FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing

Allele-specific copy number analysis (ASCN) from next generation sequencing (NGS) data can greatly extend the utility of NGS beyond the identification of mutations to precisely annotate the genome for the detection of homozygous/heterozygous deletions, copy-neutral loss-of-heterozygosity (LOH), alle...

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Detalles Bibliográficos
Autores principales: Shen, Ronglai, Seshan, Venkatraman E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Methods Online
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027494/
https://www.ncbi.nlm.nih.gov/pubmed/27270079
http://dx.doi.org/10.1093/nar/gkw520

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027494/
https://www.ncbi.nlm.nih.gov/pubmed/27270079
http://dx.doi.org/10.1093/nar/gkw520

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