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5 results
  1. NLM Grantee Spotlight 
    https://www.nlm.nih.gov/ep/Spotlight1.html
    ... he performed whole-exome sequencing to identify functional non-synonymous variants in protein-coding regions associated with atrophy rate of hippocampal volume. ...
  2. pdffy2002.pdf 
    https://www.nlm.nih.gov/ocpl/anreports/fy2002.pdf
    ... with NR_ was added to RefSeq and represents non-protein coding RNAs. The most common forms of sequence variations are single nucleotide polymorphisms, or SNPs. SNP detection and discovery is expected to facilitate ...
  3. pdfNational Library of Medicine Programs and Services FY2014 
    https://www.nlm.nih.gov/ocpl/anreports/fy2014.pdf
    ... over 47,634 new or updated RefSeq protein-coding, non-coding, and pseudogene records. During FY2014, 31,432 ... Los Angeles Gerek, Zeynep N Computational diagnosis of non-synonymous variations using structural dynamics 1 R21 LM011941-01 ...
  4. pdf2012 NLM Training Conference 
    https://www.nlm.nih.gov/.../TC2012TrainingConferenceBook.pdf
    ... 1q41, 3q22.3 and 15q21.3. Only one SNP lies within a known gene, NEDD4 on chromosome ... sample size from genome-wide single nucleotide polymorphism (SNP) data. Phenotypes were simulated for case-control datasets ...
  5. pdfNational Library of Medicine - Programs and Services, Fiscal Year 2003 
    https://www.nlm.nih.gov/ocpl/anreports/fy2003.pdf
    ... Examples include markers for sequence variation such as SNPs, or single nucleotide polymorphisms, and genomic position landmarks ... common human polymorphisms for the international research community. SNP detection and discovery is expected to facilitate large- ...