SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap - PubMed (original) (raw)

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

Andrew D Johnson et al. Bioinformatics. 2008.

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/.

PubMed Disclaimer

Figures

Fig. 1.

Fig. 1.

Regional LD plot for SNPs rs10757278 and rs10811661 at 9p21.3, associated with coronary artery disease and type 2 diabetes, respectively.

Similar articles

Cited by

References

    1. Barrett JC, et al. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005;21:263–265. - PubMed
    1. The International HapMap Consortium. A second generation human haplotype map of over 3.1 million SNPs. Nature. 2007;449:851–861. - PMC - PubMed
    1. Helgadottir A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007;316:1491–1493. - PubMed
    1. Liefeld T, et al. GeneCruiser: a web service for the annotation of microarray data. Bioinformatics. 2005;21:3681–3682. - PubMed
    1. 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