Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • wangzkai
    Member
    • Feb 2010
    • 11

    #1

    SNP quality score in Samtools pileup

    Hi,

    I was examining the pileup by Samtools at a particular base of interest:

    X 131016403 G G 103 0 60 53 T$T,,.t.....T.TT,,,..,.t,,...,t,t,tTT,.TT..T..Tt,,T,,t BFGGAGCEFEEE<B-GGGAGGFGGGGGG?GGFGGGGGBEGFGGGEGEFDGGEF

    It looks like a clear heterozygous position with good coverage and decent base qualities, however it got a SNP quality score of 0 and a homozygous genotype call. Is there any possible explanation for this?

    The data are from 75x2 PE reads and alignment was done using ELANDv2. Any help on this will be highly appreciated. Thanks!
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    Originally posted by wangzkai View Post
    Hi,

    I was examining the pileup by Samtools at a particular base of interest:

    X 131016403 G G 103 0 60 53 T$T,,.t.....T.TT,,,..,.t,,...,t,t,tTT,.TT..T..Tt,,T,,t BFGGAGCEFEEE<B-GGGAGGFGGGGGG?GGFGGGGGBEGFGGGEGEFDGGEF

    It looks like a clear heterozygous position with good coverage and decent base qualities, however it got a SNP quality score of 0 and a homozygous genotype call. Is there any possible explanation for this?

    The data are from 75x2 PE reads and alignment was done using ELANDv2. Any help on this will be highly appreciated. Thanks!
    Maybe the mapping qualities for the variant reads are low?

    Comment

    • martian_bob
      Member
      • Feb 2010
      • 11

      #3
      Originally posted by nilshomer View Post
      Maybe the mapping qualities for the variant reads are low?
      This is exactly what I found when I came across the same puzzling situation. Converting the data to BAM format and then visualizing it in IGV showed me that the apparently heterozygous SNP was getting all of its heterozygous bases from the low-quality ends of the reads - the SNP never once showed up in the beginning or middle of a read, only when it was within 7 nt of the end.

      Odd? Yes. But if it were a true SNP, you'd expect to find it in half of the reads regardless of position.

      Comment

      • juan
        Member
        • Aug 2009
        • 14

        #4
        Yes that is the problem with SAMtools. The majority of variants are in the 2nd half of the read, hence you have lots of false positives.

        Comment

        • christophpale
          Member
          • May 2010
          • 16

          #5
          Does anyone have a code that can print out the positions within each of the reads where a given snp exist?
          Last edited by christophpale; 07-21-2010, 03:11 AM.

          Comment

          • pengchy
            Senior Member
            • Feb 2009
            • 116

            #6
            Is there any more explanation?
            I have found the following contrast examples:
            Code:
            scaffold2410 23912 G S 6 6 37 123 c,,,,,,,,,,,,,,,,,,,,ccc,,cc,,,,,,,,,,,,,ccc,,cc,cccc,,cc,,,,,,,cc,,c,cc,c,,c,,,,c,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,, HHHHHHHHHHHHHHHHHFEHJCCHJEIHHHHHBHHHHHHFHHHHGHHHHHHHHHHCHHHHHHHJFFGJJJJHJHHHHHHHHHHHHHHHHHHHHH<HHHHHGHHHHGHHGHHHGHHGH<GJJIA
            and :
            Code:
            scaffold12030   25942   A       R       37      44      25      44      gggggg,gg,g,,,,,,,ggggggggggggggggggggggggg,    HHHHHHGHHGHEHGHHHHHFHHHHHHHHHHGHBFHHHHHHHHHJ
            Both of these two examples have similar reads quality and mapped on the reverse strand of reference, but with different "SNP quality", how these results produced?

            Anyone who can give me any suggestions will be highly appreciated.

            We have estimated the heterozygosis based on the results that filtered by VarFilter, obviously, we have under estimated the heterozygosis level.
            Last edited by pengchy; 09-21-2011, 06:37 AM.

            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
            • SEQadmin2
              Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
              by SEQadmin2



              Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
              ...
              07-09-2026, 11:10 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, Yesterday, 10:13 AM
            0 responses
            14 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-31-2026, 02:55 AM
            0 responses
            29 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-24-2026, 12:17 PM
            0 responses
            22 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 07-23-2026, 11:41 AM
            0 responses
            21 views
            0 reactions
            Last Post SEQadmin2  
            Working...