Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

Recent reports indicate that copy number variations (CNVs) within the human genome contribute to nucleotide diversity to a larger extent than single nucleotide polymorphisms (SNPs). In addition, the contribution of CNVs to human disease susceptibility may be greater than previously expected, althoug...

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Detalles Bibliográficos
Autores principales: Komura, Daisuke, Shen, Fan, Ishikawa, Shumpei, Fitch, Karen R., Chen, Wenwei, Zhang, Jane, Liu, Guoying, Ihara, Sigeo, Nakamura, Hiroshi, Hurles, Matthew E., Lee, Charles, Scherer, Stephen W., Jones, Keith W., Shapero, Michael H., Huang, Jing, Aburatani, Hiroyuki
Formato: Artigo
Lenguaje:Inglês
Publicado: Cold Spring Harbor Laboratory Press 2006
Materias:
Methods
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1665641/
https://ncbi.nlm.nih.gov/pubmed/17122084
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.5629106
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