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  • kainsteven
    Member
    • Jul 2009
    • 16

    #1

    Hello from NuGEN Technologies

    Steve Kain here. We have recently introduced a solution for RNA-Seq sample prep with inputs of total RNA in the range of 500 pg to 100 ng. The product is double-stranded cDNA in the size range of 50-1,500 bases. I look forward to monitoring this site to learn more about NGS sample prep needs, and progress in the field in general. We are located in the SF Bay Area.

    Cheers,
    Steve
  • tanals
    Junior Member
    • Oct 2009
    • 3

    #2
    Compatibility with SOLiD?

    Hi Steve,
    Is the Ovation RNA-Seq kit compatible with the SOLiD sequencers? We are working with pg quantities of RNA at the moment and will be lucky to get 1ng at the end and want to screen for miRNAs.
    Cheers

    Comment

    • kainsteven
      Member
      • Jul 2009
      • 16

      #3
      Yes, compatible with SOLiD and 454

      The product from the Ovation RNA-Seq workflow is ds cDNA, and hence compatible with any library prep system using this starting material. We have several customers that have used the system successfully on SOLiD.

      Best,
      Steve

      Comment

      • acpatel
        Junior Member
        • Jun 2009
        • 5

        #4
        specific question

        Steve,

        Could Prelude be used with OCT-embedded tissue samples (very tiny tissue samples)? For OCT-embedded frozen samples, would one use:
        Ovation® RNA-Seq FFPE System
        Ovation® RNA-Seq
        Ovation® 3'-DGE System

        We want have 24 paired samples (12 pairs), and would like to get gene expression data from these samples. Using Qiagen's micro kit, we have RINs and yields ranging from 2.3-5.9 RIN, 9.1 to 2140 mass (ng).

        Thanks,
        Anand

        Comment

        • kainsteven
          Member
          • Jul 2009
          • 16

          #5
          Hi Anand,

          Can you please provide some details regarding the impact of OCT treatment on the samples? Ovation RNA-Seq FFPE is preferable if you have degraded samples, and/or cross-linking typically brought about by formalin fixation.

          Best,
          Steve

          Comment

          • josdegraaf
            Member
            • Mar 2010
            • 33

            #6
            Hi,

            What is different from the 'normal' rna-seq kit to the FFPE ?

            Thanks

            Comment

            • josdegraaf
              Member
              • Mar 2010
              • 33

              #7
              I forgot, is there anyone in here that used the FFPE kit with succes?

              thanks

              Comment

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