gene structures and features
- Analyze evolutionary conservation
Species and Assembly Information
To query available species and assemblies:
# List all available species
species_list = client.info_species()
# Get assembly information for a species
assembly_info = client.info_assembly(species='human')
Common species identifiers:
- Human:
homo_sapiensorhuman - Mouse:
mus_musculusormouse - Zebrafish:
danio_rerioorzebrafish - Fruit fly:
drosophila_melanogaster
Additional Resources
- Official Documentation: https://rest.ensembl.org/documentation
- Python Package Docs: https://ensemblrest.readthedocs.io
- EBI Training: https://www.ebi.ac.uk/training/online/courses/ensembl-rest-api/
- Ensembl Browser: https://useast.ensembl.org
- GitHub Examples: https://github.com/Ensembl/ensembl-rest/wiki
Related Claude Code Skills
Generate Image
Generate or edit images using AI models (FLUX, Gemini). Use for general-purpose image generation including photos, illustrations, artwork, visual assets, concept art, and any image that isn't a technical diagram or schematic. For flowcharts, circuits, pathways, and technical diagrams, use the scientific-schematics skill instead.
Markitdown
"Convert files and office documents to Markdown. Supports PDF, DOCX, PPTX, XLSX, images (with OCR), audio (with transcription), HTML, CSV, JSON, XML, ZIP, YouTube URLs, EPubs and more."
Scientific Critical Thinking
"Evaluate research rigor. Assess methodology, experimental design, statistical validity, biases, confounding, evidence quality (GRADE, Cochrane ROB), for critical analysis of scientific claims."
Scientific Slides
"Build slide decks and presentations for research talks. Use this for making PowerPoint slides, conference presentations, seminar talks, research presentations, thesis defense slides, or any scientific talk. Provides slide structure, design templates, timing guidance, and visual validation. Works with PowerPoint and LaTeX Beamer."
Statistical Analysis
"Statistical analysis toolkit. Hypothesis tests (t-test, ANOVA, chi-square), regression, correlation, Bayesian stats, power analysis, assumption checks, APA reporting, for academic research."
Market Research Reports
"Generate comprehensive market research reports (50+ pages) in the style of top consulting firms (McKinsey, BCG, Gartner). Features professional LaTeX formatting, extensive visual generation with scientific-schematics and generate-image, deep integration with research-lookup for data gathering, and multi-framework strategic analysis including Porter's Five Forces, PESTLE, SWOT, TAM/SAM/SOM, and BCG Matrix."
Catalog data and component content are sourced from the open-source davila7/claude-code-templates project (MIT license). ToolZip curates the listing and writes original descriptions; every component links back to its original source. Claude Code is a product of Anthropic. ToolZip is an independent catalog and is not affiliated with or endorsed by Anthropic.