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deepSNV

Bioc current

Detection of subclonal SNVs in deep sequencing data.

v1.58.0 · software · GPL-3

Release Lineage

Entered 2.10 · Apr 2, 2012

Current · Requires R 4.6

1.0 In 29 of 49 releases 3.23

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.

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Depended on by (2)

Bioconductor (2)

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