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  • aquleaf
    Member
    • Mar 2010
    • 38

    multiple mapped reads

    Hi.

    We did RNA paired-end sequencing. After alignment analysis, I found there were such reads. One end were with multiple alignments, while the other end with unique alignment. How to treat these reads? Should I eliminate them before inputting the alignments into Cufflinks or Scriputure?

    Wish your suggestions! Thanks very much in advance?
  • chadn737
    Senior Member
    • Jan 2009
    • 392

    #2
    If one of the paired ends maps uniquely, then the other multi-mapped end would have came from that same transcript. I think you confidently trust that and discard the other regions that the one mapped to.

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    • cedance
      Senior Member
      • Feb 2011
      • 108

      #3
      Yes, that seems to be the consensus. Although I discard this read with multiple hits and consider that unique hit as a single end read (because my library consists of paired end and single end read anyways and so I have to run tophat twice). But it seems perfectly reasonable to consider the solution from chadn737.

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