Detection of rare aberrant splicing events in transcriptome profiles. The workflow aims to assist the diagnostics in the field of rare diseases where RNA-seq is performed to identify aberrant splicing defects.
|Author||Christian Mertes [aut, cre], Ines Scheller [aut], Vicente Yepez [ctb], Julien Gagneur [aut]|
|Bioconductor views||AlternativeSplicing Coverage Genetics RNASeq Sequencing Software|
|Maintainer||Christian Mertes <firstname.lastname@example.org>|
|License||MIT + file LICENSE|
|Package repository||View on Bioconductor|
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