Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dina
    Member
    • Sep 2009
    • 34

    #1

    blast of the 454 reads

    Hi
    I want to find virus integration sites in a genome we sequenced. Is it more reasonable to blast the resulted contigs or maybe blast the reads themselves would be more productive?
    Do you have any other idea how to "catch" those integration sites?
    Thank you!
  • bioinfosm
    Senior Member
    • Jan 2008
    • 483

    #2
    Assembly into contigs will iron out some of 454's noise and give better results I guess. BLAT might be a faster option than blast!
    --
    bioinfosm

    Comment

    • dina
      Member
      • Sep 2009
      • 34

      #3
      Blat

      Thank you. Can you explain to me how do I run BLAT for mant contigs as abatch? how I can do that via the command line and not on the web? Thank you!

      Comment

      • bioinfosm
        Senior Member
        • Jan 2008
        • 483

        #4
        You may try UCSC with some of your contigs to see how it works


        Then probably install blat locally and use their command line..
        --
        bioinfosm

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
          by SEQadmin2




          NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...
          Today, 06:46 AM
        • 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

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 10-28-2026, 09:57 AM
        0 responses
        22 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-28-2026, 09:51 AM
        0 responses
        14 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 11:13 AM
        0 responses
        67 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-22-2026, 10:48 AM
        0 responses
        47 views
        0 reactions
        Last Post SEQadmin2  
        Working...