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Copy number variation signature to predict human ancestry
BACKGROUND: Copy number variations (CNVs) are genomic structural variants that are found in healthy populations and have been observed to be associated with disease susceptibility. Existing methods for CNV detection are often performed on a sample-by-sample basis, which is not ideal for large datase...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598683/ https://www.ncbi.nlm.nih.gov/pubmed/23270563 http://dx.doi.org/10.1186/1471-2105-13-336 |