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Circulation: Cardiovascular Genetics
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Circulation: Cardiovascular Genetics. 2009;2:530-536
doi: 10.1161/CIRCGENETICS.109.872010
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Methods in Genetics and Clinical Interpretation

Single-Nucleotide Polymorphism Bioinformatics

A Comprehensive Review of Resources

Andrew D. Johnson, PhD

From the National Heart, Lung, Blood Institute’s Framingham Heart Study, Framingham, Mass.

Correspondence to Andrew D. Johnson, PhD, NHLBI Framingham Heart Study, 73 Mt Wayte Ave, Suite 2, Framingham, MA 01702. E-mail johnsonad2@nhlbi.nih.gov


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 


    Introduction
 
Recent years have seen near exponential growth in knowledge regarding genetic and genomic variation as more genomes have been sequenced, and corresponding advances and economies of scale in sequencing and genotyping technologies have reduced their relative costs. In parallel with these developments, discoveries of genes contributing to monogenic and complex diseases have rapidly advanced, and bioinformatics databases and software relating to the collection and analysis of genetic data have increased in number, size, and scope. Single-nucleotide polymorphisms (SNPs), comprising the most abundant type of genetic variation, are now the principal raw material underlying most genetic studies and databases. Although other types of variation, including indels, microsatellites, copy number variants, and epigenetic markers remain important to consider and can impact disease, SNPs are largely the easiest to ascertain and the most useful and widely applied markers in genetic studies in the modern age.

Researchers and clinician-researchers are confronted with a dizzying array of software choices and increasingly large and complex datasets and databases relating to SNPs, sometimes working without assistance from a geneticist or a bioinformatician to help guide them. The principle aim of this review is to provide a comprehensive overview of available bioinformatics resources relating to human genetics research, with an emphasis on SNP-centered resources. The review also provides a resource for students seeking an introduction to SNP genetics resources and for wet laboratory molecular biologists conducting SNP-centered research who want to expand their knowledge on ways to apply SNP tools and databases. A number of important issues that . . . [Full Text of this Article]