PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Comprehensive identification and cataloging of copy number variations (CNVs) is required to provide a complete view of human genetic variation. The resolution of CNV detection in previous experimental designs has been limited to tens or hundreds of kilobases. Here we present PennCNV, a hidden Markov...

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Main Authors: Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja
Formato: Artigo
Idioma:Inglês
Publicado: Cold Spring Harbor Laboratory Press 2007
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Methods
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2045149/
https://ncbi.nlm.nih.gov/pubmed/17921354
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.6861907
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