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cran
PlasmaMutationDetector:Tumor Mutation Detection in Plasma
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.
Maintained by Yves Rozenholc. Last updated 7 years ago.
1.30 score