Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • cliff
    Member
    • Oct 2009
    • 41

    Samtools - pileup format question - "*" is a deletion

    I am using SAMtools pileup to make indel and snp calls. In the read bases column (9th), there is a "*". Similar question can be found here
    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc


    Here are some columns I picked from one position:

    CHR POSITION Ref Base Genotype Reads Number
    chr10 23172627 g S 31

    Read Bases
    c$t$c$a$c$c$.a,c,,**,,$,$,,$,,.,,,,,,,,,

    My question is

    I counted the allele frequency for each base and I found A has 2 reads, C has 5 reads, G has 21 reads, and T has 1 read. But the total number of reads here are 31. Since the two "*" represents two deletions, I should count "*" as which base?

    Thanks
  • Pepe
    Member
    • Mar 2009
    • 30

    #2
    Hi,

    commas and periods represent reads with nucleotides that match the reference, that's why it says you have 31 of them.

    I'm not sure about the **.

    Comment

    • nilshomer
      Nils Homer
      • Nov 2008
      • 1283

      #3
      Originally posted by cliff View Post
      I am using SAMtools pileup to make indel and snp calls. In the read bases column (9th), there is a "*". Similar question can be found here
      Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc


      Here are some columns I picked from one position:

      CHR POSITION Ref Base Genotype Reads Number
      chr10 23172627 g S 31

      Read Bases
      c$t$c$a$c$c$.a,c,,**,,$,$,,$,,.,,,,,,,,,

      My question is

      I counted the allele frequency for each base and I found A has 2 reads, C has 5 reads, G has 21 reads, and T has 1 read. But the total number of reads here are 31. Since the two "*" represents two deletions, I should count "*" as which base?

      Thanks
      An easy way to determine the two reads with "*" would be to look at that position in a genome viewer (i.e. IGV or "samtools tview").

      Comment

      • sunhh
        Member
        • Jun 2012
        • 18

        #4
        Hi,
        If you check the previous lines of this position "chr10 23172627", you will find some site that
        has a deletion there. And this deletion makes a '*' label in the corresponding site here.
        So, it means there are two reads supporting a deletion at this site.

        Best.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by SEQadmin2


          I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

          Here are nine questions we think about, in roughly the order they matter, before...
          06-18-2026, 07:11 AM
        • SEQadmin2
          From Collection to Sequencing: Why Sample Preparation and Preservation Define Sequencing Data
          by SEQadmin2


          Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.


          The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
          ...
          06-02-2026, 10:05 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 05:37 AM
        0 responses
        5 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-26-2026, 11:10 AM
        0 responses
        16 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-17-2026, 06:09 AM
        0 responses
        50 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-09-2026, 11:58 AM
        0 responses
        110 views
        0 reactions
        Last Post SEQadmin2  
        Working...