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Aims at detecting single nucleotide variation (SNV) and insertion/deletion (INDEL) in circulating tumor DNA (ctDNA), used as a surrogate marker for tumor, at each base position of an Next Generation Sequencing (NGS) analysis. Mutations are assessed by comparing the minor-allele frequency at each position to the measured PER in control samples.
Package details |
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Author | Yves Rozenholc, Nicolas Pécuchet, Pierre Laurent-Puig |
Maintainer | Yves Rozenholc <yves.rozenholc@parisdescartes.fr> |
License | MIT + file LICENSE |
Version | 1.7.2 |
Package repository | View on CRAN |
Installation |
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