Queries the NCBI Gene database to retrieve comprehensive genomic information, including sequences, annotations, and functional data.
The Gene Database skill integrates Claude with NCBI's E-utilities and Datasets APIs, enabling seamless retrieval of genomic data directly within your development or research workflow. It allows users to search for genes by symbol, name, or ID to fetch detailed reference sequences (RefSeqs), map chromosomal locations, and explore Gene Ontology (GO) annotations or phenotypes. Designed for bioinformatics and clinical research, this skill handles the complexities of NCBI's APIs, including rate limiting, batch processing for large datasets, and multi-format data parsing (JSON, XML, FASTA) to support gene annotation and functional analysis pipelines.
주요 기능
01Dual API support for NCBI E-utilities and the modern Datasets API
02Automated batch lookup for processing multiple gene identifiers efficiently
03Biological context searching by phenotype, disease, or chromosome location
04Standardized error handling and rate limit management for NCBI services
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06Comprehensive metadata retrieval including RefSeqs, GO terms, and pathways
사용 사례
01Automating gene annotation for bioinformatics data pipelines
02Cross-referencing gene symbols with official NCBI IDs and aliases
03Fetching reference sequences and mapping data for genomic analysis