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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