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A comparative analysis of algorithms for somatic SNV detection in cancer
Motivation: With the advent of relatively affordable high-throughput technologies, DNA sequencing of cancers is now common practice in cancer research projects and will be increasingly used in clinical practice to inform diagnosis and treatment. Somatic (cancer-only) single nucleotide variants (SNVs...
Autores principales: | Roberts, Nicola D., Kortschak, R. Daniel, Parker, Wendy T., Schreiber, Andreas W., Branford, Susan, Scott, Hamish S., Glonek, Garique, Adelson, David L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753564/ https://www.ncbi.nlm.nih.gov/pubmed/23842810 http://dx.doi.org/10.1093/bioinformatics/btt375 |
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