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    Banned
    • Feb 2008
    • 1331

    RNA-Seq: TopHat-Fusion: an algorithm for discovery of novel fusion transcripts.

    Syndicated from PubMed RSS Feeds

    TopHat-Fusion: an algorithm for discovery of novel fusion transcripts.

    Genome Biol. 2011 Aug 11;12(8):R72

    Authors: Kim D, Salzberg SL

    ABSTRACT: TopHat-Fusion is an algorithm designed to discover transcripts representing fusion gene products, which result from the breakage and re-joining of two different chromosomes, or from rearrangements within a chromosome. TopHat-Fusion is an enhanced version of TopHat, an efficient program that aligns RNA-seq reads without relying on existing annotation. Because it is independent of gene annotation, TopHat-Fusion can discover fusion products deriving from known genes, unknown genes and unannotated splice variants of known genes. Using RNA-seq data from breast and prostate cancer cell lines, we detected both previously reported and novel fusions with solid supporting evidence. TopHat-Fusion is available at http://tophat-fusion.sourceforge.net/.

    PMID: 21835007 [PubMed - as supplied by publisher]



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  • bharati
    Member
    • Mar 2012
    • 38

    #2
    Confusion between Spanning reads and spanning mate pairs

    Can anybody please explain the difference between Spanning Reads and Spanning Mate pairs. As much I could understand Spanning reads are those reads which do not harbor the fusion point but Split reads do harbor it, but Spanning mate pairs are those spanning reads which are supported by their mate pairs and the number of Spanning mate pairs should be lesser than spanning reads, but this is not the case in my results.

    Comment

    • Charitra
      Member
      • Feb 2013
      • 57

      #3
      can anybody give me guidance on how to select fusion candidate after tophat2-fusion result.html for validation ?

      Comment

      • jp.
        Senior Member
        • Jul 2013
        • 142

        #4
        Finally, I got the answer

        Comment

        • bharati
          Member
          • Mar 2012
          • 38

          #5
          Can u pls explain the ans u got.

          Comment

          • jp.
            Senior Member
            • Jul 2013
            • 142

            #6
            1. check the location and significance of geens
            2. high spanning read
            3. PCR validation

            Comment

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