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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2006
Pynciau:
Article
Mynediad Ar-lein: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
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg