Impact of whole genome amplification on analysis of copy number variants
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/36/13/e80/16747513/gkn378.pdf
Reference24 articles.
1. Common deletion polymorphisms in the human genome;McCarroll;Nat. Genet.,2006
2. Structural variation in the human genome;Feuk;Nat. Rev. Genet.,2006
3. A high-resolution survey of deletion polymorphism in the human genome;Conrad;Nat. Genet.,2006
4. Segmental duplications and copy-number variation in the human genome;Sharp;Am. J. Hum. Genet.,2005
5. Detection of large-scale variation in the human genome;Iafrate;Nat. Genet.,2004
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