Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • arrchi
    Member
    • Mar 2011
    • 46

    #1

    questions of illumina pe reads fastqc results

    We have a set of illumina paired-end RNA seq 50 bp data. The plot of per base sequnece quality is fine (I think), but the plot of Kmer Content looks very weird. I want to have some suggestions about what is wrong in this data. Does it suggest there is an adaptor contamination? Will trimming adaptors help? How should I find the sequence of these adaptors?

    Thanks a lot.
    Attached Files
  • mattanswers
    Member
    • Oct 2009
    • 65

    #2
    The pink peak is CGTCT and the red is GTCTG, so I would guess you have the sequence CGTCTG in positions 15-20. Likewise, the it seems like the sequence, TATCTCGTATG in positions 38-48.

    Somewhere on the SeqAnswers site has been posted Illumina paired end adaptors.

    I found CGTCT in a few 5' Illumina adaptors, however, the CGTCT in the adaptors is always followed by a T and not a G.

    Also, TCTCG is found in a couple of 3' Illumina adaptors, but it is followed by AGCATAC. So, I am not sure as to what the peaks you have are showing, and the adaptor sequences I have come from 2008.

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
      by SEQadmin2




      NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
      Today, 06:46 AM
    • 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

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, 10-28-2026, 09:57 AM
    0 responses
    22 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-28-2026, 09:51 AM
    0 responses
    14 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 11:13 AM
    0 responses
    67 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    47 views
    0 reactions
    Last Post SEQadmin2  
    Working...