ClinVar Genetic Variants Scraper — Variant Pathogenicity Data

NCBI ClinVar Variant Scraper

parseforge/clinvar-esummary-scraper

Query NCBI ClinVar for human genetic variants tied to disease. Search by gene symbol, variant ID, or clinical significance and pull variation IDs, gene info, molecular consequence, clinical assertions, and review status. Useful for clinical genomics, variant curation, and research.

NCBI ClinVar Variants Scraper - Genetic Variation Data

parseforge/ncbi-clinvar-variants-scraper

Sweep medical and biomedical records from Ncbi Clinvar Variants with names, identifiers, classifications, descriptions, status and source links. Ideal for healthcare research, pharma teams and clinical analytics. Run on demand or on a recurring schedule and feed every row into your favourite anal.

NCBI dbSNP Variant Scraper

parseforge/dbsnp-esummary-scraper

Search NCBI dbSNP for short genetic variants by gene symbol or rs ID. Returns rs accession, chromosome position, allele info, gene context, and global minor allele frequencies. Useful for GWAS pipelines, variant annotation, population genetics, and pharmacogenomics work.

Clinical Trial Multi-Source Aggregator

parseforge/clinical-trial-multi-source-scraper

Search active and historical clinical trials across the EU CTIS, WHO, openFDA and ClinVar variants in one query. Pull trial IDs, sponsors, phases, conditions, locations, status and outcome data. Built for pharma research, patient navigators and biotech analysts.

NCBI EUtils Gene Summary Scraper

parseforge/ncbi-eutils-gene-summary-scraper

Pull gene summaries from NCBI EUtils by Gene UID, returning official symbol, full name, aliases, organism, chromosome, map location, and description. Useful for annotating variant lists, building gene knowledge panels, and enriching bioinformatics dashboards with canonical NCBI metadata.

NCBI Gene Database Scraper

parseforge/ncbi-eutils-gene-scraper

Query NCBI Gene through Entrez syntax such as BRCA1[gene] AND human[orgn]. Returns gene symbol, description, organism, chromosome, map location, summary, aliases, and designations. Useful for genomics pipelines, target discovery, and clinical research across model organisms.

NCBI dbSNP Variants Scraper

parseforge/ncbi-dbsnp-variants-scraper

Discover medical and biomedical records from Ncbi Dbsnp Variants with names, identifiers, classifications, descriptions, status and source links. Ideal for healthcare research, pharma teams and clinical analytics. Run on demand or on a recurring schedule and feed every row into your favourite ana.

NCBI Gene Lookup — Genomics API for Pharma R&D

azureblue/ncbi-gene-scraper

Search NCBI Gene via E-utilities. Returns gene symbol, full name, chromosome location, map locus, aliases, OMIM ID, organism and functional summary.

IntAct Molecular Interactions Scraper

parseforge/intact-interactions-scraper

Search the EMBL EBI IntAct database for curated molecular interaction evidence. Query by gene or protein name and retrieve interactor pairs, interaction types, detection methods, source publication IDs, and confidence scores. Useful for systems biology and interactome research.

Shopify Store Products Scraper - Products, Variants & Prices

fascinating_lentil/shopify-store-products-scraper

Scrape products, variants, prices, images, vendors, and tags from any Shopify store. No login or API key needed. Export to JSON, CSV, or Excel.