Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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。
Query the Ensembl REST API for gene/transcript/protein lookup, sequence retrieval, comparative genomics (Compara), variant effect prediction (VEP), regulatory features, and cross-species ortholog/paralog calls. Use when pulling Ensembl-native data (Ensembl Gene IDs, version-pinned releases, archive endpoints for reproducibility), gene/transcript/exon structure with stable IDs, or VEP for variant annotation. Encodes the 15 req/sec rate limit, archive (e110.rest.ensembl.org) for reproducibility, Ensembl divisions (vertebrates / plants / fungi / metazoa / bacteria), and the symbol-vs-ID stability problem.
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Reference examples tested with: requests 2.31+, Ensembl REST API (release 110+); Ensembl release schedule is roughly quarterly
Before using code patterns, verify installed versions match. If versions differ:
pip show requestsEach Ensembl release has an archive REST endpoint (e.g. https://e110.rest.ensembl.org) for reproducibility.
"Pull Ensembl-native gene / transcript / variant data programmatically" -> Ensembl REST is distinct from NCBI Entrez and BioMart. It is the right answer for: stable Ensembl IDs, transcript / exon structure, VEP (Variant Effect Predictor) annotation, Compara orthologs at vertebrate scale, regulatory feature annotation, and any workflow rooted in Ensembl's coordinate system.
Two facts dominate Ensembl REST work: (1) the 15 req/sec / 55,000 req/hour rate limit — high enough for hundreds of queries, low enough that bulk work (>5,000) belongs in BioMart instead; (2) versioned archive endpoints — https://e110.rest.ensembl.org pins to release 110 for reproducibility, while https://rest.ensembl.org follows the current release.
requests.get('https://rest.ensembl.org/...')biomaRt for bulk (see biomart-queries); REST via httrimport requests
import time
BASE = 'https://rest.ensembl.org'
HEADERS = {'Accept': 'application/json'}
SLEEP = 0.07 # 15 req/sec ceiling
No API key required. Respect Retry-After header on 429.
Ensembl is divided by clade. Different REST hosts:
| Division | Host | Scope |
|---|---|---|
| Vertebrates | https://rest.ensembl.org | Human, mouse, fish, etc. (the "main" Ensembl) |
| Plants | https://rest.ensembl.org (plants division also accessible) | Arabidopsis, rice, etc. via Ensembl Genomes |
| Fungi | https://rest.ensemblgenomes.org | Yeasts, Aspergillus, etc. |
| Metazoa | https://rest.ensemblgenomes.org | Insects, nematodes, etc. |
| Bacteria | https://rest.ensemblgenomes.org | Limited (most bacteria in NCBI) |
For non-vertebrate work, check ensemblgenomes.org mirrors. As of 2024, Ensembl Genomes was being consolidated; check current host.
| URL | Behavior |
|---|---|
https://rest.ensembl.org | Current release (rolling) |
https://e110.rest.ensembl.org | Pinned to release 110 |
https://e111.rest.ensembl.org | Pinned to release 111 |
https://grch37.rest.ensembl.org | Pinned to GRCh37 (legacy assembly) |
For any published analysis, pin the release. Ensembl releases change gene model versions, exon coordinates, and transcript annotations — re-running a pipeline a year later against the live endpoint may produce different results.
| Group | Example | Purpose |
|---|---|---|
| Lookup | /lookup/symbol/human/BRCA1 | Resolve symbol or ID to stable record |
| Sequence | /sequence/id/{id} | DNA/protein sequence for ID |
| Cross References | /xrefs/symbol/human/BRCA1 | Cross-refs to other DBs |
| Homology / Compara | /homology/symbol/human/BRCA1 | Orthologs and paralogs |
| Gene Tree | /genetree/id/{tree_id} | Compara gene tree |
| VEP | /vep/human/region/{region}/{allele} | Variant effect prediction |
| Overlap | /overlap/id/{id} or /overlap/region/{region} | Genes/regulatory in interval |
| Regulatory | /regulatory/species/{species}/feature/{id} | Regulatory features |
| Variant | /variation/{species}/{id} | dbSNP / 1000G / ClinVar via Ensembl |
| LD | /ld/{species}/pairwise/{var1}/{var2} | LD between variants |
| GA4GH | /ga4gh/... | GA4GH-compliant subset |
Full reference: https://rest.ensembl.org (interactive).
Gene symbols are unstable (MARCH1 -> MARCHF1 in 2020 due to Excel autocorrect; SEPT* family also renamed). Ensembl Gene IDs (ENSG...) are stable across releases when the gene model is preserved.
Best practice:
/lookup/symbol/{species}/{symbol}.Symbol-based endpoints are convenient for interactive use; ID-based endpoints are for reproducible pipelines.
| Limit | Value |
|---|---|
| Burst | 15 req/sec |
| Hourly | 55,000 req/hour |
| Concurrent | Not enforced; courtesy 1-2 |
Respect Retry-After header on HTTP 429. For >5,000 queries, switch to BioMart bulk export (see biomart-queries) — BioMart has separate, more permissive limits.
VEP via REST is the right call for ad hoc variant annotation. For batch variant annotation (>1000 variants), download VEP and run locally (variant-calling/variant-annotation skill).
REST modes:
/vep/{species}/region/{region}/{allele} — single variant by coordinate/vep/{species}/id/{variant_id} — by dbSNP / Ensembl variant ID/vep/{species}/hgvs/{hgvs_notation} — by HGVS notationVEP returns rich annotation: consequence (missense, synonymous, intron), SIFT/PolyPhen scores, gnomAD frequencies (if available), ClinVar significance.
Compara orthology calls via Ensembl REST are covered in detail in ortholog-inference (database-access view). The relevant endpoint:
/homology/symbol/{species}/{symbol} — all orthologs across Ensembl species/homology/id/{ensembl_id} — same, by ID?target_species= to restrict to one target?type=orthologues or paralogues to filterGoal: Resolve a gene symbol to its current Ensembl Gene ID once, then use the ID for all downstream queries.
Approach: /lookup/symbol/{species}/{symbol} returns the canonical record.
Reference (requests 2.31+):
import requests
import time
BASE = 'https://rest.ensembl.org'
HEADERS = {'Accept': 'application/json'}
def get_with_retry(url, params=None, max_retries=3):
for attempt in range(max_retries):
r = requests.get(url, params=params, headers=HEADERS)
if r.status_code == 429:
time.sleep(int(r.headers.get('Retry-After', '5')))
continue
r.raise_for_status()
return r
raise RuntimeError(f'Failed after {max_retries} retries')
def symbol_to_ensembl(species, symbol):
r = get_with_retry(f'{BASE}/lookup/symbol/{species}/{symbol}')
return r.json()
info = symbol_to_ensembl('human', 'BRCA1')
print(f' Ensembl Gene ID: {info["id"]}')
print(f' Biotype: {info["biotype"]}')
print(f' Chromosome: {info["seq_region_name"]}:{info["start"]}-{info["end"]}')
print(f' Strand: {info["strand"]}')
def get_sequence(ensembl_id, seq_type='cdna'):
'''seq_type: cdna, cds, protein, genomic'''
r = get_with_retry(f'{BASE}/sequence/id/{ensembl_id}',
params={'type': seq_type, 'content-type': 'application/json'})
return r.json()
prot = get_sequence('ENSG00000139618', seq_type='protein')
print(f' Length: {len(prot["seq"])} aa')
def genes_in_region(species, region):
'''region as "chr:start-end" e.g. "17:43000000-44000000".'''
r = get_with_retry(f'{BASE}/overlap/region/{species}/{region}',
params={'feature': 'gene'})
return r.json()
for g in genes_in_region('human', '17:43000000-43200000'):
print(f' {g["external_name"]:<12} {g["id"]} {g["biotype"]:<20} {g["start"]}-{g["end"]}')
Goal: Get full annotation for a variant by coordinate.
Approach: /vep/{species}/region/{region}/{allele} returns transcript consequences, SIFT/PolyPhen, frequencies.
Reference (Ensembl REST release 110+):
def vep_region(species, region, allele):
r = get_with_retry(f'{BASE}/vep/{species}/region/{region}/{allele}')
return r.json()
# BRCA1 missense variant in GRCh38 coordinates (rest.ensembl.org defaults to GRCh38);
# for GRCh37 coords use https://grch37.rest.ensembl.org instead.
results = vep_region('human', '17:43044295-43044295:1', 'A')
if results:
for tc in results[0].get('transcript_consequences', [])[:5]:
print(f' {tc["gene_symbol"]:<8} {tc["consequence_terms"]}')
if 'sift_prediction' in tc:
print(f' SIFT: {tc["sift_prediction"]} ({tc.get("sift_score", "?")})')
def orthologs(species, symbol, target_species=None):
params = {'type': 'orthologues'}
if target_species:
params['target_species'] = target_species
r = get_with_retry(f'{BASE}/homology/symbol/{species}/{symbol}', params=params)
return r.json()['data'][0]['homologies']
for o in orthologs('human', 'BRCA1', target_species='mouse'):
print(f' {o["target"]["species"]:<15} {o["target"]["id"]} type={o["type"]} confidence={o.get("confidence")}')
def batch_symbols(species, symbols):
out = {}
for sym in symbols:
try:
out[sym] = symbol_to_ensembl(species, sym)
except requests.HTTPError as e:
out[sym] = {'error': str(e)}
time.sleep(0.07) # 15 req/sec ceiling
return out
# Pin to release 110
ARCHIVE = 'https://e110.rest.ensembl.org'
r = requests.get(f'{ARCHIVE}/lookup/symbol/human/BRCA1', headers={'Accept': 'application/json'})
print(r.json()['id'])
# Re-runs against e110 in 2030 will return the same Gene ID even if the live release has moved on.
def ld_pairwise(species, var1, var2, population='1000GENOMES:phase_3:CEU'):
r = get_with_retry(f'{BASE}/ld/{species}/pairwise/{var1}/{var2}',
params={'population_name': population})
return r.json()
/lookup/symbol/human/MARCH1 after the 2020 rename.https://rest.ensembl.org a year later.https://e110.rest.ensembl.org) for reproducibility.variant-calling/variant-annotation skill); reserve REST for ad hoc <1K variants.Homo_sapiens instead of human, or arbitrary capitalization.https://rest.ensembl.org/info/species to enumerate valid names.rest.ensembl.org.rest.ensemblgenomes.org) as of 2024 (consolidation ongoing).info/divisions to confirm.| Error / symptom | Cause | Solution |
|---|---|---|
404 on symbol lookup | HGNC rename or wrong species | Resolve to Ensembl ID; check species code |
| HTTP 429 | Rate limit | Sleep per Retry-After; cap to 15 req/sec |
| Different results 6 months later | No version pinning | Use archive endpoint (eXX.rest.ensembl.org) |
404 on non-vertebrate | Wrong host division | Switch to rest.ensemblgenomes.org |
| VEP infeasible bulk | REST is per-variant | Local VEP for bulk |
| Old archive 503 | Decommissioned | Use a current archive release |
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。
概要と使いどころ
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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。
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
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。
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
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。
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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。
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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。
End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
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。