Bioconductor version: Development (2.8)
Provides means of analysis for RNAseq data, used together with genomic annotation from Ensembl. Requires 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 ; Michal Okoniewski
Maintainer: Michal Okoniewski 
To install this package, start R and enter:
source("http:///biocLite.R")
biocLite("rnaSeqMap")    
| R Script | rnaSeqMap primer | 
| biocViews | Annotation, Bioinformatics, ReportWriting, Transcription, GeneExpression, DifferentialExpression, HighThroughputSequencing, RNAseq, SAGE, Visualization | 
| Depends | R, methods, xmapcore | 
| Imports | Biobase, IRanges, edgeR, DESeq, DBI, RMySQL | 
| Suggests | |
| System Requirements | |
| License | GPL-2 | 
| URL | |
| Depends On Me | |
| Imports Me | |
| Suggests Me | |
| Version | 1.1.0 | 
| Package Source | rnaSeqMap_1.1.0.tar.gz | 
| Windows Binary | rnaSeqMap_1.1.0.zip (32- & 64-bit) | 
| MacOS 10.5 (Leopard) binary | rnaSeqMap_1.1.0.tgz | 
| Package Downloads Report | Download Stats | 
 
  
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