Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • 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.

  • #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


    • #3
      picard tools can do the job

      Comment


      • #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

        Latest Articles

        Collapse

        • seqadmin
          Advancing Precision Medicine for Rare Diseases in Children
          by seqadmin




          Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
          12-16-2024, 07:57 AM
        • seqadmin
          Recent Advances in Sequencing Technologies
          by seqadmin



          Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

          Long-Read Sequencing
          Long-read sequencing has seen remarkable advancements,...
          12-02-2024, 01:49 PM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, 12-17-2024, 10:28 AM
        0 responses
        33 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 12-13-2024, 08:24 AM
        0 responses
        49 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 12-12-2024, 07:41 AM
        0 responses
        34 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 12-11-2024, 07:45 AM
        0 responses
        46 views
        0 likes
        Last Post seqadmin  
        Working...
        X