Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Why my variant is found if AD alt = 0 in my vcf file ?

    Hi,

    My problem is about intepretation of vcf file for indels variation, and particulary, about AD tag (Allele Depth) find in the last column. I obtained my vcf file after processing "Unified Genotyper / Hard filtering" method as recommended by GATK. And as you can read in my example, AD tag ==> 154,0 (DP=171). (AD tag means allelic depths for the ref and alt alleles in the order listed).

    chr6 36485587 . GAATGTCACGCTCCGC G 760.73 PASS AC=1;AF=0.500;AN=2;DP=171;FS=0.000;MLEAC=1;MLEAF=0.500;MQ=58.10;MQ0=0;QD=0.30 GT:ADP:GQ:PL 0/1:154,0:171:99:798,0,25782
    I don't understand how the variant can be detected if the AD Alt = 0 ?


    Anybody could explain me please ?


    Best,

    Sam
    Last edited by Sam64; 06-26-2014, 01:13 AM.

  • #2
    GATK forum

    On GATK forum, you can read :

    http://www.broadinstitute.org/gatk/g...eBySample.html

    [...] Please note, however, that the AD isn't necessarily calculated exactly for indels. Only reads which are statistically favoring one allele over the other are counted. Because of this fact, the sum of AD may be different than the individual sample depth, especially when there are many non-informative reads.

    Because the AD includes reads and bases that were filtered by the caller and in case of indels is based on a statistical computation, one should not base assumptions about the underlying genotype based on it; instead, the genotype likelihoods (PLs) are what determine the genotype calls.[...]
    Last edited by Sam64; 06-26-2014, 02:01 AM.

    Comment


    • #3
      upupupupupupupupupup

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Advancing Precision Medicine for Rare Diseases in Children
        by seqadmin




        Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
        12-16-2024, 07:57 AM
      • seqadmin
        Recent Advances in Sequencing Technologies
        by seqadmin



        Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

        Long-Read Sequencing
        Long-read sequencing has seen remarkable advancements,...
        12-02-2024, 01:49 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 12-17-2024, 10:28 AM
      0 responses
      25 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-13-2024, 08:24 AM
      0 responses
      42 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-12-2024, 07:41 AM
      0 responses
      28 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 12-11-2024, 07:45 AM
      0 responses
      42 views
      0 likes
      Last Post seqadmin  
      Working...
      X