Unconfigured Ad

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

    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
        Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
        by SEQadmin2



        Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
        ...
        07-09-2026, 11:10 AM
      • SEQadmin2
        Cancer Drug Resistance: The Lingering Barrier to Rising Survival
        by SEQadmin2



        Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

        There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
        07-08-2026, 05:17 AM
      • GATTACAT
        Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
        by GATTACAT
        Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
        07-01-2026, 11:43 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 07-13-2026, 10:26 AM
      0 responses
      24 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-09-2026, 10:04 AM
      0 responses
      33 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-08-2026, 10:08 AM
      0 responses
      21 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-07-2026, 11:05 AM
      0 responses
      34 views
      0 reactions
      Last Post SEQadmin2  
      Working...