Query ensembl
Skill BioTender-max/awesome-bio-agent-skills/skills/bioclaw/query-ensembl
Query Ensembl for genomic data. Use when user asks about gene coordinates, genomic sequences, variants, gene structure, exons, transcripts, or species comparison. Triggers on "ensembl", "gene coordinates", "genomic location", "exon", "transcript", "variant location", "rsid", "rs number".From its SKILL.md
npx -y skills add BioTender-max/awesome-bio-agent-skills --skill query-ensemblAssembled from the repository path, not quoted from the project. Check it against their README if it does not work.
One thing to look at
- no licenseNo license file was found in the repository. Code published without one is not open source by default, so using it at work is a question for whoever answers licensing questions where you are.
SKILL.md
3.3 KB, 832 tokens by cl100k_base, as published. Nobody here has run it
Ensembl REST API Query
Query the Ensembl REST API for genomic annotations, sequences, and variants.
When to Use
- User asks about a gene's genomic location, exons, or transcripts
- User wants to look up an rsID or variant
- User needs genomic/cDNA/protein sequences
- User asks about gene structure or regulatory features
- User wants cross-species gene information
How to Execute
import requests
import json
BASE_URL = "https://rest.ensembl.org"
HEADERS = {"Content-Type": "application/json", "Accept": "application/json"}
# 1. Gene lookup by symbol
def lookup_gene(symbol, species="homo_sapiens"):
url = f"{BASE_URL}/lookup/symbol/{species}/{symbol}"
r = requests.get(url, headers=HEADERS, params={"expand": 1})
r.raise_for_status()
return r.json()
# 2. Get sequence
def get_sequence(ensembl_id, seq_type="genomic"):
url = f"{BASE_URL}/sequence/id/{ensembl_id}"
r = requests.get(url, headers=HEADERS, params={"type": seq_type})
r.raise_for_status()
return r.json()
# 3. Variant lookup by rsID
def lookup_variant(rsid, species="homo_sapiens"):
url = f"{BASE_URL}/variation/{species}/{rsid}"
r = requests.get(url, headers=HEADERS)
r.raise_for_status()
return r.json()
# 4. Get overlapping features in a region
def overlap_region(species, chrom, start, end, feature="gene"):
url = f"{BASE_URL}/overlap/region/{species}/{chrom}:{start}-{end}"
r = requests.get(url, headers=HEADERS, params={"feature": feature})
r.raise_for_status()
return r.json()
# 5. Cross-species homologs
def get_homologs(ensembl_id, target_species=None):
url = f"{BASE_URL}/homology/id/{ensembl_id}"
params = {}
if target_species:
params["target_species"] = target_species
r = requests.get(url, headers=HEADERS, params=params)
r.raise_for_status()
return r.json()
# Example: look up BRCA2
gene = lookup_gene("BRCA2")
print(f"Gene: {gene['display_name']}")
print(f"Ensembl ID: {gene['id']}")
print(f"Location: chr{gene['seq_region_name']}:{gene['start']}-{gene['end']}")
print(f"Strand: {'+' if gene['strand'] == 1 else '-'}")
print(f"Biotype: {gene['biotype']}")
print(f"Description: {gene.get('description', 'N/A')}")
Key Endpoints
| Endpoint | Use |
|---|---|
/lookup/symbol/{species}/{symbol} | Gene info by symbol |
/lookup/id/{id} | Info by Ensembl ID |
/sequence/id/{id}?type=genomic | Get sequence |
/variation/{species}/{rsid} | Variant info |
/overlap/region/{species}/{chr}:{start}-{end} | Features in region |
/homology/id/{id} | Orthologs/paralogs |
/vep/{species}/hgvs/{hgvs} | Variant effect prediction |
Notes
- Region queries max 4,900,000 bp
- Species:
homo_sapiens,mus_musculus,danio_rerio,drosophila_melanogaster - Always use
application/jsonAccept header
Follow-up Suggestions
- "Want me to get the protein sequence for this gene?"
- "Should I check for known pathogenic variants?"
- "Want me to find orthologs in mouse?"
What ships with it
Read from the repository
Just SKILL.md. No reference files, no scripts.