Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • lchang1101
    Junior Member
    • Apr 2012
    • 2

    #1

    samtools mpileup did not call variant

    I used samtools mpileup and bcftools to call variants in my RNA-Seq data. At one locus, I have 10 reads that are different from the ref sequence (DP4=32,21,5,5), but bcftools did not call this variant.

    3 13812321 . T . 47 . DP=65;VDB=0.0190;AF1=0;AC1=0;DP4=32,21,5,5;MQ=20;FQ=-44;PV4=0.73,1,1,1 PL: DP:SP 0:63:1

    I tried to change the -p value from the default 0.5 to 0.6, 0.7, 0.8 and 0.9 but still none of them called this variant. I understand that 10 reads in 65 reads is a low fraction, but is there anyway to make bcftools less stringent? I know I can just print out info for every locus and do my own filtering but I was just wondering if there are other parameters of bcftool tat I can modify. Thanks!
  • vivek_
    PhD Student
    • Jul 2012
    • 164

    #2
    Isn't Mapq=20 rather too low to confidently take the alignment at that position?

    Comment

    • lchang1101
      Junior Member
      • Apr 2012
      • 2

      #3
      Thank you for the reply. No, I dont think MQ=20 was the problem. Some of the called variants in my run had MQ as low as 16. Any other thoughts?

      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, 10:52 AM
      0 responses
      9 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      19 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-13-2026, 09:56 AM
      0 responses
      16 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-09-2026, 11:14 AM
      0 responses
      27 views
      0 reactions
      Last Post SEQadmin2  
      Working...