Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • efoss
    Member
    • Jul 2011
    • 98

    #1

    basic question about read groups

    I have run into problems in which GATK complains that my bam file is malformed because it's missing read group information. I have fixed this by going back to the "sampe" step in bwa and adding a "-r" option and today for the first time I'm trying to fix this with PicardTools' "AddOrReplaceReadGroups" tool. But these tools take quite a long time to run. Would there be anything wrong with simply adding the read group information manually at the top of a sam file and then converting that sam file to a bam file? I guess I don't know if there is anything more to the read group than a line near the beginning of a sam file or whether instead adding read group information with a bwa tool or a PicardTools tool is doing something more involved (e.g. somehow embedding read group information in multiple places in the sam/bam file).

    Thank you.

    Eric
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    In addition to the @RG line in the SAM header, every single read belonging to that read group has to declare this in its tags - and that part means adding this requires a lot of IO and will be comparatively slow.

    If all you want to do is add some information to an existing read group, you just need to edit the SAM header. Using samtools reheader let's you modify this efficiently in a BAM file.
    Last edited by maubp; 10-19-2011, 12:12 AM. Reason: Typo

    Comment

    • efoss
      Member
      • Jul 2011
      • 98

      #3
      Originally posted by maubp View Post
      In addition to the @RG line in the SAM header, every single read belonging to that read group has to declare this in its tags - and that part means adding this requires a lot of IO and will be comparatively slow.

      If all you want to do is add some information to an existing read group, you just need to edit the SAM header. Using samtools reheader let's you modify this efficiently in a BAM file.
      Thanks. That makes sense.

      Eric

      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
      14 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 08-11-2026, 10:35 AM
      0 responses
      16 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
      50 views
      0 reactions
      Last Post SEQadmin2  
      Working...