How are the immunoglobulin and T-cell receptor loci annotated for the human and mouse genomes? How are PubMed IDs selected for inclusion in RefSeq? What feature annotation is included on RefSeq records? Why is the gene symbol or protein name in a RefSeq record different from the symbol or name used in related INSDC records? How can I tell if a RefSeq record has been curated? Where can I find a report of suppressed or replaced accessions? Where can I download the human proteome or transcriptome? Why are there gaps in sequentially numbered files in the RefSeq release? What data are available for FTP download? NCBI’s annotation displayed on a genomic RefSeq record may include ‘unclassified transcription discrepancy’ and ‘unclassified translation discrepancy’ exceptions on the mRNA and CDS features, respectively. What is a readthrough locus and how is it represented? Why is a transcript RefSeq record made from genomic sequence instead of available transcripts? Why are some splice variants for my favorite gene missing in the RefSeq set? Why aren't RefSeq records made for all organisms or for all of the loci available in Gene? How can I evaluate the support for a RefSeq transcript or protein? How do I cite the RefSeq project, a species-specific dataset, or individual RefSeq records? If RefSeq is a non-redundant database why does my BLAST query return hits to more than one RefSeq accession? How can I quickly identify RefSeq records? The sequence of a RefSeq accession is identical to that of a GenBank accession. What is the difference between RefSeq and GenBank? What sequence is used to define a RefSeq? What is an NG_ accession and why are they made? What is the difference between XM_ and NM_ accessions? Where can I find more information about the NCBI RefSeq project? What are the distinguishing features of a RefSeq record?
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