NCBI (PubMed, Gene, ClinVar, dbSNP) integration
Search PubMed, Gene, ClinVar, dbSNP and other NCBI databases through the official E-utilities, get record summaries and full records, and get alerts for new PubMed articles. Read-only and free.
Build it by describing it
Type a sentence like this and the copilot builds, validates and simulates the workflow.- Simulated before it goes live
- Fixes proposed when something breaks
- One credit per run
Triggers
Start a workflow when this happens- WHENNew PubMed Article
Triggers when a new article matching your search is added to PubMed. Great for literature alerts on a gene, disease or technique.
Actions
Then Calibra can do this for you- DOSearch PubMed Articles
Searches PubMed with the same query syntax as the PubMed website and returns each article's title, authors, journal, date, DOI and link.
- DOGet PubMed Articles
Gets the title, authors, journal, date, DOI and link of one or more PubMed articles from their PMIDs.
- DOSearch NCBI Database
Searches any NCBI database (Gene, ClinVar, dbSNP, PubMed, Protein…) and returns the matching IDs and, optionally, the summary of each record.
- DOGet Record Summaries
Gets the summary of one or more records from an NCBI database (Gene, ClinVar, dbSNP, Protein…) from their IDs.
- DOFetch Full Records
Downloads the full content of NCBI records in a chosen format: PubMed abstracts, MEDLINE, Gene tables, ClinVar XML, FASTA sequences and more.
- DOCustom NCBI E-utilities Request (read-only)
Makes a GET request to any NCBI E-utilities endpoint (einfo, esearch, esummary, efetch, elink…). Your contact email, tool name and API key are added automatically.
Questions
Is the NCBI (PubMed, Gene, ClinVar, dbSNP) integration free?
Yes. NCBI (PubMed, Gene, ClinVar, dbSNP) is available on every Calibra plan, including the free plan, which needs no card.
How is NCBI (PubMed, Gene, ClinVar, dbSNP) usage billed?
Calibra charges one credit per workflow run, however many steps it has. Steps that read from or write to this app do not cost extra.
Can I connect NCBI (PubMed, Gene, ClinVar, dbSNP) without writing code?
Yes. Describe the process in plain words and the AI copilot builds the workflow with NCBI (PubMed, Gene, ClinVar, dbSNP) for you. You can also use templates or the visual editor.
Describe your first process. Watch it run today.
Free plan, no card. One credit per run, however many steps it has.