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  • Genohub
    Registered Vendor
    • Mar 2013
    • 210

    Next Gen Sequencing Marketplace

    I’m pleased to announce the opening of Genohub to researchers. Genohub is a new online service designed for those interested in ordering next gen sequencing services. Our goal is to help you easily find and order the right sequencing solutions for your research projects.

    We are constantly working with a growing number of reputable NGS providers who use Genohub to list up-to-date information on their regular services as well as their excess sequencing capacity. This enables you to have easy access to accurate, detailed, and current sequencing and library preparation services from a variety of service providers. These services are intelligently packaged and priced by our software to match your project requirements.

    With all of this information at your disposal you can easily select the right solution and submit your project. Throughout the process our science staff is available to answer your questions and help you identify sequencing solutions that are best suited to your specific needs.

    Shop, order, track and receive NGS results with guaranteed turnaround times. Give it a try by searching for NGS services today.
  • LOH
    Registered Vendor
    • Jul 2010
    • 23

    #2
    Can you list our company as a NGS provider in Genohub?

    Quick Biology is committed to provide the best value to our customers. We are equipped with one HiSeq 4000, two NextSeq500, one MiSeq and one Ion Proton. Our illumina HiSeq 4000 runs twice a week on a routine basis. For each project we provide: (1) Fast turn around time (10-20 business days); (2) Very competitive price for RNA-Seq and Whole Exome Seq; (3) Advanced bioinformatic analysis, including analysis for RNA splicing/RNA editing.

    Comment

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    • GATTACAT
      Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
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      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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