Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cascoamarillo
    Senior Member
    • Oct 2010
    • 164

    #1

    Weird library with ScriptSeq

    Hi,

    I'm wondering if anyone else has obtained a result like this in a library construction. Also, a target of this post is the Epicentre tech assist.

    I've been contructing a library with ScripSeq Library Preparation kit (Illumina-compatible) from Epicentre. The starting material was rRNA depleted (from Trizol total RNA extraction). The initial RNA and rRNA depleted sample looks good in the bioanalyzer. But after following the protocol and purify the library with XP beads (I also tried MinElute columns, with same result but a lot of primer-dimers), the library pattern does not look good. Attached is the bioanalizer trace from one of the samples (with 15 cycles in the PCR amplification step, having already used between 10-15).

    Thanks
    Attached Files
  • Olaf Blue
    Member
    • Nov 2010
    • 58

    #2
    Hello-

    Can you tell me which product was used to perform rRNA removal, and which ScriptSeq Kit was used to generate the library? Was the original total RNA treated with DNAse I after the trizol extraction? Just some basic questions to gather information to help with finding any issues.

    Comment

    • cascoamarillo
      Senior Member
      • Oct 2010
      • 164

      #3
      Sure!

      I use The RiboMinus™ Eukaryote Kit for RNA-Seq (Invitrogen) to perform the rRNA removal. I work with a fungi, and I've also try The Ribo-Zero™ rRNA Removal Kits (Human/Mouse/Rat) non-magnetic; but with poor rRNA remove.

      The kit is The ScriptSeq™ mRNA-Seq Library Preparation Kit (Illumina®-compatible), the version 1.

      And no, the original RNA was not treated with DNaseI (it's considered for the future).

      Thanks

      Comment

      • Olaf Blue
        Member
        • Nov 2010
        • 58

        #4
        Hi, thanks for the reply! I'd definitely recommend a DNAse I treatment of your RNA - we've recommended that in the past and it has definitely helped improve the library as it is possible that the cDNA synthesis primer can bind to residual DNA and get extended and thus create a segment of your library.

        Rather than using Ribo-Minus or Ribo-Zero, have you thought about using poly-A capture to remove non-mRNA species from the sample? Given the difficulty with the Ribo-Zero and Ribo-Minus Kits with the samples, the mRNA capture might be a better solution.

        Just some thoughts.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM
        • SEQadmin2
          Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
          by SEQadmin2



          Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
          ...
          07-09-2026, 11:10 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 07-31-2026, 02:55 AM
        0 responses
        19 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-24-2026, 12:17 PM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-23-2026, 11:41 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 07-20-2026, 11:10 AM
        0 responses
        26 views
        0 reactions
        Last Post SEQadmin2  
        Working...