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What is SNP

Handbook of Research on Computational and Systems Biology: Interdisciplinary Applications
A form of genetic variation represented as a single nucleotide polymorphism.
Published in Chapter:
Addressing the Challenges of Detecting Epistasis in Genome-Wide Association Studies of Common Human Diseases Using Biological Expert Knowledge
Kristine A. Pattin (Dartmouth Medical School, USA) and Jason H. Moore (Dartmouth Medical School, USA)
DOI: 10.4018/978-1-60960-491-2.ch006
Abstract
Recent technological developments in the field of genetics have given rise to an abundance of research tools, such as genome-wide genotyping, that allow researchers to conduct genome-wide association studies (GWAS) for detecting genetic variants that confer increased or decreased susceptibility to disease. However, discovering epistatic, or gene-gene, interactions in high dimensional datasets is a problem due to the computational complexity that results from the analysis of all possible combinations of single-nucleotide polymorphisms (SNPs). A recently explored approach to this problem employs biological expert knowledge, such as pathway or protein-protein interaction information, to guide an analysis by the selection or weighting of SNPs based on this knowledge. Narrowing the evaluation to gene combinations that have been shown to interact experimentally provides a biologically concise reason why those two genes may be detected together statistically. This chapter discusses the challenges of discovering epistatic interactions in GWAS and how biological expert knowledge can be used to facilitate genome-wide genetic studies.
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More Results
Analysis of Large-Scale OMIC Data Using Self Organizing Maps
Single nucleotide polymorphisms are persistent mutations of a single base pair in the genome. They are the most frequent source of DNA sequence variation among humans.
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Alternative Isoform Detection Using Exon Arrays
Single nucleotide polymorphism. SNPs are single base pair mutations which have been driven to detectable frequencies in human populations. On average, two human individuals will differ at 1 polymorphic site for each 1000 bp of DNA. Vast majority of the SNPs are likely to be neutral, but some may affect phenotypic traits.
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Genetic Processes Facilitating Pathogen Emergence
Single nucleotide polymorphism, that is a change in a single nucleotide in a DNA sequence.
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