Bioconductor version: Release (2.12)
Infer alternative splicing from paired-end RNA-seq data. The model is based on counting paths across exons, rather than pairwise exon connections, and estimates the fragment size and start distributions non-parametrically, which improves estimation precision.
Author: David Rossell, Camille Stephan-Otto, Manuel Kroiss
Maintainer: David Rossell <rosselldavid at gmail.org>
To install this package, start R and enter:
    source("http://bioconductor.org/biocLite.R")
    biocLite("casper")
    To cite this package in a publication, start R and enter:
    citation("casper")
    | R Script | Manual for the casper library | |
| Reference Manual | 
| biocViews | Bioinformatics, DifferentialExpression, GeneExpression, HighThroughputSequencing, RNASeq, Software, Transcription | 
| Version | 1.1.2 | 
| In Bioconductor since | BioC 2.13 (R-2.18) | 
| License | GPL (>=2) | 
| Depends | R (>= 2.14.1), Biobase, IRanges, methods, gtools, GenomicRanges, Rsamtools, plyr, gaga | 
| Imports | VGAM, mgcv, GenomicFeatures, survival, sqldf | 
| Suggests | |
| System Requirements | |
| URL | |
| Depends On Me | |
| Imports Me | |
| Suggests Me | 
| Package Source | casper_1.1.2.tar.gz | 
| Windows Binary | casper_1.1.2.zip (32- & 64-bit) | 
| Mac OS X 10.6 (Snow Leopard) | casper_1.1.2.tgz | 
| Package Downloads Report | Download Stats | 
 
  
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