Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dummyseq
    Member
    • Nov 2012
    • 13

    #1

    Nextera Exome Enrichment kit

    Hi,Hello,

    I am using 150ng FFPE DNA to prepare a library for HiSeq. After 1st amplification, DNA concentrations are too low, not enough for 500ng suggested for hybridisation. Followed the protocol excatly.

    Any advise appreciated. Should I increase PCr cycles from 10 to 12 ?? But with Sure Select Agilent kits we haev seen that increasing PCr cycles decreases conc of DNA.

    Thanks
  • epistatic
    Senior Member
    • Mar 2009
    • 129

    #2
    How well did the tagmentation work with FFPE samples? You may have many fragments with one integration site, not allowing for the majority of your sample to have both adapters for the PCR step.

    When I have used nextera in the past with amplicons I had to pad the ends to allow for integration space and still sequence the region of interest. I have processed 48 samples with cell line DNA with nextera exome and a bit skeptical it would work well with FFPE.

    For FFPE exome I prefer a standard library followed by capture. I usually don't have to shear the DNA very much if at all before making a library.

    Comment

    • dummyseq
      Member
      • Nov 2012
      • 13

      #3
      How exactly did you pad the ends??

      Thanks

      Comment

      • epistatic
        Senior Member
        • Mar 2009
        • 129

        #4
        Apologies for the unclear terminology. I should have said I made the amplicon larger. If I just used the standard amplicon nextera would integrate often only once or if twice it would cut off parts that I wanted to sequence. Too small of amplicons didn't work at all with nextera.

        Comment

        • snetmcom
          Senior Member
          • Oct 2008
          • 159

          #5
          I would agree that Nextera with FFPE is not a good fit. You may see a reduced on target as well. Traditional library methods will likely yield better results as epistatic stated.

          Comment

          • dummyseq
            Member
            • Nov 2012
            • 13

            #6
            Has anyone tried increasing TDE for more than 150ng DNA input? We are getting low values even after increasing input DNA and PCr cycles to 12

            Any input with FFPE DNA Nextera protocol will be helpful

            THanks

            Comment

            • ymc
              Senior Member
              • Mar 2010
              • 496

              #7
              Has this kit been renamed to "Nextera Rapid Capture Exome and Expanded Exome Kits"?

              Comment

              • dummyseq
                Member
                • Nov 2012
                • 13

                #8
                None of the above. It just says "Nextera Exome Enrichment " Kit divided into 3 boxes,all labelled the same

                Comment

                • dgasx8
                  Junior Member
                  • Jul 2013
                  • 2

                  #9
                  Originally posted by dummyseq View Post
                  Has anyone tried increasing TDE for more than 150ng DNA input? We are getting low values even after increasing input DNA and PCr cycles to 12

                  Any input with FFPE DNA Nextera protocol will be helpful

                  THanks
                  Hi dummyseq,
                  what about your libraries from FFPE samples? Did you obtain and captured whole exome libraries good for Hiseq?

                  Comment

                  Latest Articles

                  Collapse

                  • SEQadmin2
                    16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
                    by SEQadmin2




                    NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
                    Today, 06:46 AM
                  • SEQadmin2
                    Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                    by SEQadmin2



                    Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                    Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                    ...
                    10-14-2026, 09:55 AM

                  ad_right_rmr

                  Collapse

                  News

                  Collapse

                  Topics Statistics Last Post
                  Started by SEQadmin2, 10-28-2026, 09:57 AM
                  0 responses
                  23 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-28-2026, 09:51 AM
                  0 responses
                  15 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-22-2026, 11:13 AM
                  0 responses
                  68 views
                  0 reactions
                  Last Post SEQadmin2  
                  Started by SEQadmin2, 10-22-2026, 10:48 AM
                  0 responses
                  48 views
                  0 reactions
                  Last Post SEQadmin2  
                  Working...