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  • rjoyons
    Junior Member
    • Jul 2013
    • 4

    Will a low 260/230 ratio effect results using MiSeq?

    Hi Guys!

    I am new to Illumina sequencing and I have a sample pretty much ready to go containing around 1ug of genomic DNA. I checked the quantity using agarose gel comparing the genomic band to a quantitative ladder and another quantitative marker. The 260/280 ratio is 1.8 but the 260/230 ratio is only 1.2

    Will this be detrimental to a run with a MiSeq?

    Thanks in advance!
  • microgirl123
    Senior Member
    • Jun 2012
    • 199

    #2
    If I was prepping your library, I would strongly urge you to clean it up more before submitting it. We've made a couple libraries with poor 260/230 ratios (<1.5) and gotten yields too low to load on the MiSeq.

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