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  • kga1978
    Senior Member
    • Nov 2010
    • 100

    #1

    PairedreadFinder or similar?

    Hi,

    I have two fastq files that originated from a matched paired-end library (mate-pair1.fastq and mate-pair2.fastq), but I have now trimmed them and they contain different numbers of reads and are out of sync. Some of the reads have matched pairs, but others don't. Is there a program that can fix this for me? I know 'PairedreadFinder' (part of earlier versions of FAR) can do this, but I can't get this program to work (keep getting 'error while loading shared libraries: libtbb.so.2' even though I copied the required library to the same folder as FAR/PairedreadFinder). I know of a few perl scripts out there but they require a ton of memory and aren't very efficient.

    Any help would be greatly appreciated.
  • sklages
    Senior Member
    • May 2008
    • 628

    #2
    adjust you LD_LIBRARY_PATH to point to the directory containing the library; then the program should work (or give you another error message) ..

    Comment

    • nsl
      Member
      • Jan 2011
      • 28

      #3
      Not sure whether you fixed the problem, but I think you can you can use "Filter SAM" under "SAM TOOLs" in galaxy as an alternative.

      Comment

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