Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • mrxcm3
    Junior Member
    • Oct 2010
    • 9

    #1

    Samtools 'import' and lost read group header

    I am pretty new to manipulating NextGenSeq datasets, so my apologies if this question is trivial!

    I want to format my .bam files so I can use them in GATK for SNP calling. Although my .bam files have all the necessary 'read group' information, they are sorted in an lexicographical order - which will not work with GATK.

    However, if I resort my .bam so the headers are replaced by the reference using;

    samtools import <your reference>.fai <your file>.sam <your file>.sorted_header.bam

    then my read group header disappears - and GATK wont work! Most annoying! Does anyone know of a way to either avoid this when resorting, or adding the '@RG' header afterwards?? Thanks
  • maubp
    Peter (Biopython etc)
    • Jul 2009
    • 1544

    #2
    Try "samtools reheader" to replace the BAM header.

    Comment

    • mrxcm3
      Junior Member
      • Oct 2010
      • 9

      #3
      Thanks maubp this has worked

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
        by SEQadmin2



        Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

        Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
        ...
        10-14-2026, 09:55 AM
      • SEQadmin2
        New Genomics Technologies Take Aim at Long-Standing Limits
        by SEQadmin2


        Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

        We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
        ...
        09-28-2026, 10:25 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 10-22-2026, 11:13 AM
      0 responses
      27 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 10:48 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      36 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      43 views
      0 reactions
      Last Post SEQadmin2  
      Working...