生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
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Pull pre-computed ortholog calls from public databases (OrthoDB, Ensembl Compara, OMA browser, eggNOG, PANTHER, KEGG Orthology, HomoloGene) via their REST APIs. Use when orthologs are already curated upstream, when the question is "what is the X ortholog of Y" rather than "how to infer orthology de novo", when batch-mapping gene IDs across species, or when comparing the resources for consensus calls. Encodes confidence-level semantics, 1:1 vs 1:many vs many:many, HomoloGene deprecation, and when to defect to de novo computation.
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Reference examples tested with: requests 2.31+, pandas 2.2+; OrthoDB v12 API, Ensembl REST (Ensembl release 112+), OMA REST API, eggNOG 6.0+, PANTHER v18+
Before using code patterns, verify installed versions match. If versions differ:
pip show requests pandasIf endpoints return 404 or unexpected JSON, check release notes for the resource; schema migrations happen with each major version (Ensembl release is the biggest moving target).
"What is the X ortholog of gene Y?" -> Many ortholog resources have already done the inference at scale. Pulling their answers is faster and often more reliable than re-computing. This skill is the database-access view: how to query the major orthology resources programmatically, what their confidence semantics mean, and when their disagreements matter.
For de novo orthology inference (running OrthoFinder, SonicParanoid, OMA standalone on local proteomes), see comparative-genomics/ortholog-inference — that's a much deeper treatment of the computational side.
This skill is about pulling answers from:
OrthoDB v12 — broadest coverage (1700+ species), levels from species-specific to deep
Ensembl Compara — vertebrate-focused, tree-reconciled, confidence scores
OMA browser — high precision, HOG (Hierarchical Orthologous Group) framework
eggNOG 6.0 — pre-computed functional groups, deepest functional annotation
PANTHER — protein family + ortholog calls with experimentally validated curation
KEGG Orthology (KO) — pathway-centric orthologous functional units
HomoloGene — deprecated since 2014, but data still queryable for legacy comparison
Python: requests.get() against REST endpoints; pandas for parsing
CLI: curl against the same endpoints; OrthoDB also has bulk downloads
import requests
import pandas as pd
import time
No API keys required for any of these resources (as of 2026), but rate limits apply — see per-resource notes below.
| Question | Resource | Why |
|---|---|---|
| Ortholog of human gene X in mouse | Ensembl Compara | Best-curated for vertebrates; confidence score per call |
| Ortholog of gene X across all 1700+ species | OrthoDB | Broadest taxonomic coverage |
| Single-copy orthologs for phylogenomics | OrthoDB at species-tree level | Pre-computed; large taxonomic groups |
| Functional annotation transfer | eggNOG-mapper or eggNOG API | OG-based functional categories |
| Pathway-centric orthology (KEGG pathways) | KEGG Orthology (KO) | KO IDs link directly to pathway maps |
| Curated function-aware orthologs | PANTHER | Smaller scope; manually curated; experiment-supported |
| Compare resource consensus | All of them + intersect | Disagreement is itself a signal |
| Plant orthology (Ensembl Plants) | Ensembl Compara (plant division) | Better than Ensembl vertebrate for plants |
| Bacterial orthology | OrthoDB or eggNOG bactNOG | Ensembl Bacteria has limited Compara coverage |
| Custom proteomes not in any database | De novo computation | See comparative-genomics/ortholog-inference |
Base URL: https://data.orthodb.org/v12/
Key endpoints (all GET, JSON returned):
/search?query=<symbol>&species=<NCBI_taxid> — find ortholog groups by gene symbol/orthologs?id=<og_id>&species=<taxid> — get orthologs of a group at a specific level/group?id=<og_id> — full group info (sequences, evidence)/tab?query=<og_id> — tab-separated bulk dumpLevels are NCBI taxonomy IDs (e.g. 9606 = human, 40674 = Mammalia, 7742 = Vertebrata).
def orthodb_search(symbol, species_taxid=9606):
r = requests.get('https://data.orthodb.org/v12/search',
params={'query': symbol, 'species': species_taxid})
r.raise_for_status()
return r.json()['data'] # list of orthogroup IDs
Base URL: https://rest.ensembl.org/. JSON: Accept: application/json. Rate limit: 15 req/sec, 55,000 req/hour. Respect Retry-After on 429.
Key endpoints:
/homology/symbol/<species>/<symbol> — orthologs of a gene by symbol/homology/id/<ensembl_gene_id> — orthologs of a gene by Ensembl ID/lookup/symbol/<species>/<symbol> — resolve symbol to Ensembl ID first?type=orthologues to filter to orthologs only (drop paralogs)?target_species=<species> to filter to one target speciesdef ensembl_orthologs(symbol, species='human', target=None):
url = f'https://rest.ensembl.org/homology/symbol/{species}/{symbol}'
params = {'type': 'orthologues'}
if target:
params['target_species'] = target
r = requests.get(url, params=params, headers={'Accept': 'application/json'})
r.raise_for_status()
homologies = r.json()['data'][0]['homologies']
return [{
'target_species': h['target']['species'],
'target_id': h['target']['id'],
'type': h['type'], # ortholog_one2one / one2many / many2many / within_species_paralog
'confidence': h.get('confidence'), # 0/1; some calls lack this field
'identity_target': h['target'].get('perc_id'),
'identity_query': h['source'].get('perc_id'),
} for h in homologies]
Base URL: https://omabrowser.org/api/. JSON returned. No rate-limit doc but be polite.
Key endpoints:
/protein/<id>/orthologs/ — orthologs of a protein (UniProt or OMA ID)/hog/<hog_id>/ — Hierarchical Orthologous Group info/genome/<species_code>/ — list all genomes; species codes are 5-letter (e.g. HUMAN, MOUSE)def oma_orthologs(uniprot_acc):
r = requests.get(f'https://omabrowser.org/api/protein/{uniprot_acc}/orthologs/')
r.raise_for_status()
return r.json() # list of ortholog dicts with omaid, canonicalid, taxonId
Base URL: http://eggnog6.embl.de/api/ (web API; lighter than running eggNOG-mapper). Most heavy lifting still uses eggNOG-mapper locally (Cantalapiedra et al. 2021 Mol Biol Evol 38:5825) — for batch protein-set annotation, mapper > API.
For ad hoc lookup: search the eggNOG web interface for an orthogroup ID, then download the member set.
Base URL: https://rest.kegg.jp/. Returns plain text TSV by default (NOT JSON).
def kegg_ko_for_gene(species_code, gene):
'''KEGG species codes: hsa=human, mmu=mouse, dme=fly, etc.'''
r = requests.get(f'https://rest.kegg.jp/link/ko/{species_code}:{gene}')
r.raise_for_status()
return [line.split('\t')[1].replace('ko:', '') for line in r.text.strip().split('\n') if line]
def kegg_orthologs(ko_id):
r = requests.get(f'https://rest.kegg.jp/link/genes/{ko_id}')
return [line.split('\t')[1] for line in r.text.strip().split('\n') if line]
KEGG license: commercial use requires a paid license; academic use is free for web/API.
Base URL: http://pantherdb.org/services/oai/pantherdb/ (note the unusual base). Has a curated, smaller scope than OrthoDB but with experimental evidence.
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/efetch.fcgi?db=homologene&id=<id>&rettype=xml — still works; data frozen since 2014. Useful only for backward-compatibility with old pipelines.
Each resource defines "confidence" differently. They are NOT directly comparable.
| Resource | Confidence field | Semantics |
|---|---|---|
| Ensembl Compara | confidence 0/1 | Binary; 1 = high confidence based on gene-tree topology |
| OrthoDB | evolutionary_rate (not a confidence per se) | Inverse proxy; lower = more conserved |
| OMA | Internal QC; not exposed as a per-call score | All calls passed precision filter |
| eggNOG | Tax-level coverage | Member counts per taxonomic level |
| PANTHER | evidence codes | Experimentally validated vs predicted |
Don't average or compare confidence across resources. Use within-resource cutoffs; for cross-resource comparison, intersect call sets.
The orthology conjecture (Tatusov 1997; rigorously evaluated by Studer & Robinson-Rechavi 2009 Trends Genet 25:210; Altenhoff et al. 2012 PLoS Comput Biol 8:e1002514) — orthologs are more likely than paralogs to share function — is supported but weakly. Sub- and neo-functionalization mean a paralog can become the functional equivalent.
This is also why resources disagree. Different algorithms emphasize different evidence:
For high-stakes calls (publication, drug target choice), intersect at least two resources and inspect disagreements.
Goal: Pull Compara's high-confidence 1:1 ortholog of a single mouse gene in human.
Approach: REST query with type filter; assert 1:1; record confidence.
Reference (Ensembl REST, release 112+):
import requests
import time
def compara_one2one(symbol, source='mouse', target='human'):
url = f'https://rest.ensembl.org/homology/symbol/{source}/{symbol}'
r = requests.get(url, params={'type': 'orthologues', 'target_species': target},
headers={'Accept': 'application/json'})
if r.status_code == 429:
time.sleep(int(r.headers.get('Retry-After', '5')))
return compara_one2one(symbol, source, target)
r.raise_for_status()
hits = r.json()['data'][0]['homologies']
one2one = [h for h in hits if h['type'] == 'ortholog_one2one']
if not one2one:
return None
h = one2one[0]
return {
'source_id': h['source']['id'],
'target_id': h['target']['id'],
'confidence': h.get('confidence'),
'pid_target': h['target'].get('perc_id'),
}
Goal: Find orthologs agreed on by multiple resources to flag high-confidence calls.
Approach: Query each resource; intersect target IDs after normalizing to a common namespace (UniProt or NCBI Gene).
def cross_resource_orthologs(symbol):
'''Return target-species ortholog calls from multiple resources for cross-validation.'''
ensembl = ensembl_orthologs(symbol, species='human')
# (OMA/OrthoDB lookups omitted for brevity -- need namespace conversion via UniProt ID Mapping)
return {'ensembl': ensembl}
Goal: Build a wide table of orthologs across N species for a gene list.
Approach: Loop with rate limit; cache responses; respect Retry-After.
Reference (requests 2.31+):
def batch_ensembl_orthologs(symbols, source='human', target_species=None, sleep=0.07):
'''sleep=0.07 keeps under the 15-req/sec ceiling with margin.'''
rows = []
for sym in symbols:
try:
orthologs = ensembl_orthologs(sym, species=source, target=target_species)
for o in orthologs:
rows.append({'source_symbol': sym, **o})
except requests.HTTPError as e:
if e.response.status_code == 429:
wait = int(e.response.headers.get('Retry-After', '10'))
time.sleep(wait)
else:
rows.append({'source_symbol': sym, 'error': str(e)})
time.sleep(sleep)
return pd.DataFrame(rows)
df = batch_ensembl_orthologs(['BRCA1', 'TP53', 'MYC'], target_species='mouse')
print(df[df['type'] == 'ortholog_one2one'][['source_symbol', 'target_id', 'confidence']])
For thousands of genes, prefer Ensembl BioMart bulk export — see biomart-queries. The REST API is fine for hundreds; BioMart wins at thousands.
def oma_hog_for_protein(oma_or_uniprot_id):
r = requests.get(f'https://omabrowser.org/api/protein/{oma_or_uniprot_id}/')
r.raise_for_status()
return r.json().get('oma_hog_id')
def oma_hog_members(hog_id, level=None):
url = f'https://omabrowser.org/api/hog/{hog_id}/'
params = {'level': level} if level else {}
r = requests.get(url, params=params)
r.raise_for_status()
return r.json()
ko_ids = kegg_ko_for_gene('hsa', '7157') # human TP53
for ko in ko_ids:
orthologs = kegg_orthologs(ko)
print(f'{ko}: {len(orthologs)} orthologs across all KEGG species')
compara_one2one('MARCH1', 'human', 'mouse') -- but MARCH1 was renamed to MARCHF1 in 2020.confidence (older calls; certain species pairs).KeyError; or filter drops calls that should pass..get('confidence', None) and treat missing as unknown (not as low-confidence).comparative-genomics/ortholog-inference.| Error / symptom | Cause | Solution |
|---|---|---|
HTTPError 429 (Ensembl) | Rate limit | Sleep per Retry-After; cap at 15 req/sec |
| Empty homologies | Symbol misspelled or stale | Resolve to Ensembl ID first |
| Missing confidence field | Older calls | .get() with default |
OMA 404 | Wrong namespace (used UniProt where OMA needed OMA ID) | Use the protein lookup endpoint to resolve first |
| KEGG returns HTML | Endpoint wrong (use rest.kegg.jp) | Check URL; KEGG is text TSV not JSON |
| Resource disagreement | Different algorithms / coverage | Intersect; document choice |
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概要と使いどころ
生成图文并茂的分析报告/实验报告/质检报告(固定模版)。当用户要求"生成报告/总结报告/实验报告/质检报告/QC报告",或分析流程收尾需要交付报告时使用。报告必须基于真实分析输出,包含固定章节结构、关键指标表格和真实结果图。
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。
Predicts ADMET properties using ADMETlab 3.0 (119 endpoints with uncertainty), ADMET-AI, DeepChem MolNet, and chemprop D-MPNN with explicit handling of OECD QSAR principles, applicability domain assessment, calibration, hERG/CYP/AMES gold-standard endpoints, and PAINS / Lipinski / Ro5 / Veber / BBB druglikeness filters. Use when filtering compounds for drug-likeness, prioritizing leads by predicted safety, or building an in-house ADMET QSAR model.
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。
Trim PCR primers from aligned reads in amplicon-panel BAMs using samtools ampliconclip. Use when processing SARS-CoV-2 ARTIC, hereditary cancer panels, ctDNA hot-spot panels, or any amplicon assay where primer-derived bases would falsely confirm reference at primer footprints.
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。
Filter alignments by flags, mapping quality, and regions using samtools view and pysam. Use when extracting specific reads, removing low-quality alignments, or subsetting to target regions.
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。
Create and use BAI/CSI indices for BAM/CRAM files using samtools and pysam. Use when enabling random access to alignment files or fetching specific genomic regions.
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。
Read, write, and convert multiple sequence alignment files using Biopython Bio.AlignIO. Supports Clustal, PHYLIP, Stockholm, FASTA, Nexus, and other alignment formats for phylogenetics and conservation analysis. Use when reading, writing, or converting alignment file formats.
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。