oanor
Iscriviti gratis
Mercata Prezzi Caratteristiche Accedi

API · /dbvar-api

Structural Variants API

salutare 3,231 Abbonati

Human genomic structural variation as an API — powered by NCBI dbVar, the archive of structural variants (SVs): copy-number variants (CNVs), large deletions, duplications, insertions, inversions and translocations, typically larger than 50 base pairs. This is the structural counterpart to single-nucleotide variant databases: search structural variants overlapping a gene (or by free text) and get each variant's dbVar accession, the study it came from, its type, the genes it overlaps, its genomic placement on GRCh38 and its clinical significance; then look up any variant for the full record — placements on both GRCh37 and GRCh38 assemblies, variant type, genes, clinical significance, study type, methods and variant counts. From BRCA1 CNVs to Cri-du-chat deletions, it is ideal for genomics, cytogenetics, rare-disease and bioinformatics work. A structural-variation / CNV resource — distinct from clinical single-nucleotide variant interpretation (ClinVar), population allele frequencies (gnomAD) and trait associations (GWAS). Open data from NCBI dbVar (public domain).

#structural-variants #cnv #genomics #variants #bioinformatics #dbvar
api.oanor.com/dbvar-api
Ottieni una chiave API Prova nel parco giochi → Contatta provider

Specifica leggibile dalle macchine, così gli agenti AI possono integrare questa API.

/api/dbvar-api/openapi.json
/api/dbvar-api/llms.txt

Individuazione: GET /api/index.json elenca ogni API.

API salute

salutare
Tempo di attività
100.00%
Sondaggi del server · 24 ore su 24
Latenza media
653 ms
Sondaggi del server · 24 ore su 24
Abbonati
3,231
attiva
Chiamate totali
0
ultimi 7 giorni
status Pagina di stato completa → · 3 sonde/24h

Prezzi

Scegli un livello: fatturazione mensile, annullamento in qualsiasi momento.

Free

Gratis

  • 2,280 chiamate/mese
  • 2 richieste/secondo
  • Tetto rigido (429 sopra la quota, nessuna eccedenza)
  • 2,280 llamadas/mes
  • 2 solicitudes/seg
  • Búsqueda + consulta de variantes
  • Sin tarjeta de crédito
Accedi per abbonarti

Starter

€6.45 /mese

  • 45,500 chiamate/mese
  • 8 richieste/secondo
  • Tetto rigido (429 sopra la quota, nessuna eccedenza)
  • 45.5k calls/month
  • 8 req/sec
  • GRCh37 + GRCh38 placements
  • Email support
Accedi per abbonarti

Pro

€21.00 /mese

  • 228,000 chiamate/mese
  • 20 richieste/secondo
  • Tetto rigido (429 sopra la quota, nessuna eccedenza)
  • 228k calls/month
  • 20 req/sec
  • Genomics & cytogenetics apps
  • Priority support
Accedi per abbonarti

Mega

€56.90 /mese

  • 830,000 chiamate/mese
  • 50 richieste/secondo
  • Tetto rigido (429 sopra la quota, nessuna eccedenza)
  • 830k calls/month
  • 50 req/sec
  • Variant-analysis platform
  • Dedicated SLA
Accedi per abbonarti

Costruito da

P
PremiumApi

Correlato APIs

Altro APIs con tag sovrapposti.

Genome Assemblies API

Reference genome assemblies as an API — powered by NCBI Assembly, the registry of genome builds for organisms across the tree of life. Search assemblies by organism (or free text) and look up any assembly's metadata: its accession (GCF_… RefSeq or GCA_… GenBank), name (e.g. GRCh38.p14), organism and taxon id, assembly level (complete genome, chromosome, scaffold or contig), contiguity statistics (contig and scaffold N50), sequencing coverage, RefSeq category, UCSC and Ensembl names, the submitting organization, release date and FTP download paths. From the human reference genome to any sequenced microbe, plant or animal, it turns the genome-assembly registry into a clean search-and-fetch API. A genome-assembly registry — distinct from sequence (ENA), genome annotation (Ensembl), variant (ClinVar, dbVar) and gene-expression (GEO) databases. Open data from NCBI Assembly (public domain).

api.oanor.com/genomes-api

Gene Expression API

Functional-genomics experiments as an API — powered by NCBI GEO (Gene Expression Omnibus), the largest public repository of gene-expression data. GEO archives expression series and curated datasets from microarray and high-throughput-sequencing experiments across every organism. Search experiments by keyword and optionally by organism, and look up any series or dataset to get its metadata: title, summary, assay type (expression profiling by array or by sequencing), organism, number of samples, platform and the publication behind it. From β-cell stress studies to cancer transcriptomics across human and mouse, it turns the GEO archive into a simple search-and-fetch API for transcriptomics, bioinformatics and research-data discovery. A gene-expression / functional-genomics dataset repository — distinct from sequence (ENA), variant (ClinVar, dbVar), structure (PDB) and ontology databases. Open data from NCBI GEO (public domain).

api.oanor.com/geodatasets-api

Protein Interactions API

Protein-protein interaction networks as an API — powered by STRING, the database of known and predicted protein associations that combines evidence from laboratory experiments, curated pathway databases, gene co-expression, genomic context and automated text mining into a single confidence score, across thousands of organisms. Get a protein's top interaction partners (each with the combined confidence score and the seven evidence-channel subscores), the interaction network among any set of proteins as scored edges, and functional enrichment for a gene set — the over-represented GO terms, KEGG pathways, Pfam domains and more, each with its p-value, FDR and member genes. Pass gene symbols (TP53) or STRING/Ensembl ids, for human (default) or any species by NCBI taxon id. It is a cornerstone of systems biology — ideal for network analysis, functional genomics, pathway and bioinformatics tools. A protein-interaction-network resource — distinct from biological pathways (Reactome), curated protein complexes (Complex Portal) and Gene Ontology annotations (QuickGO). Open data from STRING (CC BY 4.0).

api.oanor.com/stringdb-api

Polygenic Scores API

Polygenic (risk) scores as an API — powered by the NHGRI-EBI PGS Catalog, the open database of published polygenic scores: weighted combinations of genetic variants used to estimate a person's genetic predisposition to a trait or disease. Search traits by name to find their ontology ids, list every polygenic score developed for a trait, and read a score's full metadata — the reported and mapped (EFO/MONDO) traits, the number of variants in the score, the development method, genome build, the ancestry distribution of the samples it was built and evaluated on, the publication behind it (title, journal, date, PubMed id), the release date, license and a direct link to the scoring file. From breast cancer and coronary artery disease to type 2 diabetes and BMI, it is ideal for statistical genetics, genomics, risk-prediction research and bioinformatics tools. A polygenic-score / genetic-risk-prediction resource — distinct from single-variant association studies (GWAS Catalog), population allele frequencies (gnomAD) and clinical variant interpretation (ClinVar). Open data from the NHGRI-EBI PGS Catalog (CC BY 4.0).

api.oanor.com/pgs-api

Domande frequenti

Risposte rapide su prezzi, quote e integrazione.

Come ottengo una chiave API per Structural Variants API?
Registrati gratuitamente su oanor.com, genera una chiave API dalla dashboard sviluppatore e chiama Structural Variants API con l'header x-oanor-key. Nessuna carta di credito richiesta per il piano gratuito.
Qual è il limite di velocità di Structural Variants API?
Il piano gratuito consente 1 richiesta al secondo. I piani a pagamento arrivano fino a 50 richieste al secondo nel piano Mega. I limiti rigorosi restituiscono HTTP 429 oltre la quota — nessuna spesa imprevista.
Quanto costa Structural Variants API?
Structural Variants API ha un piano gratuito con 100 chiamate / mese. I piani a pagamento partono da €6.45 / mese con quote più alte e limiti di velocità più rapidi.
Posso cancellare l'abbonamento in qualsiasi momento?
Sì. I piani sono fatturati mensilmente e puoi cancellare in qualsiasi momento dalla dashboard di fatturazione. Nessun contratto a lungo termine e nessuna penale di cancellazione.
Structural Variants API è conforme al GDPR?
Tutte le richieste a Structural Variants API passano attraverso il nostro gateway in UE. La tua chiave upstream non lascia mai il nostro server e nessun dato personale viene condiviso con il fornitore upstream oltre alla richiesta inviata.

Scegli un endpoint dall'elenco a sinistra per visualizzarne i dettagli e provarlo.

Frammenti di codice

Iscriviti per ottenere una chiave API, quindi chiama qualsiasi percorso sotto il tuo slug.

curl https://api.oanor.com/dbvar-api/SOME_PATH \
  -H "x-oanor-key: oanor_test_..."
const res = await fetch("https://api.oanor.com/dbvar-api/SOME_PATH", {
  headers: { "x-oanor-key": "oanor_test_..." }
});
const data = await res.json();
$ch = curl_init("https://api.oanor.com/dbvar-api/SOME_PATH");
curl_setopt($ch, CURLOPT_RETURNTRANSFER, true);
curl_setopt($ch, CURLOPT_HTTPHEADER, ["x-oanor-key: oanor_test_..."]);
$response = curl_exec($ch);
import requests
r = requests.get(
    "https://api.oanor.com/dbvar-api/SOME_PATH",
    headers={"x-oanor-key": "oanor_test_..."},
)
print(r.json())

Valutazioni

Accedi per votare.

Nessuna recensione ancora.

Discussione

Fai domande, condividi consigli, ricevi risposte dal provider e dagli altri sviluppatori. Pubblico — chiunque può leggere.

Accedi per scrivere o rispondere.

Accedi

Nuova discussione

/ 4000

📌 Fissato 🔒 Bloccato

·

· ·

/ 4000

🔒 Discussione bloccata — non si può più rispondere.

  • Nessuna discussione — inizia tu.

Supporto

Supporto privato 1:1 con il provider — fatturazione, integrazione, account. Solo tu e il team del provider vedete questi thread.

Accedi per aprire un ticket di supporto.

Accedi

Apri nuovo ticket

Descrivi cosa ti serve. Il team del provider riceve un'email e risponde sulla pagina del ticket.

  • Nessun ticket per questa API.

Abbonamento attivo: le chiamate possono iniziare subito.

Invia la tua prima richiesta —

Abbonamento attivo: copia uno snippet e avvia la tua prima chiamata.