Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Sakti
    Junior Member
    • May 2011
    • 6

    #1

    Obtaining reference identical reads from a BAM file

    Hi guys,

    This forum is awesome. I recently just started using software for seq data analysis. One question I have right now is how can I obtain the reads that map with 100% identity (no mismatches) to a reference genome. I have BAM files available, and was thinking that SAMTools is the way to do it, but I haven't figured it out yet.

    If someone could point me to a useful reference or give me some guidance I'll be extremely grateful.

    Thanks!

    -Sakti
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    You could use grep on the .sam file. There are a couple of entries that might be in your sam file that would indicate what the distance is between your read and your reference, and what the actual differences are between your read and your reference. If the NM value equals 0, then there are no differences (though you might also want to check the CIGAR entry, to see that there was no clipping of the read).

    Comment

    • Sakti
      Junior Member
      • May 2011
      • 6

      #3
      Thanks for the help!! I ended up using MUMmer to get all identical sequences. I guess it was more straightforward than using the BAM alignments...

      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
      27 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
      36 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      43 views
      0 reactions
      Last Post SEQadmin2  
      Working...