Submit data to NCBI
Genetic sequence database, an annotated collection of all publicly available DNA sequences. Submit Bacterial or Archaeal 16S ribosomal RNA sequences via the 16S rRNA Submission Tool (beta version) wizard. All other submission types should use one of the alternate submission tools (e.g. BankIt, Sequin, tbl2asn, etc.)
The Whole Genome Shotgun (WGS) database accepts prokaryotic and eukaryotic genomes that are draft or incomplete. This submission portal was updated on Feb. 3, 2014, and now accepts fasta sequences. To access submissions started before that date, go to the previous version of the portal.
Collection of genomic sequences that are used to represent the genome of an organism.
Computationally assembled sequences from primary data such as ESTs, traces and Next Generation Sequencing Technologies. TSA sequence records differ from EST and GenBank records because there are no physical counterparts to the assemblies.
The Sequence Read Archive (SRA) stores raw and aligned sequence data from NextGen sequencing platforms.
The new submission interface for SRA. Data files can only be uploaded through this interface using the Aspera Connect plugin. Please use the other SRA submission tool if you need to upload your data using FTP or Aspera command line.
Next generation sequence submissions for functional genomic studies that examine gene expression, regulation or epigenomics.
A collection of biological data related to a single initiative, originating from a single organization or from a consortium.
Descriptions of biological source materials used in experimental assays.
Genetic tests for inherited and somatic genetic variations, including newer types of tests such as arrays and multiplex panels.
Variation resources at NCBI: dbSNP, dbVar and ClinVar. dbSNP represents short variation in any organism including single nucleotide variants, insertions, deletions, and microsatellites. dbVar represents genomic structural variations from studies submitted on any organism or phenotype. ClinVar aggregates information about human sequence variation and its relationship to human health.