Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • wiart
    Junior Member
    • Feb 2008
    • 1

    #1

    Newbler de novo assembly and repeats

    Hi,

    I'm using Newbler de novo assembler from the command line (runAssembly), with a set of 18,000 reads.
    I'd like to tweak the "repeat" threshold since Newbler estimate that >98% of the reads are repeats, and I end up with 0 contigs...

    Here is the command:
    runAssembly -ss 12 -sl 16 -sc 1 -ml 25 -mi 80 -o ./newbler seqs.fa

    BTW, do somebody have information about how this "repeat detection" step work? I couldn't find much about that in the GS manual... (the manual mention a -rst repeat score threshold, but only for assembly to a reference, with runMapping command)

    Thanks,
    Laurent
    Last edited by wiart; 07-24-2009, 11:33 AM. Reason: added information
  • jnfass
    Member
    • Aug 2008
    • 88

    #2
    Just a few thoughts (no direct answers) ...

    I'm sorry - I can't help you with tweaking the assembly parameters (such as -rst) as I've never used anything but the defaults ...
    But, have you looked at your sequences? Maybe newbler's right ...

    I often look for unusually frequent sequences in a quick and dirty way -- something like:
    cat seqs.fa | grep -v ">" | cut -c1-25 | sort | uniq -c | sort -rn -k1,1
    But that'll only tell you if there you have contamination at the beginnings (or in the same positions, if you cut other characters) in every read (of course you miss the ones on the other strand).
    More specifically to repeats - have you tried blasting to a repeat library?

    Comment

    • alex_dl
      Junior Member
      • Mar 2009
      • 2

      #3
      I found the same kind of behavior in reads with vector sequence.
      Be sure that you provide a trimming sequence if the library was constructed with a vector (as in a fosmid library)

      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
      23 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      27 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-13-2026, 09:56 AM
      0 responses
      24 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...