The National Center for Biotechnology Information (NCBI) is part of the National Library of Medicine at the National Institutes of Health. NCBI supports research in computational biology, develops software tools for sequencing analysis, and creates and maintains public bioinformatics databases.
It provides BLAST, a tool for determining sequence similarity. And among its many databases for exploring human and other genomes are Nucleotide for sequence, dbSNP for small-scale variation, and Gene for comprehensive, aggregated information relating to individual genes.
The phrase "genomics gateway" is used here to refer to an online collection of databases and tools related to genomes and genes.
Genomics gateways have a broad scope, typically encompassing databases on genes, variation, sequence, gene expression, genotype-phenotype relationships, etc. Examples of genomics gateways include those maintained by the NCBI, EMBL-EBI and SRI International (e.g., BioCyc).
Additional features of genomics gateways include:
Genomics gateways are excellent destinations for launching explorations of genes and genomes. They offer similar searching and analysis tools and work from a shared set of genomic data. Despite this similarity, each repository has unique functionalities for discovery, visualization, and analysis.
NCBI maintains a suite of DNA and RNA resources, including databases, downloadable software and sequence collections, resources to support the submission of sequence and other data, tools for searching and sequence analysis, and how-tos related to submitting sequence, finding sequence, designing PCR primers, etc.
The following are four core genomic sequence databases that are part of this broader collection of DNA and RNA resources.