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CNstream: A method for the identification and genotyping of copy number polymorphisms using Illumina microarrays
BACKGROUND: Understanding the genetic basis of disease risk in depth requires an exhaustive knowledge of the types of genetic variation. Very recently, Copy Number Variants (CNVs) have received much attention because of their potential implication in common disease susceptibility. Copy Number Polymo...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3098064/ https://ncbi.nlm.nih.gov/pubmed/20482829 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-264 |
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