Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ymc
    Senior Member
    • Mar 2010
    • 496

    #1

    Remove duplicates for differential expression with PE reads?

    Is there a consensus now whether we should remove duplicates for PE reads?

    I think for SE reads, removal is no good because of higher ratio of true duplicates to PCR duplicates.

    PE reads should have a lower ratio but is it low enough to warrant duplicates removal???

    Thanks in advance!
  • Brian Bushnell
    Super Moderator
    • Jan 2014
    • 2709

    #2
    You should never remove duplicates if you did not PCR-amplify. You should not amplify data that you want to measure quantitatively. Ergo, you should not remove duplicates for quantitative studies, because all duplicates are biological for unamplified data.

    That said - if your data is amplified, you should just hope it all amplified about the same and still not remove duplicates. The purpose of removing duplicates is to eliminate non-independent observations of an event when doing variant-calling, as variant-callers will generally assume that the events you feed them are independent and calculate probabilities accordingly.

    And yes, I would never suggest duplicate removal from SE data.

    Comment

    • ymc
      Senior Member
      • Mar 2010
      • 496

      #3
      Originally posted by Brian Bushnell View Post
      You should never remove duplicates if you did not PCR-amplify. You should not amplify data that you want to measure quantitatively. Ergo, you should not remove duplicates for quantitative studies, because all duplicates are biological for unamplified data.

      That said - if your data is amplified, you should just hope it all amplified about the same and still not remove duplicates. The purpose of removing duplicates is to eliminate non-independent observations of an event when doing variant-calling, as variant-callers will generally assume that the events you feed them are independent and calculate probabilities accordingly.

      And yes, I would never suggest duplicate removal from SE data.
      Thank you very much for your detailed reply.

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
        by SEQadmin2



        Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

        Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
        ...
        10-14-2026, 09:55 AM
      • SEQadmin2
        New Genomics Technologies Take Aim at Long-Standing Limits
        by SEQadmin2


        Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

        We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
        ...
        09-28-2026, 10:25 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 11:13 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, Yesterday, 10:48 AM
      0 responses
      15 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      35 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      42 views
      0 reactions
      Last Post SEQadmin2  
      Working...