deepSNV
Bioc currentDetection of subclonal SNVs in deep sequencing data.
Release Lineage
Entered 2.10 · Apr 2, 2012
Current · Requires R 4.6
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.
Code
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Topics
Depended on by (2)
Bioconductor (2)
People
- Moritz Gerstung author maintainer
- Raul Alcantara contributor
- Niko Beerenwinkel ths
- David Jones contributor
- John Marshall contributor
- Inigo Martincorena contributor