Opentargets Database
"Query Open Targets Platform for target-disease associations, drug target discovery, tractability/safety data, genetics/omics evidence, known drugs, for therapeutic target identification."
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Open Targets Database
Overview
The Open Targets Platform is a comprehensive resource for systematic identification and prioritization of potential therapeutic drug targets. It integrates publicly available datasets including human genetics, omics, literature, and chemical data to build and score target-disease associations.
Key capabilities:- Query target (gene) annotations including tractability, safety, expression
- Search for disease-target associations with evidence scores
- Retrieve evidence from multiple data types (genetics, pathways, literature, etc.)
- Find known drugs for diseases and their mechanisms
- Access drug information including clinical trial phases and adverse events
- Evaluate target druggability and therapeutic potential
When to Use This Skill
This skill should be used when:
- Target discovery: Finding potential therapeutic targets for a disease
- Target assessment: Evaluating tractability, safety, and druggability of genes
- Evidence gathering: Retrieving supporting evidence for target-disease associations
- Drug repurposing: Identifying existing drugs that could be repurposed for new indications
- Competitive intelligence: Understanding clinical precedence and drug development landscape
- Target prioritization: Ranking targets based on genetic evidence and other data types
- Mechanism research: Investigating biological pathways and gene functions
- Biomarker discovery: Finding genes differentially expressed in disease
- Safety assessment: Identifying potential toxicity concerns for drug targets
Core Workflow
1. Search for Entities
Start by finding the identifiers for targets, diseases, or drugs of interest.
For targets (genes):from scripts.query_opentargets import search_entities
# Search by gene symbol or name
results = search_entities("BRCA1", entity_types=["target"])
# Returns: [{"id": "ENSG00000012048", "name": "BRCA1", ...}]
For diseases:
# Search by disease name
results = search_entities("alzheimer", entity_types=["disease"])
# Returns: [{"id": "EFO_0000249", "name": "Alzheimer disease", ...}]
For drugs:
# Search by drug name
results = search_entities("aspirin", entity_types=["drug"])
# Returns: [{"id": "CHEMBL25", "name": "ASPIRIN", ...}]
Identifiers used:
- Targets: Ensembl gene IDs (e.g.,
ENSG00000157764) - Diseases: EFO (Experimental Factor Ontology) IDs (e.g.,
EFO_0000249) - Drugs: ChEMBL IDs (e.g.,
CHEMBL25)
2. Query Target Information
Retrieve comprehensive target annotations to assess druggability and biology.
from scripts.query_opentargets import get_target_info
target_info = get_target_info("ENSG00000157764", include_diseases=True)
# Access key fields:
# - approvedSymbol: HGNC gene symbol
# - approvedName: Full gene name
# - tractability: Druggability assessments across modalities
# - safetyLiabilities: Known safety concerns
# - geneticConstraint: Constraint scores from gnomAD
# - associatedDiseases: Top disease associations with scores
Key annotations to review:
- Tractability: Small molecule, antibody, PROTAC druggability predictions
- Safety: Known toxicity concerns from multiple databases
- Genetic constraint: pLI and LOEUF scores indicating essentiality
- Disease associations: Diseases linked to the target with evidence scores
Refer to references/target_annotations.md for detailed information about all target features.
3. Query Disease Information
Get disease details and associated targets/drugs.
from scripts.query_opentargets import get_disease_info
disease_info = get_disease_info("EFO_0000249", include_targets=True)
# Access fields:
# - name: Disease name
# - description: Disease description
# - therapeuticAreas: High-level disease categories
# - associatedTargets: Top targets with association scores
4. Retrieve Target-Disease Evidence
Get detailed evidence supporting a target-disease association.
from scripts.query_opentargets import get_target_disease_evidence
# Get all evidence
evidence = get_target_disease_evidence(
ensembl_id="ENSG00000157764",
efo_id="EFO_0000249"
)
# Filter by evidence type
genetic_evidence = get_target_disease_evidence(
ensembl_id="ENSG00000157764",
efo_id="EFO_0000249",
data_types=["genetic_association"]
)
# Each evidence record contains:
# - datasourceId: Specific data source (e.g., "gwas_catalog", "chembl")
# - datatypeId: Evidence category (e.g., "genetic_association", "known_drug")
# - score: Evidence strength (0-1)
# - studyId: Original study identifier
# - literature: Associated publications
Major evidence types:
- genetic_association: GWAS, rare variants, ClinVar, gene burden
- somatic_mutation: Cancer Gene Census, IntOGen, cancer biomarkers
- known_drug: Clinical precedence from approved/clinical drugs
- affected_pathway: CRISPR screens, pathway analyses, gene signatures
- rna_expression: Differential expression from Expression Atlas
- animal_model: Mouse phenotypes from IMPC
- literature: Text-mining from Europe PMC
Refer to references/evidence_types.md for detailed descriptions of all evidence types and interpretation guidelines.
5. Find Known Drugs
Identify drugs used for a disease and their targets.
from scripts.query_opentargets import get_known_drugs_for_disease
drugs = get_known_drugs_for_disease("EFO_0000249")
# drugs contains:
# - uniqueDrugs: Total number of unique drugs
# - uniqueTargets: Total number of unique targets
# - rows: List of drug-target-indication records with:
# - drug: {name, drugType, maximumClinicalTrialPhase}
# - targets: Genes targeted by the drug
# - phase: Clinical trial phase for this indication
# - status: Trial status (active, completed, etc.)
# - mechanismOfAction: How drug works
Clinical phases:
- Phase 4: Approved drug
- Phase 3: Late-stage clinical trials
- Phase 2: Mid-stage trials
- Phase 1: Early safety trials
6. Get Drug Information
Retrieve detailed drug information including mechanisms and indications.
from scripts.query_opentargets import get_drug_info
drug_info = get_drug_info("CHEMBL25")
# Access:
# - name, synonyms: Drug identifiers
# - drugType: Small molecule, antibody, etc.
# - maximumClinicalTrialPhase: Development stage
# - mechanismsOfAction: Target and action type
# - indications: Diseases with trial phases
# - withdrawnNotice: If withdrawn, reasons and countries
7. Get All Associations for a Target
Find all diseases associated with a target, optionally filtering by score.
from scripts.query_opentargets import get_target_associations
# Get associations with score >= 0.5
associations = get_target_associations(
ensembl_id="ENSG00000157764",
min_score=0.5
)
# Each association contains:
# - disease: {id, name}
# - score: Overall association score (0-1)
# - datatypeScores: Breakdown by evidence type
Association scores:
- Range: 0-1 (higher = stronger evidence)
- Aggregate evidence across all data types using harmonic sum
- NOT confidence scores but relative ranking metrics
- Under-studied diseases may have lower scores despite good evidence
GraphQL API Details
For custom queries beyond the provided helper functions, use the GraphQL API directly or modifyscripts/query_opentargets.py.
Key information:
- Endpoint:
https://api.platform.opentargets.org/api/v4/graphql - Interactive browser:
https://api.platform.opentargets.org/api/v4/graphql/browser - No authentication required
- Request only needed fields to minimize response size
- Use pagination for large result sets:
page: {size: N, index: M}
Refer to references/api_reference.md for:
- Complete endpoint documentation
- Example queries for all entity types
- Error handling patterns
- Best practices for API usage
Best Practices
Target Prioritization Strategy
When prioritizing drug targets:
- Start with genetic evidence: Human genetics (GWAS, rare variants) provides strongest disease relevance
- Check tractability: Prefer targets with clinical or discovery precedence
- Assess safety: Review safety liabilities, expression patterns, and genetic constraint
- Evaluate clinical precedence: Known drugs indicate druggability and therapeutic window
- Consider multiple evidence types: Convergent evidence from different sources increases confidence
- Validate mechanistically: Pathway evidence and biological plausibility
- Review literature manually: For critical decisions, examine primary publications
Evidence Interpretation
Strong evidence indicators:- Multiple independent evidence sources
- High genetic association scores (especially GWAS with L2G > 0.5)
- Clinical precedence from approved drugs
- ClinVar pathogenic variants with disease match
- Mouse models with relevant phenotypes
- Single evidence source only
- Text-mining as sole evidence (requires manual validation)
- Conflicting evidence across sources
- High essentiality + ubiquitous expression (poor therapeutic window)
- Multiple safety liabilities
- Scores rank relative strength, not absolute confidence
- Under-studied diseases have lower scores despite potentially valid targets
- Weight expert-curated sources higher than computational predictions
- Check evidence breakdown, not just overall score
Common Workflows
Workflow 1: Target Discovery for a Disease- Search for disease → get EFO ID
- Query disease info with
include_targets=True - Review top targets sorted by association score
- For promising targets, get detailed target info
- Examine evidence types supporting each association
- Assess tractability and safety for prioritized targets
- Search for target → get Ensembl ID
- Get comprehensive target info
- Check tractability (especially clinical precedence)
- Review safety liabilities and genetic constraint
- Examine disease associations to understand biology
- Look for chemical probes or tool compounds
- Check known drugs targeting gene for mechanism insights
- Search for disease → get EFO ID
- Get known drugs for disease
- For each drug, get detailed drug info
- Examine mechanisms of action and targets
- Look for related disease indications
- Assess clinical trial phases and status
- Identify repurposing opportunities based on mechanism
- Search for target of interest
- Get associated diseases with evidence
- For each disease, get known drugs
- Review clinical phases and development status
- Identify competitors and their mechanisms
- Assess clinical precedence and market landscape
Resources
Scripts
scripts/query_opentargets.pyHelper functions for common API operations:
search_entities()- Search for targets, diseases, or drugsget_target_info()- Retrieve target annotationsget_disease_info()- Retrieve disease informationget_target_disease_evidence()- Get supporting evidenceget_known_drugs_for_disease()- Find drugs for a diseaseget_drug_info()- Retrieve drug detailsget_target_associations()- Get all associations for a targetexecute_query()- Execute custom GraphQL queries
References
references/api_reference.mdComplete GraphQL API documentation including:
- Endpoint details and authentication
- Available query types (target, disease, drug, search)
- Example queries for all common operations
- Error handling and best practices
- Data licensing and citation requirements
Comprehensive guide to evid
Preview truncated. View the full source on GitHub →
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