SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
- PMID: 18974171
- PMCID: PMC2720775
- DOI: 10.1093/bioinformatics/btn564
SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap
Abstract
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/.
Figures
References
-
- Barrett JC, et al. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005;21:263–265. - PubMed
-
- Helgadottir A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007;316:1491–1493. - PubMed
-
- Liefeld T, et al. GeneCruiser: a web service for the annotation of microarray data. Bioinformatics. 2005;21:3681–3682. - PubMed
-
- Marchini J, et al. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat. Genet. 2007;39:906–913. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
