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  • Kitty
    Member
    • Jul 2011
    • 10

    #1

    Nextera Problem: Odd fragment size after gel selection

    Hi guys, I'm constructing a PE library by using the Nextera DNA library Prep Kit (Illumina compatible). However, when I cut down the 300-350bp, 450-500bp, 600-650bp region separately after 2.0% agarose gel electrophoresis, there comes double peaks instead of a single narrow peak (pictures). I'm sure there's no problem during gel selection, but obviously, this cannot meet the requirement of a PE library. Is there anyone who has some ideas on this?

    Start with 150ng gDNA, and after 10 cycles of PCR:
    Click image for larger version

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    gel selection 300-350bp:
    Click image for larger version

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    gel selection 450-500bp:
    Click image for larger version

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    gel selection 600-650bp:
    Click image for larger version

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  • pmiguel
    Senior Member
    • Aug 2008
    • 2328

    #2
    Hi Kitty,
    This is a very common issue with Illumina libraries. The good news is that your libraries are probably fine.
    We sometimes just denature the libraries and run them on an RNA chip to determine their size, etc. Info on how to do that here:

    Bridged amplification & clustering followed by sequencing by synthesis. (Genome Analyzer / HiSeq / MiSeq)


    As to what causes the issue exactly, I think it is not completely clear. But probably either the fragments are annealing end-to-end (adapter-to-adapter) forming daisy chains of amplicons, or adapters on both sides of otherwise unrelated amplicons are annealing after denaturation ("bubble products"). More discussion of the possibilities here:

    Bridged amplification & clustering followed by sequencing by synthesis. (Genome Analyzer / HiSeq / MiSeq)


    --
    Phillip

    Comment

    • Kitty
      Member
      • Jul 2011
      • 10

      #3
      Hi Phillip,
      I think you're right, and I'll try to check it on an RNA chip.
      Well, as far as I know, when we loading the library on the Illumina flow cell, there will be a denature step before bridge PCR. So does that mean the "daisy chains" will be separated and may not disturb the output data (insert size distribution)?

      Comment

      • pmiguel
        Senior Member
        • Aug 2008
        • 2328

        #4
        Yes. The problem is mainly that the multimers interfere with determining the total amount of your library. Also they might hide adapter dimer contamination. But that should be obvious after denaturation and running on an RNA chip.

        --
        Phillip

        Comment

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