Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • hclee
    Junior Member
    • Jul 2011
    • 1

    #1

    Mapping very short (<20 bp) reads

    Hi,

    I've been a SOAP2 user but recently got some very short reads (<20 bp) to map to a reference genome. Can someone please suggest an aligner which can handle the problem? SOAP seems to map only reads >30 bp.

    Thank you.
  • Kennels
    Senior Member
    • Feb 2011
    • 149

    #2
    Originally posted by hclee View Post
    Hi,

    I've been a SOAP2 user but recently got some very short reads (<20 bp) to map to a reference genome. Can someone please suggest an aligner which can handle the problem? SOAP seems to map only reads >30 bp.

    Thank you.
    You could try bowtie or bwa

    Comment

    • sdarko
      Member
      • Apr 2009
      • 52

      #3
      Command-line BLAST could work well.

      Comment

      • husamia
        Member
        • Apr 2010
        • 66

        #4
        I am curious about your data and brings unrelated question? Aren't <20bp reads considered ambigous? Technically its possible that good amount of your reads align to multiple regions in genome. Hence (ambiguous). Is there data to support what is a good enough read length that provides least amount of ambiguous-ness?
        I was playing around with searching and as long as I enter random sequence shorter than 20bps in general I get multiple perfect match with genome.
        Last edited by husamia; 07-15-2011, 08:51 AM.

        Comment

        • mnkyboy
          Member
          • Mar 2009
          • 87

          #5
          Originally posted by husamia View Post
          I am curious about your data and brings unrelated question? Aren't <20bp reads considered ambigous? Technically its possible that good amount of your reads align to multiple regions in genome. Hence (ambiguous). Is there data to support what is a good enough read length that provides least amount of ambiguous-ness?
          I was playing around with searching and as long as I enter random sequence shorter than 20bps in general I get multiple perfect match with genome.
          I was wondering about this too. Shorter than 20 you cannot differentiate them from random sequences.

          Comment

          Latest Articles

          Collapse

          • 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
          • SEQadmin2
            New Genomics Technologies Take Aim at Long-Standing Limits
            by SEQadmin2


            Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

            We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
            ...
            09-28-2026, 10:25 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 10-15-2026, 10:52 AM
          0 responses
          26 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-14-2026, 05:39 AM
          0 responses
          32 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-13-2026, 09:56 AM
          0 responses
          31 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-09-2026, 11:14 AM
          0 responses
          28 views
          0 reactions
          Last Post SEQadmin2  
          Working...