Computational identification of synonymous SNPs in the human genome and their potential role in disease
The potential phenotypic effects of synonymous SNPs (sSNPs) have long been overlooked. Although several sSNPs are no longer thought to be silent, no one has identified which sSNPs may contribute to phenotypic variation on a genome-wide scale. sSNPs that cause a change in codon-usage frequency or...
Main Author: | Wood, Lee-Ann |
---|---|
Format: | Others |
Language: | en |
Published: |
2013
|
Subjects: | |
Online Access: | http://hdl.handle.net/10539/12309 |
Similar Items
-
Using SNPs to find my roots
by: Brenda Wingfield
Published: (2014-02-01) -
Sukkula retrotransposon movements in the human genome
by: Buket Cakmak, et al.
Published: (2017-07-01) -
Role of single nucleotide polymorphisms (SNPs) in common migraine
by: Sukhvinder Kaur, et al.
Published: (2019-07-01) -
Deep whole-genome resequencing sheds light on the distribution and effect of amphioxus SNPs
by: Chen, J.-Y, et al.
Published: (2022) -
What animals can teach us about evolution, the human genome, and human disease
by: Kerstin Lindblad-Toh
Published: (2020-02-01)