Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • mstagliamonte
    Member
    • Feb 2013
    • 33

    #1

    Samtools and intrasample diversity

    Hi, Seqanswers community,

    I need some help with my variant calling.

    I am dealing with a monocellular organisms, and I am expecting intrasample diversity due to multiclonality. This could mean that the real allele frequency is not necessarily 50% each (in case of biallelic snp)
    After calling variants with samtools/bcftools, I would like to determine intrasample allele frequencies for each individual sample. Is there a way I can quantify the support for each allele with samtools (probably using the sam or bam files) or any similar program?

    Hope what I've written makes sense, please let me know if you need any more information.

    Thanks,
    Max
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    I'd use samtools to make a pileup file, and then parse the line of the pileup for how many ref and alt letters you see.

    Comment

    • mstagliamonte
      Member
      • Feb 2013
      • 33

      #3
      Thanks, I'll try

      Regards,
      Max

      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
      19 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, Yesterday, 10:48 AM
      0 responses
      18 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
      42 views
      0 reactions
      Last Post SEQadmin2  
      Working...