Single-nucleotide Polymorphisms
Single-nucleotide polymorphisms (SNPs, pronounced “snips”) are the most common type of genetic variation among people. Each Single-nucleotide polymorphisms represents a difference in a single nucleotide. For example, a single-nucleotide polymorphisms may replace the cytosine (C) with the thymine (T) in a certain strech of DNA. SNPs occur normally throughout a person’s DNA and these variations are usually harmless and do not affect health or development. However, some SNPs are associated with health conditions or disease predisposition, and others may influence how an individual responds to certain drugs. SNPs are also valuable in biomedical research and genetic testing because they can act as biological markers, helping scientists locate disease-associated genes.
Single-nucleotide Polymorphisms
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VarSAn – Computational tool to identify disease pathways
Researchers at the University of Illinois Urbana-Champaign have developed a new computational tool to identify pathways related to diseases, including breast and prostate cancer, using single-nucleotide polymorphisms (SNPs). The tool, called VarSAn (Variant Set Annotator, pronounced ‘version’),…

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