Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • liaojinyue
    Junior Member
    • Oct 2012
    • 8

    #1

    Big variation of output for individual library

    Hello all,

    We recently received our RNA-seq data from the vendor. We sequenced 8 libraries as a pool and we were supposed to get around 30M reads for each sample. After reviewing the data, we saw uneven read number for the samples ranging from around 13M to 43M. According to the vendor, they did perform q-PCR to quantify the libraries and the explanation was that the libraries behave differently when pooled together.

    So how accurately can we control the read distribution among libraries in the pool? Is it normal to see variation this big? Really appreciate if anyone can share experience.

    Jason
  • sara_ahmed
    Member
    • Nov 2011
    • 13

    #2
    It is normal to see some variability even if libraries are pooled and quantified by qPCR. That said, what you describe seems like a much larger variability than normal especially if all the libraries pooled together were generated with a similar library protocol. You tend to see more variability when mixing different library types together (small RNA libs with mRNA libs for example) because they tend to cluster differently. I would say its normal to see about 20% difference between different samples in a pool if the libraries are made the same way and quantified by qPCR.

    Sara Ahmed, PhD | Director of Sequencing | Cofactor Genomics
    4044 Clayton Ave | St. Louis, MO 63110 | tel. (314) 531-4647

    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
    36 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    28 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...