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

The SNP500Cancer Database provides sequence and genotype assay information for candidate single nucleotide polymorphisms (SNPs) useful in mapping complex diseases, such as cancer. The database is an integral component of the NCI’s Cancer Genome Anatomy Project. SNP500Cancer provides bi-directional s...

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Bibliografische gegevens
Hoofdauteurs: Packer, Bernice R., Yeager, Meredith, Staats, Brian, Welch, Robert, Crenshaw, Andrew, Kiley, Maureen, Eckert, Andrew, Beerman, Michael, Miller, Edward, Bergen, Andrew, Rothman, Nathaniel, Strausberg, Robert, Chanock, Stephen J.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2004
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Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC308740/
https://ncbi.nlm.nih.gov/pubmed/14681474
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkh005
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