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  • mzpitman
    Junior Member
    • May 2011
    • 7

    hello from Mark at Omixon

    Hi All-

    I work at Omixon, developers of the most accurate NGS mapping, alignment, and variant calling toolkit available. More at www.omixon.com.

    Our mission is simple - make NGS clinically relevant. Further to this we see that much higher accuracy is necessary for NGS analysis.

    We are actively seeking testers for our toolkit. Please go to our site and register for the toolkit. It's free to play with through the year's end. We very much want to have your feedback on the experience you've had with our tools so please if you download and try it out let us know how it went!

    Cheers,
    Mark

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  • GATTACAT
    Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by GATTACAT
    Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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  • SEQadmin2
    Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by SEQadmin2


    I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

    Here are nine questions we think about, in roughly the order they matter, before...
    06-18-2026, 07:11 AM

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