Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • laura.benestan
    Junior Member
    • Dec 2012
    • 2

    Unsual peak in a RAD seq library

    Hi all,

    I'm preparing RAD sequencing library with a protocol inspired by Etter et al, except that I use Amplicon Beads instead of a gel.
    Before sending to the sequencing platform I make a High sensitivity DNA chip (AGilent machine) to check the size of my fragment (normally between 300-800 base pairs).
    On most of my samples I got a big peak at about 3000 base pairs, something that I don't understand.

    Firts I thought it was the beads. But, this peak appear only after the PCR step, it is not there before PCR or either after sonication.
    Is there anyone here that had the same problem ?
    Also, some others people had the same problem than I with a different protocol, the GBS one (Elshire et al), but the same machine (Agilent).

    Thanks for your help,

    Laura
  • JackieBadger
    Senior Member
    • Mar 2009
    • 385

    #2
    I havent read that specific protocol but could hazard a guess perhaps. Do the large fragments occur after digestion?
    If so it could be large chimera formation via your sticky ends (if your protocol produces them). I know that this is an issue in the genotyping by sequencing protocol, and in ddRAD. Just modify the protocol and size select as in the ddRAD protocol. Then when you align to a genome you should know the distance between your paired ends. If this is for eg much bigger than expected, this is probably due to chimera formation.

    I am guess taking a guess here
    Last edited by JackieBadger; 12-11-2012, 07:33 PM.

    Comment

    • pmiguel
      Senior Member
      • Aug 2008
      • 2328

      #3
      Originally posted by laura.benestan View Post
      Hi all,

      I'm preparing RAD sequencing library with a protocol inspired by Etter et al, except that I use Amplicon Beads instead of a gel.
      Before sending to the sequencing platform I make a High sensitivity DNA chip (AGilent machine) to check the size of my fragment (normally between 300-800 base pairs).
      On most of my samples I got a big peak at about 3000 base pairs, something that I don't understand.
      Would you post the image, please?

      --
      Phillip

      Comment

      • laura.benestan
        Junior Member
        • Dec 2012
        • 2

        #4
        Thanks for your quick answer.
        Enclosed, there is the Bioanalyser profil displaying an unusual peak at about 3000 bp.


        Those fragments doesn't appear after digestion. We made an agarose gel yesterday and there were no detectable amount of such fragment at 3000bp. It seems to be an artefact....but we still don't understand why this fragment appears only after PCR.

        At the beginning, we also thought that was due to the sticky ends. However, the size of this big fragments is always the same (about 3000bp) whereas we should expect some size variation in this case.
        Attached Files

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM
        • SEQadmin2
          Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
          by SEQadmin2



          Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
          ...
          07-09-2026, 11:10 AM
        • SEQadmin2
          Cancer Drug Resistance: The Lingering Barrier to Rising Survival
          by SEQadmin2



          Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

          There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
          07-08-2026, 05:17 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 07-20-2026, 11:10 AM
        0 responses
        18 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-13-2026, 10:26 AM
        0 responses
        32 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-09-2026, 10:04 AM
        0 responses
        43 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-08-2026, 10:08 AM
        0 responses
        29 views
        0 reactions
        Last Post SEQadmin2  
        Working...