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

Nucleic acids research - 1 Jan 2006

Packer Bernice R, Yeager Meredith, Burdett Laura, Welch Robert, Beerman Michael, Qi Liqun, Sicotte Hugues, Staats Brian, Acharya Mekhala, Crenshaw Andrew, Eckert Andrew, Puri Vinita, Gerhard Daniela S, Chanock Stephen J

Abstract excerpt

The SNP500Cancer database provides sequence and genotype assay information for candidate SNPs useful in mapping complex diseases, such as cancer. The database is an integral component of the NCI 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:...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 16381944
DOI: 10.1093/nar/gkj151
PMCID: PMC1347513

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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