Bioconductor version: 2.9
Provides means of analysis for RNAseq data, used together with genomic annotation. Requires a set of BAM files on the input or alternatively, an xmapcore database in MySQL as a back-end, which is also a storage for sequencing reads. Front-end analyses include transformations of the coverage function, splicing analysis, finding irreducible regions with the two-sliding-windows algorithm and genomic region visualizations.
Author: Anna Lesniewska <alesniewska at cs.put.poznan.pl>; Michal Okoniewski <michal at fgcz.ethz.ch>
Maintainer: Michal Okoniewski <michal at fgcz.ethz.ch>
To install this package, start R and enter:
source("http://bioconductor.org/biocLite.R") biocLite("rnaSeqMap")
To cite this package in a publication, start R and enter:
citation("rnaSeqMap")
R Script | rnaSeqMap primer | |
Reference Manual |
biocViews | Annotation, Bioinformatics, ReportWriting, Transcription, GeneExpression, DifferentialExpression, HighThroughputSequencing, RNAseq, SAGE, Visualization |
Depends | R (>= 2.11.0), methods, xmapcore, Biobase, Rsamtools |
Imports | GenomicRanges, IRanges, edgeR, DESeq, DBI, RMySQL (>= 0.6-0) |
Suggests | |
System Requirements | |
License | GPL-2 |
URL | |
Depends On Me | |
Imports Me | |
Suggests Me | |
Version | 2.8.0 |
Since | Bioconductor 2.7 (R-2.12) |
Package Source | rnaSeqMap_2.8.0.tar.gz |
Windows Binary | |
MacOS 10.5 (Leopard) binary | rnaSeqMap_2.8.0.tgz |
Package Downloads Report | Download Stats |
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