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
            New Genomics Tools and Methods Shared at AGBT 2025
            by seqadmin


            This year’s Advances in Genome Biology and Technology (AGBT) General Meeting commemorated the 25th anniversary of the event at its original venue on Marco Island, Florida. While this year’s event didn’t include high-profile musical performances, the industry announcements and cutting-edge research still drew the attention of leading scientists.

            The Headliner
            The biggest announcement was Roche stepping back into the sequencing platform market. In the years since...
            03-03-2025, 01:39 PM
          • seqadmin
            Investigating the Gut Microbiome Through Diet and Spatial Biology
            by seqadmin




            The human gut contains trillions of microorganisms that impact digestion, immune functions, and overall health1. Despite major breakthroughs, we’re only beginning to understand the full extent of the microbiome’s influence on health and disease. Advances in next-generation sequencing and spatial biology have opened new windows into this complex environment, yet many questions remain. This article highlights two recent studies exploring how diet influences microbial...
            02-24-2025, 06:31 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by seqadmin, 03-03-2025, 01:15 PM
          0 responses
          180 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 02-28-2025, 12:58 PM
          0 responses
          275 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 02-24-2025, 02:48 PM
          0 responses
          663 views
          0 likes
          Last Post seqadmin  
          Started by seqadmin, 02-21-2025, 02:46 PM
          0 responses
          268 views
          0 likes
          Last Post seqadmin  
          Working...
          X