CODEX: a normalization and copy number variation detection method for whole exome sequencing
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/43/6/e39/17434109/gku1363.pdf
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4. Genome assembly comparison identifies structural variants in the human genome;Khaja;Nat. Genet.,2006
5. Copy number variation at 1q21.1 associated with neuroblastoma;Diskin;Nature,2009
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