- ... he performed whole-exome sequencing to identify functional non-synonymous variants in protein-coding regions associated with atrophy rate of hippocampal volume. ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... Examples include markers for sequence variation such as SNPs, or single nucleotide polymorphisms, and genomic position landmarks ... Reference Sequence (RefSeq) database provides a comprehensive, integrated, non-redundant set of sequences, including genomic DNA, transcript ( ...
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