Bioconductor version: Release (2.7)
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 | 1.0.0 |
| Package Source | rnaSeqMap_1.0.0.tar.gz |
| Windows Binary | rnaSeqMap_1.0.0.zip (32- & 64-bit) |
| MacOS 10.5 (Leopard) binary | rnaSeqMap_1.0.0.tgz |
| Package Downloads Report | Download Stats |
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