| name | ncbi-integrated-research |
| description | Run bounded NCBI-centered research across Gene, PubMed/PMC, sequence, variation, and GEO-linked records. Use when a gene, accession, sequence, or literature question requires traceable NCBI cross-links. |
| license | MIT |
NCBI Integrated Research
- Resolve the canonical human gene with
science_search_ncbi_gene; preserve species and Entrez ID.
- Select only required lanes: PubMed literature, PMC open text, sequence/Datasets, ClinVar/dbSNP variation, or GEO metadata.
- Follow explicit database links rather than repeating broad free-text searches. Bound each result set and respect NCBI rate policy.
- Preserve database, endpoint, query, IDs, link relation, release/access time, and raw artifact path when saved.
- Render PMIDs and DOIs as links; distinguish metadata, abstract, full text, sequence record, and curated assertion.
- Reconcile evidence with primary publications and
$science-review before conclusions.
Do not treat NCBI summaries as clinical guidance. Do not download large sequence or GEO payloads without a declared file and compute plan.
Store cross-database link paths and identifiers with $science-provenance before review.