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.
Package details |
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Bioconductor views | DataImport GeneticVariability Genetics SNP Sequencing |
Maintainer | Moritz Gerstung <moritz.gerstung@ebi.ac.uk> |
License | GPL-3 |
Version | 1.43.6 |
Package repository | View on GitHub |
Installation |
Install the latest version of this package by entering the following in R:
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