Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • unique379
    Member
    • Aug 2012
    • 27

    #1

    Sam quality flag

    Hello all,

    heading just a quick reply

    I aligned my color-space fastq by bowtie 1 and got sam as output. But in my all mapped reads i have 255 instead any quality information, that means quality information is absent. However, my question is..

    1) Why its happened ??
    2) Lacking this quality information would really hurt for my further analysis by this sam ??? (lets say DE analysis or any downstream analysis )

    Thanks in advance
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    With bowtie1 (as with earlier versions of tophat), a MAPQ of 255 means a unique alignment. The other MAPQ scores for bowtie1 are 0, 1, 2, and 3, which indicate different levels of multiple mappings. For DE, you just care about unique alignments, so just filter by MAPQ accordingly.

    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, 10:35 AM
    0 responses
    10 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    28 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    46 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    48 views
    0 reactions
    Last Post SEQadmin2  
    Working...