Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • adapter dimer

    Hi everyone,

    I am having issues with adapter dimer in my RNA preps for sequencing. I have read about the dimer eliminator but it is expensive. Is there another method to deal with this or is there a kit that does better? I have read about the netflex small RNA kit (BIOO scientific), however, is there something I can do without buying some other kit or LNA?

  • #2
    If you provide specific information such as the kit used for library prep, the issues that you see and measures taken o alleviate it that has not worked well, you are more likely to get useful responses. There are many methods and kits for RNA library prep and general advice might not be helpful for your adapter-dimer issues.

    Comment


    • #3
      We are using the small RNA library kit from NEB. We are doing PAR-CLIP ad then adapting the RNA for illumina sequencing. After PCR amplification, we see a lot of adapter dimer in our PCR samples. In fact, it pver-rides the samples. I have read about dimer eliminator but was wondering if there is a simpler way to avoid this adapter dimer product or even reduce it. I think also that increasing the starting RNA sample amount might be easier but if anyone has done PAR-CLIP before, the resulting RNA is very low.

      Comment


      • #4
        Dimer eliminator will not help to reduce adapter-dimmer formation when using NEB small RNA kit. Annealing of RT primer (after 3’ adapter ligation) to un-ligated 3’ adapter would effectively reduce primer-dimer formation by transforming 3’ adapter in to a double-stranded DNA that is not a substrate for T4 RNA ligase used for 5’ adapter ligation. I wonder what your RNA size range is and if you have any RNA and prepped library Bioanalyser trace. Primer-dimer that you observe might have different origin (it is less likely product of ligations between 3’ and 5’ adapters) and that can be identified by examining primer-dimer sequences. Cutting library fragments with expected size from gel is one way to reduce primer-dimer reads in sequencing data. It might also be possible to reduce them by modifying library prep protocol.

        Comment

        Latest Articles

        Collapse

        • seqadmin
          Latest Developments in Precision Medicine
          by seqadmin



          Technological advances have led to drastic improvements in the field of precision medicine, enabling more personalized approaches to treatment. This article explores four leading groups that are overcoming many of the challenges of genomic profiling and precision medicine through their innovative platforms and technologies.

          Somatic Genomics
          “We have such a tremendous amount of genetic diversity that exists within each of us, and not just between us as individuals,”...
          05-24-2024, 01:16 PM
        • seqadmin
          Recent Advances in Sequencing Analysis Tools
          by seqadmin


          The sequencing world is rapidly changing due to declining costs, enhanced accuracies, and the advent of newer, cutting-edge instruments. Equally important to these developments are improvements in sequencing analysis, a process that converts vast amounts of raw data into a comprehensible and meaningful form. This complex task requires expertise and the right analysis tools. In this article, we highlight the progress and innovation in sequencing analysis by reviewing several of the...
          05-06-2024, 07:48 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, 06-03-2024, 06:55 AM
        0 responses
        12 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 05-30-2024, 03:16 PM
        0 responses
        24 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 05-29-2024, 01:32 PM
        0 responses
        29 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 05-24-2024, 07:15 AM
        0 responses
        215 views
        0 likes
        Last Post seqadmin  
        Working...
        X