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.
- Version1.7.2
- R versionunknown
- LicenseMIT
- Needs compilation?No
- Last release06/11/2018
Team
Yves Rozenholc
Nicolas Pécuchet
Show author detailsRolesAuthorPierre Laurent-Puig
Show author detailsRolesAuthor
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- Depends1 package
- Imports1 package