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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Detalles Bibliográficos
Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347513/
https://www.ncbi.nlm.nih.gov/pubmed/16381944
http://dx.doi.org/10.1093/nar/gkj151

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347513/
https://www.ncbi.nlm.nih.gov/pubmed/16381944
http://dx.doi.org/10.1093/nar/gkj151

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