This package is for version 3.12 of Bioconductor; for the stable, up-to-date release version, see deepSNV.
Bioconductor version: 3.12
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.
Author: Niko Beerenwinkel [ths], Raul Alcantara [ctb], David Jones [ctb], Inigo Martincorena [ctb], Moritz Gerstung [aut, cre]
Maintainer: Moritz Gerstung <moritz.gerstung at ebi.ac.uk>
Citation (from within R,
enter citation("deepSNV")
):
To install this package, start R (version "4.0") and enter:
if (!requireNamespace("BiocManager", quietly = TRUE)) install.packages("BiocManager") BiocManager::install("deepSNV")
For older versions of R, please refer to the appropriate Bioconductor release.
To view documentation for the version of this package installed in your system, start R and enter:
browseVignettes("deepSNV")
R Script | An R package for detecting low frequency variants in deep sequencing experiments | |
HTML | R Script | Shearwater ML |
R Script | Subclonal variant calling with multiple samples and prior knowledge using shearwater | |
Reference Manual | ||
Text | NEWS |
biocViews | DataImport, GeneticVariability, Genetics, SNP, Sequencing, Software |
Version | 1.36.0 |
In Bioconductor since | BioC 2.10 (R-2.15) (9 years) |
License | GPL-3 |
Depends | R (>= 2.13.0), methods, graphics, parallel, IRanges, GenomicRanges, SummarizedExperiment, Biostrings, VGAM, VariantAnnotation(>= 1.13.44) |
Imports | Rhtslib |
LinkingTo | Rhtslib(>= 1.13.1) |
Suggests | RColorBrewer, knitr, rmarkdown |
SystemRequirements | GNU make |
Enhances | |
URL | |
Depends On Me | |
Imports Me | |
Suggests Me | GenomicFiles |
Links To Me | |
Build Report |
Follow Installation instructions to use this package in your R session.
Source Package | deepSNV_1.36.0.tar.gz |
Windows Binary | deepSNV_1.36.0.zip (32- & 64-bit) |
macOS 10.13 (High Sierra) | deepSNV_1.36.0.tgz |
Source Repository | git clone https://git.bioconductor.org/packages/deepSNV |
Source Repository (Developer Access) | git clone git@git.bioconductor.org:packages/deepSNV |
Package Short Url | https://bioconductor.org/packages/deepSNV/ |
Package Downloads Report | Download Stats |
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