Detection, Imputation, and Association Analysis of Small Deletions and Null Alleles on Oligonucleotide Arrays

Copy-number variation (CNV) is a major contributor to human genetic variation. Recently, CNV associations with human disease have been reported. Many genome-wide association (GWA) studies in complex diseases have been performed with sets of biallelic single-nucleotide polymorphisms (SNPs), but the a...

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Detalhes bibliográficos
Principais autores: Franke, Lude, de Kovel, Carolien G.F., Aulchenko, Yurii S., Trynka, Gosia, Zhernakova, Alexandra, Hunt, Karen A., Blauw, Hylke M., van den Berg, Leonard H., Ophoff, Roel, Deloukas, Panagiotis, van Heel, David A., Wijmenga, Cisca
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Human Genetics 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2427186/
https://ncbi.nlm.nih.gov/pubmed/18519066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2008.05.008
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