Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • chariko
    Member
    • Jun 2010
    • 56

    #1

    MIRA de novo assembly with reference genome doubt

    Hello everybody,

    I recently downloaded Mira software and I am getting some doubts I hope someone can help me to resolve.

    My experiment consists in a paired end Illumina de novo assembly having a similar reference genome. As explained in the Mira Manual, it is recommended to do first a mapping and afterwards when the mapping has ended, get the list with the not mapped reads and do a de novo assembly with them (taking them from the original fastq file).

    As result I got 2 caf files, one with the results of the mapping and other one witih the results with the de novo assembly.

    When loading this data to gap5 (first mapped reads and then importing the de novo caf results) it does not recognize the pairs comming from diferent files. I wonder if it is possible to join the 2 caf files before loading the data to gap5. I hope this will turn in pairs to be recognized.

    Any other suggestion on how to proceed will be appreciated.

    Thanks in advance,
  • sklages
    Senior Member
    • May 2008
    • 628

    #2
    You might want to ask this on the mira mailing list. It is likely that you obtain more help and/or solutions there ..

    Comment

    • chariko
      Member
      • Jun 2010
      • 56

      #3
      You are right, I got there the answer. Anyway the answer on how to join the caf files was as easy as:

      cat file1.caf file2.caf >combined.caf

      Comment

      • sklages
        Senior Member
        • May 2008
        • 628

        #4
        Maybe you should leave a pointer here to the mailing list answer for people to see what the solution of your problem was.

        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
          ...
          Yesterday, 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, 05:39 AM
        0 responses
        11 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-13-2026, 09:56 AM
        0 responses
        14 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-09-2026, 11:14 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 09-29-2026, 09:51 AM
        0 responses
        77 views
        0 reactions
        Last Post SEQadmin2  
        Working...