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NADfinder

This is the released version of NADfinder; for the devel version, see NADfinder.

All versions 3.24 (devel), 3.23 (release), 3.22, 3.21, 3.20, 3.19, 3.18, 3.17, 3.16, 3.15, 3.14, 3.13, 3.12, 3.11, 3.10, 3.9, 3.8, 3.7, 3.6, 3.5

Call wide peaks for sequencing data


Bioconductor version: Release (3.23)

Nucleolus is an important structure inside the nucleus in eukaryotic cells. It is the site for transcribing rDNA into rRNA and for assembling ribosomes, aka ribosome biogenesis. In addition, nucleoli are dynamic hubs through which numerous proteins shuttle and contact specific non-rDNA genomic loci. Deep sequencing analyses of DNA associated with isolated nucleoli (NAD- seq) have shown that specific loci, termed nucleolus- associated domains (NADs) form frequent three- dimensional associations with nucleoli. NAD-seq has been used to study the biological functions of NAD and the dynamics of NAD distribution during embryonic stem cell (ESC) differentiation. Here, we developed a Bioconductor package NADfinder for bioinformatic analysis of the NAD-seq data, including baseline correction, smoothing, normalization, peak calling, and annotation.

Author: Jianhong Ou, Haibo Liu, Jun Yu, Hervé Pagès, Paul Kaufman, Lihua Julie Zhu

Maintainer: Jianhong Ou <jou at morgridge.org>, Lihua Julie Zhu <julie.zhu at umassmed.edu>

Citation (from within R, enter citation("NADfinder")):

Jianhong Ou, Haibo Liu, Jun Yu, Hervé Pagès, Paul Kaufman, Lihua Julie Zhu. NADfinder: Call wide peaks for sequencing data. doi:10.18129/B9.bioc.NADfinder, R package version 1.36.0, https://bioconductor.org/packages/NADfinder.

Generated from the package metadata; it may differ from the package's own citation.

Installation

To install this package, start R (version "4.6") and enter:

if (!require("BiocManager", quietly = TRUE))
    install.packages("BiocManager")

BiocManager::install("NADfinder")

For older versions of R, please refer to the appropriate Bioconductor release.

Documentation

To view documentation for the version of this package installed in your system, start R and enter:

browseVignettes("NADfinder")
NADfinder.html HTML R Script
Reference ManualPDF
NEWSText

Details

biocViews DNASeq, GeneRegulation, PeakDetection, Sequencing, Software
Version1.36.0
In Bioconductor sinceBioC 3.5 (R-3.4) (9.5 years)
License GPL (>= 2)
Depends R (>= 3.5.0), BiocGenerics, IRanges, GenomicRanges, S4Vectors, SummarizedExperiment
Imports graphics, methods, baseline, signal, GenomicAlignments, GenomeInfoDb, rtracklayer, limma, trackViewer, stats, utils, Rsamtools, metap, EmpiricalBrownsMethod, ATACseqQC, corrplot, csaw
System Requirements
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Suggests RUnit, BiocStyle, knitr, BSgenome.Mmusculus.UCSC.mm10, testthat, BiocManager, rmarkdown
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Package Archives

Follow Installation instructions to use this package in your R session.

Source Package NADfinder_1.36.0.tar.gz
Windows Binary (x86_64) NADfinder_1.36.0.zip
macOS Binary (big-sur-x86_64) NADfinder_1.36.0.tgz
macOS Binary (sonoma-arm64) NADfinder_1.36.0.tgz
Source Repositorygit clone https://git.bioconductor.org/packages/NADfinder
Source Repository (Developer Access)git clone git@git.bioconductor.org:packages/NADfinder
Package Short Url https://bioconductor.org/packages/NADfinder/
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