CoNVEX: copy number variation estimation in exome sequencing data using HMM

BACKGROUND: One of the main types of genetic variations in cancer is Copy Number Variations (CNV). Whole exome sequenicng (WES) is a popular alternative to whole genome sequencing (WGS) to study disease specific genomic variations. However, finding CNV in Cancer samples using WES data has not been f...

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Detalles Bibliográficos
Autores principales: Amarasinghe, Kaushalya C, Li, Jason, Halgamuge, Saman K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549847/
https://www.ncbi.nlm.nih.gov/pubmed/23368785
http://dx.doi.org/10.1186/1471-2105-14-S2-S2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549847/
https://www.ncbi.nlm.nih.gov/pubmed/23368785
http://dx.doi.org/10.1186/1471-2105-14-S2-S2

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