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Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny

SUMMARY: Copy number variation is an important and abundant source of variation in the human genome, which has been associated with a number of diseases, especially cancer. Massively parallel next-generation sequencing allows copy number profiling with fine resolution. Such efforts, however, have me...

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Publicado en:Bioinformatics
Autores principales: Urrutia, Eugene, Chen, Hao, Zhou, Zilu, Zhang, Nancy R, Jiang, Yuchao
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2018
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC6248831/
https://ncbi.nlm.nih.gov/pubmed/29415173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty057
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