Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • bjchen
    Junior Member
    • Jan 2012
    • 9

    #1

    question about samtools mpileup -6

    Hi,

    Can anyone please tell me when to use this option? I am a bit confused about this. I have sequence data with Illumina 1.8 encoding and have aligned them to generate bam files. In the documentation of mpileup, it says

    -6 Assume the quality is in the Illumina 1.3+ encoding.

    But I don't know if bam files have such encoding issues..

    Thanks!!!
  • Kennels
    Senior Member
    • Feb 2011
    • 149

    #2
    I think it means if you have the qscores in the former illumina format then use this option. Since your data is based on Illumina 1.8+ which i believe is in the Sanger qscore format already, then you don't need to use it.
    Here is a reference explaining qscore differences:

    FASTQ has emerged as a common file format for sharing sequencing read data combining both the sequence and an associated per base quality score, despite lacking any formal definition to date, and existing in at least three incompatible variants. ...

    Comment

    • bjchen
      Junior Member
      • Jan 2012
      • 9

      #3
      That's what I guessed, although still got confused by the "+" in the "1.3+"...
      Thanks!

      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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 12:22 PM
      0 responses
      12 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-11-2026, 10:35 AM
      0 responses
      13 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-06-2026, 07:41 AM
      0 responses
      31 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-03-2026, 10:13 AM
      0 responses
      48 views
      0 reactions
      Last Post SEQadmin2  
      Working...