GenomicAlignments

This package is for version 3.6 of Bioconductor; for the stable, up-to-date release version, see GenomicAlignments.

Representation and manipulation of short genomic alignments

Bioconductor version: 3.6

Provides efficient containers for storing and manipulating short genomic alignments (typically obtained by aligning short reads to a reference genome). This includes read counting, computing the coverage, junction detection, and working with the nucleotide content of the alignments.

Author: Hervé Pagès, Valerie Obenchain, Martin Morgan

Maintainer: Bioconductor Package Maintainer <maintainer at bioconductor.org>

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

Installation

To install this package, start R (version "3.4") and enter:


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

BiocManager::install("GenomicAlignments")

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("GenomicAlignments")

An Introduction to the GenomicAlignments Package	PDF	R Script
Counting reads with summarizeOverlaps	PDF	R Script
Overlap encodings	PDF	R Script
Working with aligned nucleotides	PDF	R Script
Reference Manual	PDF
NEWS	Text
Reading from a BAM file - Part 1	Video
Reading from a BAM file - Part 2	Video

Need some help? Ask on the Bioconductor Support site!

Details

biocViews	Alignment, Coverage, DataImport, Genetics, Infrastructure, RNASeq, SNP, Sequencing, Software
Version	1.14.2
In Bioconductor since	BioC 2.14 (R-3.1) (10 years)
License	Artistic-2.0
Depends	R (>= 2.10), methods, BiocGenerics(>= 0.15.3), S4Vectors(>= 0.13.13), IRanges(>= 2.11.16), GenomeInfoDb(>= 1.13.1), GenomicRanges(>= 1.29.14), SummarizedExperiment(>= 1.5.3), Biostrings(>= 2.37.1), Rsamtools(>= 1.21.4)
Imports	methods, utils, stats, BiocGenerics, S4Vectors, IRanges, GenomicRanges, Biostrings, Rsamtools, BiocParallel
System Requirements
URL

Suggests	ShortRead, rtracklayer, BSgenome, GenomicFeatures, RNAseqData.HNRNPC.bam.chr14, pasillaBamSubset, TxDb.Hsapiens.UCSC.hg19.knownGene, TxDb.Dmelanogaster.UCSC.dm3.ensGene, BSgenome.Dmelanogaster.UCSC.dm3, BSgenome.Hsapiens.UCSC.hg19, DESeq2, edgeR, RUnit, BiocStyle
Linking To	S4Vectors, IRanges
Enhances
Depends On Me	AllelicImbalance, Basic4Cseq, BasicSTARRseq, chimera, ChIPexoQual, exomePeak, GoogleGenomics, groHMM, Guitar, HelloRanges, hiReadsProcessor, prebs, recoup, RIPSeeker, rnaSeqMap, ShortRead, SplicingGraphs
Imports Me	alpine, AneuFinder, ASpli, ATACseqQC, BaalChIP, biovizBase, chimeraviz, ChIPpeakAnno, ChIPQC, chromstaR, CNEr, contiBAIT, CopywriteR, CoverageView, CrispRVariants, customProDB, derfinder, DiffBind, easyRNASeq, FourCSeq, FunChIP, gcapc, GenoGAM, genomation, GenomicFiles, ggbio, gmapR, GreyListChIP, GUIDEseq, Gviz, HTSeqGenie, IMAS, INSPEcT, IntEREst, leeBamViews, MADSEQ, metagene, methylPipe, mosaics, msgbsR, NADfinder, PICS, QuasR, ramwas, Rcade, Repitools, RiboProfiling, RNAprobR, roar, Rqc, rtracklayer, seqplots, SGSeq, soGGi, SplicingGraphs, SPLINTER, TarSeqQC, TCseq, trackViewer, transcriptR, TSRchitect
Suggests Me	alpineData, BiocParallel, gage, GenomeInfoDb, GenomicDataCommons, GenomicFeatures, GenomicRanges, IRanges, oneChannelGUI, parathyroidSE, RNAseqData.HNRNPC.bam.chr14, RnaSeqTutorial, Rsamtools, similaRpeak, Streamer
Links To Me
Build Report	Build Report

Package Archives

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

Source Package	GenomicAlignments_1.14.2.tar.gz
Windows Binary	GenomicAlignments_1.14.2.zip (32- & 64-bit)
Mac OS X 10.11 (El Capitan)	GenomicAlignments_1.14.2.tgz
Source Repository	git clone https://git.bioconductor.org/packages/GenomicAlignments
Source Repository (Developer Access)	git clone git@git.bioconductor.org:packages/GenomicAlignments
Package Short Url	https://bioconductor.org/packages/GenomicAlignments/
Package Downloads Report	Download Stats
Old Source Packages for BioC 3.6	Source Archive