Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • meriem
    Member
    • May 2016
    • 19

    #1

    can I remove the N's in my sequence?

    Hello,

    I'm having a problem with mine assembly, I have a bacterial genome of 3.7bp assembled into 24 contigs, which was part of an under submission research, the reviewer gave me as a feedback that I should have a gap free sequence; Unfrontutly I can't not re-do the sequencing or use Pacbio. so I used ragout for reference-assisted assembly to improve the quality of my assembly; I got 1 scaffold of 3.7 bp, but a lot of ns (40000 n), how can I fix this problem? is this software reliable since I got some small fragment left? can I remove the ns without affecting the sequence?

    thank you
  • cstack
    Member
    • May 2017
    • 16

    #2
    Just so we are using the same terminology: An assembly gap is typically represented by a series of N's connecting two contigs; the product of 2+ contigs connected by gaps is referred to as a scaffold.

    Your 24 original contigs contained no gaps (Ns), correct? I would confirm this first

    I have never used Ragout, but it seems to order and connect contigs based on a reference genome; in the process of connecting contigs, gap characters (Ns) are added. There is nothing atypical about this -- Without looking over your manuscript, it is difficult to say why the review took issue with the gaps.

    Anyhow, you can use
    Code:
    seqtk cutN -n 1 ragout.fasta
    to break up the single, 3.7(M?)bp scaffold produced by ragout into a set of gap-free contigs.

    Comment

    • meriem
      Member
      • May 2016
      • 19

      #3
      Originally posted by cstack View Post
      Just so we are using the same terminology: An assembly gap is typically represented by a series of N's connecting two contigs; the product of 2+ contigs connected by gaps is referred to as a scaffold.

      Your 24 original contigs contained no gaps (Ns), correct? I would confirm this first

      I have never used Ragout, but it seems to order and connect contigs based on a reference genome; in the process of connecting contigs, gap characters (Ns) are added. There is nothing atypical about this -- Without looking over your manuscript, it is difficult to say why the review took issue with the gaps.

      Anyhow, you can use
      Code:
      seqtk cutN -n 1 ragout.fasta
      to break up the single, 3.7(M?)bp scaffold produced by ragout into a set of gap-free contigs.
      Thank you for your reply,
      My 24 contigs doesn't contain any N's.
      Im' doing a comparative genomic analysis of 2 strains from an extrem envirenement, I got this msg from the reviewer " In that the strains on which this Genome Report is based can be grown in culture, it is necessary to produce gap-free sequences for both strains, since the data would be more generally useful for the community at large. Given the high coverage that is already available, it would probably be necessary to take a more direct approach (rather than increasing coverage)."

      If I Use this commande I will go back to my initial contigs, No?

      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
      29 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-13-2026, 09:56 AM
      0 responses
      25 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...