Major copy proportion analysis of tumor samples using SNP arrays

BACKGROUND: Single nucleotide polymorphisms (SNPs) are the most common genetic variations in the human genome and are useful as genomic markers. Oligonucleotide SNP microarrays have been developed for high-throughput genotyping of up to 900,000 human SNPs and have been used widely in linkage and can...

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Detaylı Bibliyografya
Asıl Yazarlar: Li, Cheng, Beroukhim, Rameen, Weir, Barbara A, Winckler, Wendy, Garraway, Levi A, Sellers, William R, Meyerson, Matthew
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2008
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2375907/
https://ncbi.nlm.nih.gov/pubmed/18426588
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-9-204
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