Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Vinz
    Member
    • Dec 2010
    • 80

    #1

    Primerdimer/Short Product Bias on the MiSeq

    Primerdimers are more efficient in cluster formation than longer products.
    Our data suggests that the extent of this preference can be influenced by sample preparation after (!) cleanup. Anyone has a guess or even knowledge what step / how one could influence the ratio of primerdimer clusters versus normal size products?
    Denaturing conditions?
    Handling times?
    Temperatures?
    HT1 buffer?

    Background: We experienced that the rate of primerdimer rate is changing over time. In particular we have one example of 8 pools of samples that were cleaned up together but put on different runs. They show a marked difference in primerdimer rate that can not be explained by the nature of the samples.
  • nefertitichen
    Junior Member
    • May 2010
    • 2

    #2
    I would try to get rid of the primer dimers with AMPure beads before pooling for sequencing.

    Comment

    • thomasblomquist
      Member
      • Jul 2012
      • 68

      #3
      Post-PCR cleanup of multiplex amplicon library prep is almost a given. Ampure beads, gel electrophoresis and band cut out, column exclusions, etc, are all decent options for Illumina library prep clean up and removal of primer dimers.

      This is not the same thing as universal multiplex pcr library amplification which has a single primer that amplifies all products that have a common adapter attached on each end.

      That being said, annealing temperature and time is key to minimization primer dimer formation, as well as any sort of off-target priming. There is a direct correlation between the specificity of the priming and annealing temperature. Conversely there is an inverse relationship with cycle-to-cycle yield/efficiency. Another consideration is to back off of primer concentration if specific primers are giving non-specific dimerization products.

      Remember, PCR is a COMPLEX enzymatic reaction, with a lot of potential side reactions if you don't optimize the kinetics favorably for the desired product formation.

      Regards,

      -Tom Blomquist

      Comment

      • snetmcom
        Senior Member
        • Oct 2008
        • 159

        #4
        Pippin Prep
        Ampure Cleanup
        EGel

        It usually takes 2 rounds of cleanup to fully remove most byproducts.
        All of these options will be easier than trying to configure cluster generation.
        Last edited by snetmcom; 02-21-2014, 06:43 PM.

        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, 10:52 AM
        0 responses
        9 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        19 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-13-2026, 09:56 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-09-2026, 11:14 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Working...