Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • One Question about Varscan

    Hi,I have one question about varscan.

    There is one position,I think somatic_status should be Somatic,but the result show it reference.Is there anybody can explain it ?Thank you!

    chr position T G 26 1 3.7% T 40 10 20% K Reference 1.0 0.04709966879527449 15 25 4 6

  • #2
    Hi,

    I don't have an answer but something similar:
    chr1 16946535 T C 2 16 88,89% C 8 6 42,86% Y Germline 1.0 0.007696151924037949 1 7 1 5
    The "somatic p_vlaue" is 0.007 and I chose the threshold as 0.05 so it should be classified as "Somatic"...

    Comment


    • #3
      Hello LiLin,

      There are a few criteria used to determine the somatic status of a variant. In your case, it seems most likely that --somatic-p-value was something lower than 0.47, so the variant did not meet the threshold to be called Somatic. Would you mind providing three things?
      1.) The VarScan version you're running
      2.) The command you used including all parameters
      3.) The normal and tumor pileup/mpileup for that chromosome position (it's fine if you alter the chromosome name or position; we need the depth, bases, and qualities).

      Jane, in your example, the variant is not called Somatic because the variant allele frequency is higher in normal (89%) than in tumor (43%).

      Comment


      • #4
        Hi,dkoboldt.
        1.)VarScan.v2.2.5.jar
        2.)Parameters:--min-coverage 10 --min-coverage-normal 10 --min-coverage-tumor 10 --min-var-freq 0.1 --min-freq-for-hom 0.75 --somatic-p-value 0.0001 --min-avg-qual 0 --validation 1
        3.)
        tumor mpileup:
        chr7 126351120 t 50 g,.,gg,.,,,..g,,,,GG..G,,.,,,,...,,...,,,,,g,G..g, 6CDDCCDDDC%DECD%%D;<DC;C%DDDD%CEDCDEDD%DC%4CC;DDB%
        normal mpileup:
        chr7 126351120 t 27 .,$...,.,,,C.,.,,,.,....,,.. B%EDDDDD%C#DEE%E%DDDEDDCDAD

        Comment


        • #5
          Originally posted by dkoboldt View Post
          Jane, in your example, the variant is not called Somatic because the variant allele frequency is higher in normal (89%) than in tumor (43%).
          Code:
          chr1 16946535 T C 2 16 88,89% C 8 6 42,86% Y Germline 1.0 0.007696151924037949 1 7 1 5
          Dan, do you mean that if I had something like
          Code:
          0 100 50 50
          it would be classified as germline ?
          For me (but I am not biologist), it's a somatic mutation, as
          Code:
          0 100 100 0
          would be...
          Am I wrong?

          Comment


          • #6
            Originally posted by dkoboldt View Post
            Hello LiLin,

            There are a few criteria used to determine the somatic status of a variant. In your case, it seems most likely that --somatic-p-value was something lower than 0.47, so the variant did not meet the threshold to be called Somatic. Would you mind providing three things?
            1.) The VarScan version you're running
            2.) The command you used including all parameters
            3.) The normal and tumor pileup/mpileup for that chromosome position (it's fine if you alter the chromosome name or position; we need the depth, bases, and qualities).

            Jane, in your example, the variant is not called Somatic because the variant allele frequency is higher in normal (89%) than in tumor (43%).


            Thank you!
            Now I set --somatic-p-value 0.05,Then I find it.

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Essential Discoveries and Tools in Epitranscriptomics
              by seqadmin




              The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
              04-22-2024, 07:01 AM
            • 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

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, Yesterday, 08:47 AM
            0 responses
            16 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-11-2024, 12:08 PM
            0 responses
            60 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 10:19 PM
            0 responses
            60 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 09:21 AM
            0 responses
            54 views
            0 likes
            Last Post seqadmin  
            Working...
            X