CODEX: a normalization and copy number variation detection method for whole exome sequencing

High-throughput sequencing of DNA coding regions has become a common way of assaying genomic variation in the study of human diseases. Copy number variation (CNV) is an important type of genomic variation, but detecting and characterizing CNV from exome sequencing is challenging due to the high leve...

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Detalles Bibliográficos
Autores principales: Jiang, Yuchao, Oldridge, Derek A., Diskin, Sharon J., Zhang, Nancy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381046/
https://www.ncbi.nlm.nih.gov/pubmed/25618849
http://dx.doi.org/10.1093/nar/gku1363

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381046/
https://www.ncbi.nlm.nih.gov/pubmed/25618849
http://dx.doi.org/10.1093/nar/gku1363

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