You’re offline. This is a read only version of the page.
Toggle navigation
National Library of Medicine
National Library of Medicine
Support Center Home
NLM Support Center
Knowledge Base
Submit Data
Submit Data
Search the Knowledge Base
How do I use Nucleotide BLAST (blastn) and CDS feature display to determine if a protein-coding sequence has poor quality or incorrect nucleotide substitutions?
How do I associate my virus sequences in GenBank with my data in the Sequence Read Archive (SRA)?
I have sequenced an entire genome (transcriptome). How do I submit it to GenBank?
Will I be able to keep my submitted sequence/molecular data confidential at NCBI until I publish my paper?
Why am I getting an error message stating that the GenBank submission system (BankIt) is unavailable?
How do I change the release date of my GenBank and Sequence Read Archive (SRA) records?
What are GenBank accession numbers and what information is embedded in them?
How do I interpret Nucleotide BLAST (blastn) pairwise alignments with the CDS feature display?
How do I use Nucleotide BLAST (blastn) to determine the coding locations on a sequence from a prokaryotic genome?
How are GenBank accession numbers assigned to my submission?
Why do I get error messages when I try to annotate a coding region (CDS) in BankIt?
How do I find the release date and/or any update date of a GenBank (Nucleotide) sequence record?
What kind of sequences can I submit to GenBank using BankIt?
Where and how do I submit individual human variation data associated with phenotypes at NCBI?
How do I set up Nucleotide BLAST (blastn) to analyze coding regions (CDS) on sequences that I am submitting to GenBank?
How do I use Nucleotide BLAST (blastn) and the CDS feature display to determine the coding locations for eukaryotic genes (those with intron/exon structure)?
How do I use Nucleotide BLAST (blastn) with CDS feature display to determine the coding strand (plus or minus) on my sequences?
How do I use Nucleotide BLAST (blastn) with CDS feature display to determine the reading frame of a 5’ partial CDS?
How do I use Nucleotide BLAST (blastn) with CDS feature display to determine if there are sequence quality problems at the ends of my sequences?
How do I use Nucleotide BLAST (blastn) and CDS feature display to determine if I have nucleotide insertions or deletions in my sequence that may cause reading frame shifts?
