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  1. pdfSpring03.pdf 
    https://www.ncbi.nlm.nih.gov/books/NBK2592/bin/Spring03.pdf
    ... gene, APOLIV, one of its transcripts, and the coding sequence derived from the transcript, respectively. The transcript variant shown lacks exon 3. The Sequin graphical display ...
  2. pdfNational Library of Medicine - Programs and Services, Fiscal Year FY2009 
    https://www.nlm.nih.gov/ocpl/anreports/fy2009.pdf
    ... important variants in a timely fashion. Descriptions of variants were extracted from OMIM, GeneReviews, and Gene Tests, and processed for submission by dbSNP. The Consensus Coding Sequence (CCDS) database identifies a core set of consistently ...
  3. pdfNational Library of Medicine Programs and Services FY2010 
    https://www.nlm.nih.gov/ocpl/anreports/fy2010.pdf
    ... to dbSNP. The ongoing project will have all variants represented by OMIM assigned identifiers in dbSNP and dbVar by the end of FY2010. The Consensus CoDing Sequence (CCDS) database identifies a core set of consistently ...
  4. Gene filtering in NCBI Sequence Viewer - NCBI Insights 
    https://ncbiinsights.ncbi.nlm.nih.gov/.../08/20/gene-filtering-in-sv
    ... genome browser and other instances of the NCBI Sequence Viewer! Now, you ... protein-coding transcript variants are shown in your view. You can also ...
  5. pdfNational Library of Medicine Programs and Services FY2013 
    https://www.nlm.nih.gov/ocpl/anreports/fy2013.pdf
    ... year, the number of organisms supported by the sequence curation group increased by 119 percent to 94 distinct organisms. Curation of individual genes and alternate splice variants resulted in over 31,328 new or updated RefSeq protein-coding, non-coding, and pseudogene records for the 94 ...
  6. CNVs from Exome Aggregation Consortium (ExAC) added to dbVar in September 2017 data release - NCBI Insights 
    https://ncbiinsights.ncbi.nlm.nih.gov/...september-2017-data-release
    Skip to content Copy number variants (CNVs) from ... FTP files in VCF, GVF, and CSV formats, and include placements on GRCh37 as well ...
  7. pdfNational Library of Medicine Programs and Services FY2014 
    https://www.nlm.nih.gov/ocpl/anreports/fy2014.pdf
    ... and automated analysis of individual genes, alternate splice variants, and individual nucleotide mismatches (relative to the reference human genome sequence) resulted in over 47,634 new or updated RefSeq protein-coding, non-coding, and pseudogene records. During FY2014, 31, ...
  8. 5 NCBI articles in 2018 Nucleic Acids Research database issue - NCBI Insights 
    https://ncbiinsights.ncbi.nlm.nih.gov/...ids-research-database-issue
    ... sequences, and an Identical Protein Groups resource. “Consensus coding sequence (CCDS) database: a standardized set of human and ... M Nudge et al. (PMID: 29126148 ) The Consensus Coding Sequence (CCDS) project provides a dataset of protein-coding ...
  9. Meet the Experts 
    https://www.nlm.nih.gov/ncbi/conferences/ASHG/ASHG_experts.html
    ... for Identification and Analysis of Common and Somatic Variants ... reference sequence standards of coding and non-coding loci for all vertebrates. Before ...
  10. CCDS Release 24 - NCBI Insights 
    https://ncbiinsights.ncbi.nlm.nih.gov/2022/11/02/ccds-release-24
    ... of human protein-coding regions from the Consensus Coding Sequence (CCDS) collaboration Are you interested in a set ... provide a set of reference transcripts for clinical variant reporting and other research applications. The main difference ( ...
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