Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • aew
    Junior Member
    • Aug 2012
    • 1

    #1

    VCF NC Format

    Hi,

    I ran VARSCAN2 mpileup2snp to call SNPs and generated a vcf file.

    However, I noticed a strange thing about the NC flag. This is apparently INFO=<id=nc,number=1,type=integer,description="number of="" samples="" not="" called"="">

    However, I see

    Code:
    TR43100|c0_g1_i1    792 .   T   C   .   PASS    ADP=0;WT=1;HET=0;HOM=1;NC=17    GT:GQ:SDP:DP:RD:AD:FREQ:PVAL:RBQ:ABQ:RDF:RDR:ADF:ADR    ./.:.:0 ./.:.:0 ./.:.:0 ./.:.:1 ./.:.:0 ./.:.:1 ./.:.:0 ./.:.:0 ./.:.:1 0/0:10:5:5:5:0:0%:1E0:38:0:0:5:0:0  ./.:.:0 ./.:.:1 ./.:.:1 1/1:7:2:2:0:2:100%:1.6667E-1:0:33:0:0:1:1   ./:.:0  ./:.:0  ./:.:0  ./:.:0  ./:.:0
    This has NC=17 and I can see from the 19 samples 2 have been called. This seems correct.

    Code:
    TR43100|c1_g1_i1    351 .   T   C   .   PASS    ADP=0;WT=1;HET=1;HOM=0;NC=17    GT:GQ:SDP:DP:RD:AD:FREQ:PVAL:RBQ:ABQ:RDF:RDR:ADF:ADR    ./:.:0  ./:.:0  ./:.:0  ./:.:0  ./:.:0  ./:.:1  ./:.:0  ./:.:0  ./:.:0  ./:.:2  ./:.:0  ./:.:0  ./:.:0  0/1:6:4:4:2:2:50%:2.1429E-1:40:38:2:0:1:1   ./:.:0  ./:.:0  ./:.:0  ./:.:0  ./:.:0
    This has NC=17 abut I can only see one sample that has been called? What have I missed, why isn't NC=18 here?

    And it says WT=1. Where is the WT? This should be 0/0

    And also
    Code:
    TR43100|c0_g1_i1 763 . G A . PASS ADP=0;WT=2;HET=0;HOM=1;NC=16 GT:GQ:SDP:DP:RD:AD:FREQ:PVAL:RBQ:ABQ:RDF:RDR:ADF:ADR ./.:.:0 ./.:.:0 ./.:.:0 1/1:13:3:3:0:3:100%:5E-2:0:39:0:0:0:3 ./.:.:0 ./.:.:1 ./.:.:0 ./.:.:0 ./.:.:1 0/0:6:3:3:3:0:0%:1E0:40:0:0:3:0:0 ./.:.:0 ./.:.:1 ./.:.:1 ./.:.:2 ./.:.:0 ./.:.:0 ./.:.:0 ./.:.:0 ./.:.:0
    Where are the 2 WT? I can only see 1 0/0
    Last edited by GenoMax; 03-07-2016, 08:12 AM. Reason: added CODE tags to improve readability
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    For reference/cross-posted: https://www.biostars.org/p/180308/

    Comment

    Latest Articles

    Collapse

    • SEQadmin2
      Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
      by SEQadmin2



      CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

      Despite this, “CRISPR helped turn genome editing from a specialized technique into
      ...
      07-31-2026, 11:01 AM
    • SEQadmin2
      Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
      by SEQadmin2


      Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

      The systematic characterization of the human proteome has
      ...
      07-20-2026, 11:48 AM

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by SEQadmin2, Yesterday, 12:22 PM
    0 responses
    12 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-11-2026, 10:35 AM
    0 responses
    14 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    31 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    50 views
    0 reactions
    Last Post SEQadmin2  
    Working...