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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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Detalhes bibliográficos
Publicado no:Nucleic Acids Res
Main Authors: Shen, Ronglai, Seshan, Venkatraman E.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5027494/
https://ncbi.nlm.nih.gov/pubmed/27270079
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkw520
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