Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • int11ap1
    Member
    • Jan 2014
    • 16

    #1

    SNP density

    Hi guys,

    This is my first thread here in this forum. I hope I'm writing this question into the correct category!

    Well, I have called variants with samtools mpileup, where:

    MAPQ=20 # min map quality
    BASEQ=20 # min base quality

    and then filtered them by:

    MINCOV=5 # min coverage
    MAXCOV=30 # maximum coverage

    Now, I have to look for the SNP density within the region sequenced. For that, I obtain the depth file (samtools depth).

    awk '{nucleotides++} END {print nucleotides}' depthfile.txt
    #In order to know the real length.

    It should be as simple as divide the number of SNP by the length. However, doing that I would obtain a wrong number of SNP/kb, because I've filtered SNPs by quality and coverage.

    So, am I correct if I should filter the depth file by coverage? Quality as well? Or not?

    Thanks a lot, guys.
  • TiborNagy
    Senior Member
    • Mar 2010
    • 329

    #2
    You do not need to deal with the depth file. All you need is the VCF file (produced by mpileup and bcftools, but other variant calling pipelines also produces this output type). This contains the depth information and quality. You should filter SNPs by quality and depth.

    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
      ...
      Today, 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, Today, 05:39 AM
    0 responses
    10 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, Yesterday, 09:56 AM
    0 responses
    12 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 10-09-2026, 11:14 AM
    0 responses
    26 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 09-29-2026, 09:51 AM
    0 responses
    77 views
    0 reactions
    Last Post SEQadmin2  
    Working...