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Copy Number Variation in Human Health, Disease, and Evolution
Copy number variation (CNV) is a source of genetic diversity in humans. Numerous CNVs are being identified with various genome analysis platforms, including array comparative genomic hybridization (aCGH), single nucleotide polymorphism (SNP) genotyping platforms, and next-generation sequencing. CNV...
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| Yayımlandı: | Annu Rev Genomics Hum Genet |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2009
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4472309/ https://ncbi.nlm.nih.gov/pubmed/19715442 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1146/annurev.genom.9.081307.164217 |
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