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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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| Publicado en: | Nucleic Acids Res |
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| Autores principales: | , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Oxford University Press
2016
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| Materias: | |
| Acceso en línea: | 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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