Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • suryasaha
    Member
    • Mar 2011
    • 27

    #1

    IMAGE2 input and parameters

    I am able to run IMAGE2 after creating read.placed.original and contigs.fa.original in the required format. Here are my questions:
    * Is it possible to supply multiple insert libraries to IMAGE? If yes, how?
    * What is the difference between "insert size" and "velvet ins_len" in submit.iteration_.log?
    * I am working with a bacterial genome. So I assume that all contigs will go into Supercontig1 in read.placed.original. Is that correct?

    Please let me know if any question is unclear. Is there a IMAGE mailing list? I was not able to find one on the sourceforge project page. Thanks

    -Surya
  • suryasaha
    Member
    • Mar 2011
    • 27

    #2
    Here is what I learned from the authors
    * Is it possible to supply multiple insert libraries to IMAGE? If yes, how?
    No
    * What is the difference between "insert size" and "velvet ins_len" in submit.iteration_.log?
    insert size is the mapping parameter used in ssaha or bwa. velvet ins_len is the insert size used in velvet.
    * I am working with a bacterial genome. So I assume that all contigs will go into Supercontig1 in read.placed.original. Is that correct?
    Yes

    -Surya

    Comment

    • dolphing
      Junior Member
      • Dec 2010
      • 3

      #3
      good job~thx

      Comment

      • maasha
        Senior Member
        • Apr 2009
        • 153

        #4
        I am looking for some more info on "insert size" and "velvet ins_len". It is not clear which is used for what?

        My additional Illumina data have a insert size of 260.

        I can set "velvet ins_len" as a parameter to 000_walk_all_raw.pl, but where is "insert size" set?

        (IMAGE2 would benefit from a bit more documentation).


        Cheers


        Martin

        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, Yesterday, 11:13 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, Yesterday, 10:48 AM
        0 responses
        17 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        35 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        42 views
        0 reactions
        Last Post SEQadmin2  
        Working...