Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • New k-mers overpresentation by adapter trimming

    Hi
    I am working on an Illumina Hiseq paired end whole genome data.

    The data shows overrepresentation of adapter sequences such as TruSeq Adapter, Index 14 (97% over 40bp) according to the quality reported by the fastqc analysis.

    So I performed trimming of the reads by the TruSeq-PE adapter sequences in trimmomatic data and performed fastqc after trimming.

    The post-trimming data shows appearance of new k-mers overrepresented at various positions within 0-50 bp. The bbmap analysis for the percentage match still shows no remarkable mismatch problems, indicating that the k-mers could be genomic.

    I have attached the before and after trimming k-mer overpresentation plots herewith.

    This observation makes me doubt the need of trimming in paired end data.

    My question is :
    Do we indeed need to perform trimming in such cases ?
    Any suggestion on change in the trimming was needed such as using only the overrepresented adapter sequences and but not other adapters from the same library in the analysis.

    Thanks
    Attached Files
    Last edited by ty23991; 06-22-2015, 11:28 AM.

  • #2
    Considering the Y-axis is log-scale, it looks like trimming vastly reduced the rate of overrepresented kmers (though I've never been sure exactly how to interpret the graph), which would be a good thing. What kind of trim rate did you get?

    Also, note that if you have contamination by synthetic artifacts of set length, that will not affect BBMap's error rate histograms because the fully-artifact reads won't map to your reference.

    Comment


    • #3
      Hi Brian
      Thanks for the suggestion.

      Here is the trimming report:

      Trimming was performed by using 1 prefix pairs, 10 forward/reverse sequences

      Input Read Pairs: 532073495
      Both Surviving: 510614940 (~96 %)
      Forward Only Surviving: 13002991 (2.4%)
      Reverse Only Surviving: 3487288 (0.7%)
      Dropped: 4968275 (0.9%)

      Comment


      • #4
        It's hard to extrapolate from that to derive the number of reads/bases that were trimmed due to adapter sequence, but it looks like trimming was probably a good idea in that case.

        Comment


        • #5
          Thanks for the idea. I am thinking to perform the alignment on both with and without trimming and compare the results.

          Comment

          Latest Articles

          Collapse

          • seqadmin
            Addressing Off-Target Effects in CRISPR Technologies
            by seqadmin






            The first FDA-approved CRISPR-based therapy marked the transition of therapeutic gene editing from a dream to reality1. CRISPR technologies have streamlined gene editing, and CRISPR screens have become an important approach for identifying genes involved in disease processes2. This technique introduces targeted mutations across numerous genes, enabling large-scale identification of gene functions, interactions, and pathways3. Identifying the full range...
            08-27-2024, 04:44 AM
          • seqadmin
            Selecting and Optimizing mRNA Library Preparations
            by seqadmin



            Sequencing mRNA provides a snapshot of cellular activity, allowing researchers to study the dynamics of cellular processes, compare gene expression across different tissue types, and gain insights into the mechanisms of complex diseases. “mRNA’s central role in the dogma of molecular biology makes it a logical and relevant focus for transcriptomic studies,” stated Sebastian Aguilar Pierlé, Ph.D., Application Development Lead at Inorevia. “One of the major hurdles for...
            08-07-2024, 12:11 PM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 08-27-2024, 04:40 AM
          0 responses
          16 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 08-22-2024, 05:00 AM
          0 responses
          293 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 08-21-2024, 10:49 AM
          0 responses
          135 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 08-19-2024, 05:12 AM
          0 responses
          124 views
          0 likes
          Last Post seqadmin  
          Working...
          X