Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dawe
    Senior Member
    • Apr 2009
    • 258

    #1

    Forward strand bias?

    Hi all,
    this may be something known... anyway, tags coming from Illumina sequencing method (GA II here) seem to map preferentially on forward strand... I haven't check if there is a statistically significant variation, but apparently tags aligned on forward strand are 2-5% more (in various ChIP-seq and also in genome resequencing).
    I wonder which could be the source of this variation... The library prep? The cluster generation? The aligner? None of these steps makes sense to me...

    d
  • steven
    Senior Member
    • Aug 2009
    • 269

    #2
    ?! strange indeed!
    statistical significance may be an important point here.. is the bias constant across chromosomes?
    s.

    Comment

    • bioinfosm
      Senior Member
      • Jan 2008
      • 483

      #3
      What aligner are you using? Probably you could use a different one and see what happens to the bias
      --
      bioinfosm

      Comment

      • maubp
        Peter (Biopython etc)
        • Jul 2009
        • 1544

        #4
        I'd also suggest taking your references and reverse complementing them. Then repeat the alignment on the RC reference and see what happens. If this is just a software artefact, then you should see more reads on the new forward strand (i.e. what was the reverse strand in the original reference).

        Comment

        • steven
          Senior Member
          • Aug 2009
          • 269

          #5
          My bet would be a single genomic position (on the forward strand) that gets a gazillion of copies of a single read (generated by a contaminant, an amplification artifact, an incorrect filter, or something else).

          Comment

          • steven
            Senior Member
            • Aug 2009
            • 269

            #6
            Originally posted by dawe View Post
            Hi all,
            this may be something known... anyway, tags coming from Illumina sequencing method (GA II here) seem to map preferentially on forward strand... I haven't check if there is a statistically significant variation, but apparently tags aligned on forward strand are 2-5% more (in various ChIP-seq and also in genome resequencing).
            I wonder which could be the source of this variation... The library prep? The cluster generation? The aligner? None of these steps makes sense to me...

            d
            Hi,
            any news regarding this issue?
            thanks,
            s.

            Comment

            • dawe
              Senior Member
              • Apr 2009
              • 258

              #7
              Originally posted by steven View Post
              Hi,
              any news regarding this issue?
              thanks,
              s.
              Not yet... I've been busy on other issue but I will investigate this further...

              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...
                Yesterday, 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
              25 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-28-2026, 09:51 AM
              0 responses
              16 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 11:13 AM
              0 responses
              71 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-22-2026, 10:48 AM
              0 responses
              48 views
              0 reactions
              Last Post SEQadmin2  
              Working...