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

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 (). SNP500Cancer reports sequence analysis of anonymized control DNA sample...

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Bibliografiske detaljer
Main Authors: 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.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2006
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1347513/
https://ncbi.nlm.nih.gov/pubmed/16381944
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkj151
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