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SNPseek is heavily dependent upon members of the scientific community who make their research data available to the public. On this page we acknowledge publications and groups that helped make SNPseek possible.

References:

Hinds DA, Cox DR, et al. 2005. Whole-genome patterns of common DNA variation in three human populations. Science 307(5712):1072-9.

International HapMap Consortium. 2005. A haplotype map of the human genome. Nature 426(6968):789-96.

International HapMap Consortium. 2003. The International HapMap Project. Nature 426(6968):789-96.

Karolchik D, Baertsch R, et al. 2003. The UCSC Genome Browser Database. Nucl. Acids Res 31(1):51-54.

Taillon-Miller P, Miller RD, Kwok PY, et al. 2004. Linkage Disequilibrium Maps Constructed with Common SNPs are Useful for First-pass Disease Association Screens. Genomics 84(6):899-912.

Acknowledgements:

We thank the International HapMap Consortium for the majority of SNP frequency data, and the UCSC Genome Browser team for genomic annotation data.

SNPseek Citations:

Engle LJ, Simpson CL, Landers JE. 2006. Using high-throughput SNP technologies to study cancer . Oncogene. 25(11):1594-601. Review.

Cheng D, Zhang H, Young N, Damaraju S, Wishart D. 2006. PolySearch: A Web Based System integrating PubMed, Human Genome Data and Primer Design Tools for Management of Pharmacogenomic Projects . Canadian Proteomics Initiative Conference (CPI 2006). Poster.