Submission Portal

Suggested tools

• SRA

  SRA accepts unassembled reads from high throughput sequencing platforms. Submitted data files should generally be minimally processed and include per-base quality scores.

• SRA

  Submit unassembled reads of SARS-CoV-2 with BioProject, BioSample, metadata and NGS files.

• GEO

  GEO accepts raw data, processed data and metadata for gene expression and epigenomics datasets generated by high-throughput sequencing and microarray technologies.

• Genome

  Submit assembled complete or incomplete/draft prokaryotic and eukaryotic genomes. Not for viral, phage, or single locus sequences (for example: 16S rRNA). Submit those to regular GenBank.

• TSA

  Computationally assembled transcribed RNA sequences representing a transcriptome derived from sequence reads submitted to Sequence Read Archive (SRA).

• GenBank

  Submit ribosomal RNA (rRNA), rRNA-ITS, SARS-CoV-2, Influenza, Norovirus, Dengue, metazoan COX1 or eukaryotic nuclear mRNA

• GenBank

  Submit assembled reads of SARS-CoV-2 with FASTA files and source metadata. Annotation for SARS-CoV-2 is not required.

• GenBank

  Eukaryotic nuclear mRNAs (limit 499 sequences)

• BankIt

  other mRNAs

• BankIt

  Submit genomic DNA, organelle, ncRNA, plasmids, other viruses, phages, mRNA and synthetic constructs.

• dbGaP

  Microarray data from clinical studies that require controlled access.

• ClinVar

  Information on human sequence variation and relationship to human health.

• NIHMS

  Submit the electronic version of a peer-reviewed manuscript for inclusion in PubMed Central.

• ClinicalTrials.gov

  Explore clinicial studies conducted around the world.

• TLS

  Large-scale sequencing projects for an individual loci are taken in GenBank & Sequence Read Archive (SRA).

• Supplementary Files

  Submit BioNano maps, Beta-lactamase gene, and PacBio methylation data.

• Third Party Annotation (TPA)

  NCBI takes data capturing experimental or inferential results supporting annotation dervied from GenBank primary data.

• dbSNP

  Small human genomic variation: single nucleotide, insertions, deletions, and microsatellites.

• GTR

  Genetic tests for inherited & somatic genetic variations, including arrays and multiplex panels.

• BioProject and BioSample

  Automatically create a BioProject and BioSample during sequence data submission.

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We need a little more information. Add to your description above, indicating sequence data type and/or whether your data is assembled, unassembled or expression data.