Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • santhosh003
    Junior Member
    • Nov 2009
    • 3

    #1

    Assembling Sanger Reads

    Hi,

    I am new to genomics. I have got sanger reads. They are in .ab1, phd.1, seq,,scf format.
    How can I do reference assembly of these files. Is there any software or program to convert all these files into a single fastq file? or is there any assembler to take all these files as input and do the assembly? What could be the process of doing reference assembly for these reads. Any help is appreciated. Thank you so much.
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    For Sanger reads, you could try PHRED/PHRAD/consed

    Comment

    • sklages
      Senior Member
      • May 2008
      • 628

      #3
      or MIRA3
      Download MIRA for free. MIRA V5 is available only on GitHub! The V4 version released here on SourceForge stay up as some automated release fetching packages rely on V4.


      both run fine in our hands .. :-)

      cheers,
      Sven

      Comment

      • skycreative
        Member
        • Jan 2010
        • 33

        #4
        Originally posted by maubp View Post
        For Sanger reads, you could try PHRED/PHRAD/consed
        http://www.phrap.org/phredphrapconsed.html
        agree with you , it is very effective

        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
        28 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        20 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-15-2026, 10:52 AM
        0 responses
        38 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-14-2026, 05:39 AM
        0 responses
        44 views
        0 reactions
        Last Post SEQadmin2  
        Working...