Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • christophpale
    Member
    • May 2010
    • 16

    #1

    No further enrichment after the 2nd Truseq exome capture

    Hi,
    We have just started to make our own TruSeq libraries and do the Truseq multiplex exome capture. We found that the second enrichment did not have any effect on the input (i.e. the amount we put in was the amount we got out after the second enrichment reaction).
    Can some one please comment on their experience with TruSeq exome capture.
    1. If you put in 500ng (x 6 samples = 300ng) of the pooled TruSeq library for Truseq multiplex exome capture, what is the yield after the first capture?
    2. What is the yield after the second capture?
    3. How much of the capture material do you need for sequencing on a hiseq?
    thanks
    Christoph
  • sehrrot
    Member
    • Jul 2010
    • 58

    #2
    Hi Chris

    I haven't measured the yield after the first capture. But the 2nd capture's yield before amplification was around 13ng/ul in 10 ul and then after amplification the yield was 5 ng/ul in 30 ul (higher concentration on pre-amplification may be due to some un-cleaned beads in samples?). This is a singlet capture.

    Comment

    • Maqbool
      Junior Member
      • Nov 2011
      • 2

      #3
      Hi Sehrrot,

      We get the same amount of captured library as you have written, 4-5 ng/ul in 30 ul.

      What is your experience for cluster density adjustment? I need to load 3-4 times more than a regular genomic library. I would also like to know your experience with data analysis regarding the PCR duplicates and the fold coverage depth.

      Comment

      • ageneheo
        Junior Member
        • Sep 2012
        • 4

        #4
        Sehrrot,

        It is hard to understand the yield of exome capture library before PCR and after PCR.

        Did you find any answer about that?

        Comment

        Latest Articles

        Collapse

        • 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
        • SEQadmin2
          New Genomics Technologies Take Aim at Long-Standing Limits
          by SEQadmin2


          Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

          We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
          ...
          09-28-2026, 10:25 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 10-22-2026, 11:13 AM
        0 responses
        35 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        25 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        41 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        45 views
        0 reactions
        Last Post SEQadmin2  
        Working...