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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.
Package details |
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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 <mertes@in.tum.de> |
License | MIT + file LICENSE |
Version | 1.2.1 |
URL | https://github.com/gagneurlab/FRASER |
Package repository | View on Bioconductor |
Installation |
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