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, Miranda Stobbe, Victor Pena|
|Bioconductor views||DifferentialExpression GeneExpression RNASeq Sequencing Transcription|
|Maintainer||David Rossell <[email protected]>|
|Package repository||View on Bioconductor|
Install the latest version of this package by entering the following in R:
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.