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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Detalhes bibliográficos
Main Authors: 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
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2006
Assuntos:
Methods
Acesso em linha: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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