cnvCapSeq: detecting copy number variation in long-range targeted resequencing data

Targeted resequencing technologies have allowed for efficient and cost-effective detection of genomic variants in specific regions of interest. Although capture sequencing has been primarily used for investigating single nucleotide variants and indels, it has the potential to elucidate a broader spe...

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Detalles Bibliográficos
Autores principales: Bellos, Evangelos, Kumar, Vikrant, Lin, Clarabelle, Maggi, Jordi, Phua, Zai Yang, Cheng, Ching-Yu, Cheung, Chui Ming Gemmy, Hibberd, Martin L., Wong, Tien Yin, Coin, Lachlan J. M., Davila, Sonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227763/
https://www.ncbi.nlm.nih.gov/pubmed/25228465
http://dx.doi.org/10.1093/nar/gku849

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227763/
https://www.ncbi.nlm.nih.gov/pubmed/25228465
http://dx.doi.org/10.1093/nar/gku849

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