PVAAS: identify variants associated with aberrant splicing from RNA-seq

Motivation: RNA-seq has been widely used to study the transcriptome. Comparing to microarray, sequencing-based RNA-seq is able to identify splicing variants and single nucleotide variants in one experiment simultaneously. This provides unique opportunity to detect variants that associated with aberr...

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Bibliographic Details
Published in:Bioinformatics
Main Authors: Wang, Liguo, Nie, Jinfu J., Kocher, Jean-Pierre A.
Format: Artigo
Language:Inglês
Published: Oxford University Press 2015
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Applications Notes
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4807355/
https://ncbi.nlm.nih.gov/pubmed/25573917
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv001
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