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SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes

  1. Author:
    Packer, B. R.
    Yeager, M.
    Burdett, L.
    Welch, R.
    Beerman, M.
    Qi, L. Q.
    Sicotte, H.
    Staats, B.
    Acharya, M.
    Crenshaw, A.
    Eckert, A.
    Puri, V.
    Gerhard, D. S.
    Chanock, S. J.

  2. Author Address

    NCI, Intramural Res Support Program, SAIC Frederick, FCRRDC, Frederick, MD 21701 USA. NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA. George Mason Univ, Dept Bioinformat, Manassas, VA USA. NCI, Off Canc Genom, Bethesda, MD 20892 USA. NCI, Sect Genom Variat, Pediat Oncol Branch, NIH, Gaithersburg, MD USA.;Packer, BR, NCI, Intramural Res Support Program, SAIC Frederick, FCRRDC, Frederick, MD 21701 USA.;packerb@mail.nih.gov
    1. Year: 2006
    2. Date: Jan
  2. Journal: Nucleic Acids Research
    1. 34
    2. Pages: D617-D621
  4. Type of Article: Article
  5. ISSN: 0305-1048
  1. Abstract:

    The SNP500Cancer database provides sequence and genotype assay information for candidate SNPs useful inmapping complex diseases, such as cancer. The database is an integral component of the NCl Cancer Genome Anatomy Project (http://cgap.nci.nih.gov). SNP500Cancer reports sequence analysis of anonymized control DNA samples (n = 102 Coriell samples representing four self-described ethnic groups: African/African-American, Caucasian, Hispanic and Pacific Rim). The website is searchable by gene, chromosome, gene ontology pathway, dbSNP ID and SNP500Cancer SNP ID. As of October 2005, the database contains > 13 400 SNPs, 9124 of which have been sequenced in the SNP500Cancer population. For each analysed SNP, gene location and > 200 bp of surrounding annotated sequence (including nearby SNPs) are provided, with frequency information in total and per subpopulation as well as calculation of Hardy-Weinberg equilibrium for each subpopulation. The website provides the conditions for validated sequencing and genotyping assays, as well as genotype results for the 102 samples, in both viewable and downloadable formats. A subset of sequence validated SNPs with minor allele frequency > 5% are entered into a high-throughput pipeline for genotyping analysis to determine concordance for the same 102 samples. In addition, the results of genotype analysis for select validated SNP assays (defined as 100% concordance between sequence analysis and genotype results) are posted for an additional 280 samples drawn from the Human Diversity Panel (HDP). SNP500Cancer provides an invaluable resource for investigators to select SNPs for analysis, design genotyping assays using validated sequence data, choose selected assays already validated on one or more genotyping platforms, and select reference standards for genotyping assays. The SNP500Cancer database is freely accessible via the web page at http://snp500cancer.nci.nih.gov.

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External Sources

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  2. DOI: 10.1093/nar/gkj151
  3. View record in Web of Science®
  4. WOS: 000239307700131

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