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  • Sergio.pv
    Member
    • Jul 2013
    • 21

    #1

    min length and max length with fastx tookit

    Hello everyone,
    i was wondering if there's a way to filter fastq reads based on minimun and maximun length. Plus trimming at minimun quality value.

    this is the closest i've came out with:

    fastq_quality_trimmer -v -t 20 -l 16 -i myfile.fastq -o myfile.trimmed -Q 33

    however, no option to choose the maximun length appears to exists. Is it possible that there are hidden commands that i don't know about (such as -Q 33). According to a technical note from ion torrent, there is an option to limit the maximimun length and it's contained in fastq_quality_trimmer.

    I would greatly appretiate the help,
    Best regards!
    Attached Files
    Last edited by Sergio.pv; 11-19-2013, 12:48 PM.
  • lindenb
    Senior Member
    • Apr 2010
    • 143

    #2
    cross posted on biostars: http://www.biostars.org/p/86850/

    Comment

    • Sergio.pv
      Member
      • Jul 2013
      • 21

      #3
      Yes, that was I.
      I am really stuck with this problem, so i postd it in both sites.

      Best!

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        Curious as to why you need to limit the maximum length?

        Comment

        • Sergio.pv
          Member
          • Jul 2013
          • 21

          #5
          As suggested by the ion torrent's technical note, this would leave little or no adapter sequence in the reads.
          I have attached the mentioned note.

          Comment

          • dpryan
            Devon Ryan
            • Jul 2011
            • 3478

            #6
            It's usually good to mention in this context that you're looking at miRNAs or other short RNAs. At least I assume that's what you're doing since this is specifically mentioned only for miRNA-seq. I (and likely others) would argue that simply quality and adapter trimming should still suffice (just decrease the overlap threshold for the adapter sequence if you want to be more conservative).

            Comment

            • Sergio.pv
              Member
              • Jul 2013
              • 21

              #7
              yes you are right.
              My attempt is to analize data from the <200 nt RNA fraction, to find the most expressed miRNA candidates.

              Best!

              Comment

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