Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Strand Bias filtering

    Hello all,
    i run the variantCaller in germline_low_stringency mode with the default parameters

    the strand bias threshold for snp Strand Bias is 0.95, everything up that value is considered strand bias

    we did some calculations using Relative Strand Bias Formula

    We found some cases where this filter works bad, for instance when we have FSAF:2 FSAR:1 FSRR:10 FSRF:0, the STB is 0.916 and therefore accepted as variant. Or FSAF:1 FSAR:1 FSRR:20 FSRF:20 the STB is 0.5 and therefore accepted again. So... we accept that calls???

  • #2
    Originally posted by c_ro87 View Post
    Hello all,
    i run the variantCaller in germline_low_stringency mode with the default parameters

    the strand bias threshold for snp Strand Bias is 0.95, everything up that value is considered strand bias

    we did some calculations using Relative Strand Bias Formula

    We found some cases where this filter works bad, for instance when we have FSAF:2 FSAR:1 FSRR:10 FSRF:0, the STB is 0.916 and therefore accepted as variant. Or FSAF:1 FSAR:1 FSRR:20 FSRF:20 the STB is 0.5 and therefore accepted again. So... we accept that calls???
    Strand bias is not the only parameter to take into account to remove false positive. Alternate allele frequency, Alternate allele count, Mapping quality, position on the read can be very usefull to filter variants.

    Comment


    • #3
      For Amplicon data a strand bias seems to be much more frequent than for Exome sequencing. So maybe filters should not be quite as strict. Maybe it is enough to check if a
      variant is found on both strands, or at least one percent on each strand. On the other hand
      i analyzed one sample where there was a significant bias for amplicon data and the strand bias was also found on exome data for the same sample.

      The Mutascope publication (specifically the supplement) discusses the Amplicon strand bias problem in more detail: http://bioinformatics.oxfordjournals...rmatics.btt305

      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
      12 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
      59 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