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Inference of alternative splicing from RNA-Seq data with probabilistic splice graphs.

Bioinformatics (Oxford, England) | 2013

Alternative splicing and other processes that allow for different transcripts to be derived from the same gene are significant forces in the eukaryotic cell. RNA-Seq is a promising technology for analyzing alternative transcripts, as it does not require prior knowledge of transcript structures or genome sequences. However, analysis of RNA-Seq data in the presence of genes with large numbers of alternative transcripts is currently challenging due to efficiency, identifiability and representation issues.

Pubmed ID: 23846746 RIS Download

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Associated grants

  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG005232
  • Agency: NHGRI NIH HHS, United States
    Id: HG005232

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Bowtie (tool)

RRID:SCR_005476

Software ultrafast memory efficient tool for aligning sequencing reads. Bowtie is short read aligner.

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