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ABSTRACT: Motivation
Identification of genomic regions of interest in ChIP-seq data, commonly referred to as peak-calling, aims to find the locations of transcription factor binding sites, modified histones or nucleosomes. The BayesPeak algorithm was developed to model the data structure using Bayesian statistical techniques and was shown to be a reliable method, but did not have a full-genome implementation.Results
In this note we present BayesPeak, an R package for genome-wide peak-calling that provides a flexible implementation of the BayesPeak algorithm and is compatible with downstream BioConductor packages. The BayesPeak package introduces a new method for summarizing posterior probability output, along with methods for handling overfitting and support for parallel processing. We briefly compare the package with other common peak-callers.Availability
Available as part of BioConductor version 2.6. URL: http://bioconductor.org/packages/release/bioc/html/BayesPeak.html.
SUBMITTER: Cairns J
PROVIDER: S-EPMC3042177 | biostudies-literature | 2011 Mar
REPOSITORIES: biostudies-literature
Cairns Jonathan J Spyrou Christiana C Stark Rory R Smith Mike L ML Lynch Andy G AG Tavaré Simon S
Bioinformatics (Oxford, England) 20110117 5
<h4>Motivation</h4>Identification of genomic regions of interest in ChIP-seq data, commonly referred to as peak-calling, aims to find the locations of transcription factor binding sites, modified histones or nucleosomes. The BayesPeak algorithm was developed to model the data structure using Bayesian statistical techniques and was shown to be a reliable method, but did not have a full-genome implementation.<h4>Results</h4>In this note we present BayesPeak, an R package for genome-wide peak-calli ...[more]