A carregar...

Copy number variation detection and genotyping from exome sequence data

While exome sequencing is readily amenable to single-nucleotide variant discovery, the sparse and nonuniform nature of the exome capture reaction has hindered exome-based detection and characterization of genic copy number variation. We developed a novel method using singular value decomposition (SV...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Krumm, Niklas, Sudmant, Peter H., Ko, Arthur, O'Roak, Brian J., Malig, Maika, Coe, Bradley P., Quinlan, Aaron R., Nickerson, Deborah A., Eichler, Evan E.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3409265/
https://ncbi.nlm.nih.gov/pubmed/22585873
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.138115.112
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!