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.
Version: |
1.7.2 |
Depends: |
R (≥ 3.4.0), ggplot2 (≥ 2.2.0), grid (≥ 3.4.0), GenomicRanges (≥ 1.30.0), VariantAnnotation (≥ 1.24.0) |
Imports: |
S4Vectors (≥ 0.16.0), Rsamtools (≥ 1.30.0), rtracklayer (≥
1.38.0), robustbase (≥ 0.92-8), SummarizedExperiment (≥
1.8.0) |
Published: |
2018-06-11 |
DOI: |
10.32614/CRAN.package.PlasmaMutationDetector |
Author: |
Yves Rozenholc, Nicolas Pécuchet, Pierre Laurent-Puig |
Maintainer: |
Yves Rozenholc <yves.rozenholc at parisdescartes.fr> |
License: |
MIT + file LICENSE |
NeedsCompilation: |
no |
CRAN checks: |
PlasmaMutationDetector results |
Documentation:
Downloads:
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