Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • huma Asif
    Member
    • Oct 2010
    • 53

    #1

    Denovo assembly problem

    I am a new on this platform and need to seek help with some queries
    I am sequencing two bacterial genomes but the problem i am having is with its assembly for one of the genome i got scaffold N50 70234 and for other scaffold N50 is 3000.I have assembled these genome using SOAP denovo .I need to seek ur help in knowing is this N50 good for denovo assembly
    what else i can do to improve scaffold N50 of these genomes
    Regards
  • Cofactor Genomics
    Registered Vendor
    • Jan 2010
    • 52

    #2
    Were you expecting more similar N50s because the organisms were very similar?
    Were the two projects sequenced to the same depth using the same library type and read configuration? How about the isolation, were both from a clean/clonal isolation?

    In order for our team to make large strides in N50, we had to get very critical on sample purity, we integrated additional custom library types, and third we used both short read and long read platforms.

    Jarret Glasscock
    Cofactor Genomics

    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, 10-22-2026, 11:13 AM
    0 responses
    36 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-22-2026, 10:48 AM
    0 responses
    28 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-15-2026, 10:52 AM
    0 responses
    41 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-14-2026, 05:39 AM
    0 responses
    45 views
    0 reactions
    Last Post SEQadmin2  
    Working...