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Association tests and software for copy number variant data
Recent studies have suggested that copy number variation (CNV) significantly contributes to genetic predisposition to several common disorders. These findings, combined with the imperfect tagging of CNVs by single nucleotide polymorphisms (SNPs), have motivated the development of association studies...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3525277/ https://ncbi.nlm.nih.gov/pubmed/19164094 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-7364-3-2-191 |
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