Package: deepSNV
Maintainer: Moritz Gerstung <moritz.gerstung@ebi.ac.uk>
License: GPL-3
Title: Detection of subclonal SNVs in deep sequencing data.
biocViews: GeneticVariability, SNP, Sequencing, Genetics, DataImport
LinkingTo: Rhtslib (>= 1.13.1)
Type: Package
LazyLoad: yes
Authors@R: c( person("Niko","Beerenwinkel", role="ths"),
    person("David", "Jones", role = "ctb"),
    person("Inigo", "Martincorena", role = "ctb"),
    person("Moritz","Gerstung",
    email = "moritz.gerstung@ebi.ac.uk", role= c("aut","cre")) )
Description: This package provides provides quantitative variant callers for
    detecting subclonal mutations in ultra-deep (>=100x coverage) sequencing
    experiments. The deepSNV algorithm is used for a comparative setup with a
    control experiment of the same loci and uses a beta-binomial model and a
    likelihood ratio test to discriminate sequencing errors and subclonal SNVs.
    The shearwater algorithm computes a Bayes classifier based on a
    beta-binomial model for variant calling with multiple samples for
    precisely estimating model parameters - such as local error rates and
    dispersion - and prior knowledge, e.g. from variation data bases such as
    COSMIC.
Version: 1.28.0
URL: http://github.com/gerstung-lab/deepSNV
Depends: R (>= 2.13.0), methods, graphics, parallel, Rhtslib, IRanges,
        GenomicRanges, SummarizedExperiment, Biostrings, VGAM,
        VariantAnnotation (>= 1.13.44),
Imports: Rhtslib
Suggests: RColorBrewer, knitr, rmarkdown
VignetteBuilder: knitr
RoxygenNote: 6.0.1
git_url: https://git.bioconductor.org/packages/deepSNV
git_branch: RELEASE_3_8
git_last_commit: 9b6d747
git_last_commit_date: 2018-10-30
Date/Publication: 2018-10-30
NeedsCompilation: yes
Packaged: 2018-10-31 01:48:07 UTC; biocbuild
Author: Niko Beerenwinkel [ths],
  David Jones [ctb],
  Inigo Martincorena [ctb],
  Moritz Gerstung [aut, cre]
Built: R 3.5.1; i386-w64-mingw32; 2018-10-31 11:00:00 UTC; windows
Archs: i386, x64
