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.
|Author||Yves Rozenholc, Nicolas Pécuchet, Pierre Laurent-Puig|
|Date of publication||2017-11-15 13:30:36 UTC|
|Maintainer||Yves Rozenholc <[email protected]>|
|License||MIT + file LICENSE|
|Package repository||View on CRAN|
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