Ensembl Database

SkillDatabases & data

This skill lets an AI agent query the Ensembl genome database through its REST API using Python. It supports gene lookups, sequence retrieval, variant analysis, comparative genomics, orthologs, and VEP predictions for genomic research across more than 250 species. The skill includes example code, rate-limiting guidance, and error handling patterns.

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Details

Instructions available. Your AI can read the instructions. Execution depends on the setup they require.

Have Python available in the environment where the agent runs.

Ensembl DatabaseStart free

What your AI can do with it

  • Look up genes by symbol or Ensembl ID
  • Retrieve DNA, transcript, and protein sequences
  • Predict variant effects with VEP
  • Find orthologs and paralogs across species
  • Convert coordinates between genome assemblies
  • Access regulatory features and genomic annotations

Getting started

  1. Have Python available in the environment where the agent runs.
  2. Install the ensembl_rest package or use the requests library to call the REST API directly.
  3. Add the skill to the agent's configuration so it can load the example code and guidance.
  4. Run a test query such as a gene symbol lookup to confirm the agent can reach the Ensembl REST API.

What this skill tells your AI

The instructions your AI receives, as published by davila7/claude-code-templates in cli-tool/components/skills/scientific/ensembl-database/SKILL.md and read by ahel’s review.

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.)

Using the ensembl_rest package:

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

Example:

# 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

VEP example:

# 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

Example:

# 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

Example:

# 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: Use https://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:

  1. Respect rate limits: Maximum 15 requests per second for anonymous users
  2. Handle 429 responses: When rate-limited, check the Retry-After header and wait
  3. Use batch endpoints: When querying multiple items, use batch endpoints where available
  4. 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

  1. Look up gene by symbol to get Ensembl ID
  2. Retrieve transcript information
  3. Get protein sequences for all transcripts
  4. Find orthologs in other species
  5. Export results

Workflow 2: Variant Analysis

  1. Query variant by rsID or coordinates
  2. Use VEP to predict functional consequences
  3. Check population frequencies
  4. Retrieve phenotype associations
  5. Generate report

Workflow 3: Comparative Analysis

  1. Start with gene of interest in reference species
  2. Find orthologs in target species
  3. Retrieve sequences for all orthologs
  4. Compare gene structures and features
  5. 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_sapiens or human
  • Mouse: mus_musculus or mouse
  • Zebrafish: danio_rerio or zebrafish
  • Fruit fly: drosophila_melanogaster

Additional Resources

Signals

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Questions

What is the current Ensembl release?
The current release is 115, dated September 2025.
How many species does Ensembl cover?
The database provides data for over 250 species.
What is VEP?
VEP stands for Variant Effect Predictor. It predicts the functional consequences of genetic variants.
Can I use this skill without installing a Python package?
Yes. The skill shows how to call the Ensembl REST API directly with the requests library, so the ensembl_rest package is optional.
Does the skill handle rate limiting?
Yes. The skill includes rate-limiting guidance and error handling patterns.
Advanced
Item type
skill
Key
ensembl-database
Source
github.com/davila7/claude-code-templates