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SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap.

http://www.ncbi.nlm.nih.gov/pubmed/18974171

SUMMARY: The interpretation of genome-wide association results is confounded by linkage disequilibrium between nearby alleles. We have developed a flexible bioinformatics query tool for single-nucleotide polymorphisms (SNPs) to identify and to annotate nearby SNPs in linkage disequilibrium (proxies) based on HapMap. By offering functionality to generate graphical plots for these data, the SNAP server will facilitate interpretation and comparison of genome-wide association study results, and the design of fine-mapping experiments (by delineating genomic regions harboring associated variants and their proxies). AVAILABILITY: SNAP server is available at http://www.broad.mit.edu/mpg/snap/.

Pubmed ID: 18974171 RIS Download

Mesh terms: Genome, Human | Genome-Wide Association Study | Genotype | Humans | Internet | Linkage Disequilibrium | Polymorphism, Single Nucleotide | Software

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Associated grants

  • Agency: NHLBI NIH HHS, Id: N01-HC-25195
  • Agency: NHLBI NIH HHS, Id: N01-HC-65226
  • Agency: Intramural NIH HHS, Id:

Mouse Genome Informatics (Data, Gene Annotation)

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