Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • 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

  • #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


    • #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


      • #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

        • seqadmin
          Current Approaches to Protein Sequencing
          by seqadmin


          Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
          04-04-2024, 04:25 PM
        • seqadmin
          Strategies for Sequencing Challenging Samples
          by seqadmin


          Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
          03-22-2024, 06:39 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by seqadmin, 04-11-2024, 12:08 PM
        0 responses
        18 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 10:19 PM
        0 responses
        22 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-10-2024, 09:21 AM
        0 responses
        17 views
        0 likes
        Last Post seqadmin  
        Started by seqadmin, 04-04-2024, 09:00 AM
        0 responses
        48 views
        0 likes
        Last Post seqadmin  
        Working...
        X