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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Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: Cold Spring Harbor Laboratory Press 2006
Teme:
Methods
Online pristup: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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