Copy number variation and human genome maps
- PMID: 20428091
- DOI: 10.1038/ng0510-365
Copy number variation and human genome maps
Abstract
Maps of human genome copy number variation (CNV) are maturing into useful resources for complex disease genetics. Four new studies increase the resolution of CNV maps and seek to locate human phenotypic variation on these maps.
Comment on
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Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.Nat Genet. 2010 May;42(5):385-91. doi: 10.1038/ng.564. Epub 2010 Apr 4. Nat Genet. 2010. PMID: 20364136 Free PMC article.
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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing.Nat Genet. 2010 May;42(5):400-5. doi: 10.1038/ng.555. Epub 2010 Apr 4. Nat Genet. 2010. PMID: 20364138 Free PMC article.
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