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  • vpp605
    Junior Member
    • Feb 2009
    • 6

    #1

    Removing Duplicate Reads from Torrent data

    Does anyone have any experience with removing duplicate reads from Ion Torrent data? Any idea if the 454-designed programs work well with Torrent (e.g., cd-hit-454)? Or any suggestions for other programs to use? The basis for this question is PCR-derived duplicates which I am anticipating will skew our analysis, and I would therefore like to remove them.

    I should also mention that we do not have a reference genome to align reads to, as we are working with WGS metagenomic data.
    Last edited by vpp605; 06-10-2013, 06:52 AM.
  • jtackney
    Member
    • May 2012
    • 16

    #2
    Hi - did you ever figure this out?

    I've been using samtools "rmdup -s" but I don't think it's working as advertised for single-end reads of variable length....

    Comment

    • eulbra
      Junior Member
      • Mar 2012
      • 8

      #3
      picard tools can do the job

      Comment

      • IonTorrent
        Member
        • Jan 2010
        • 64

        #4
        Hi there,

        There is functionality within the Torrent Suite software for duplicate read marking, which can be enabled as desired. There is more information available via the Help tool within Torrent Browser or via Ion Community and the Torrent Suite documentation. There is also a FilterDuplicates plugin available as part of Torrent Suite.

        I would also recommend follow up with your local Field Bioinformatics Scientist if you have any questions on these topics.

        Originally posted by vpp605 View Post
        Does anyone have any experience with removing duplicate reads from Ion Torrent data? Any idea if the 454-designed programs work well with Torrent (e.g., cd-hit-454)? Or any suggestions for other programs to use? The basis for this question is PCR-derived duplicates which I am anticipating will skew our analysis, and I would therefore like to remove them.

        I should also mention that we do not have a reference genome to align reads to, as we are working with WGS metagenomic data.

        Comment

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