Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV

Motivation: The ability to detect copy-number variation (CNV) and loss of heterozygosity (LOH) from exome sequencing data extends the utility of this powerful approach that has mainly been used for point or small insertion/deletion detection. Results: We present ExomeCNV, a statistical method to det...

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Autors principals: Sathirapongsasuti, Jarupon Fah, Lee, Hane, Horst, Basil A. J., Brunner, Georg, Cochran, Alistair J., Binder, Scott, Quackenbush, John, Nelson, Stanley F.
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2011
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Original Papers
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3179661/
https://ncbi.nlm.nih.gov/pubmed/21828086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr462
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