Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

Determination of copy number variants (CNVs) inferred in genome wide single nucleotide polymorphism arrays has shown increasing utility in genetic variant disease associations. Several CNV detection methods are available, but differences in CNV call thresholds and characteristics exist. We evaluated...

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Detalles Bibliográficos
Autores principales: Dellinger, Andrew E., Saw, Seang-Mei, Goh, Liang K., Seielstad, Mark, Young, Terri L., Li, Yi-Ju
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875020/
https://www.ncbi.nlm.nih.gov/pubmed/20142258
http://dx.doi.org/10.1093/nar/gkq040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875020/
https://www.ncbi.nlm.nih.gov/pubmed/20142258
http://dx.doi.org/10.1093/nar/gkq040

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