Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • wenhuang
    Member
    • Feb 2010
    • 30

    #1

    what is a read group?

    Hi,

    I am sure this is a silly question, but what is a read group in bam files? A lane? a flow cell? a library? or any meaningful thing that can group reads together?

    Thanks!

    Wen
  • danielsbrewer
    Member
    • Feb 2009
    • 35

    #2
    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc

    Comment

    • rskr
      Senior Member
      • Oct 2010
      • 249

      #3
      I define the term read-group as a set of reads that are the result of the exact same wet lab protocol, from isolation of samples to attached barcodes and indexing. Informally I use the term read-group when referring to a GaIIx lane or HiSeq index.

      Do they use that same convention?

      Comment

      • weeseda
        Junior Member
        • Dec 2011
        • 5

        #4
        I've checked out the samtools man and other documents, but I'm still confussed on the read group line.

        I am looking at 3 populations each of 8 individuals and want to do some SNP calling and downstream analysis. All 24 individuls were barcoded and run in one illumina lane.

        To keep track of individuals and populations how would I set up the readgroup line? RG= population name and SM= individual (as below)? or is it even possible to keep track of both?

        Thanks in advance for any insight!

        rg.txt file for use with following command: samtools merge -rh rg.txt merged.bam *.bam

        @RG ID:Pop1 SM:27861 PL:Illumina
        @RG ID:Pop1 SM:27862 PL:Illumina
        @RG ID:Pop2 SM:27863 PL:Illumina
        @RG ID:Pop2 SM:27864 PL:Illumina
        @RG ID:Pop3 SM:27865 PL:Illumina
        @RG ID:Pop3 SM:27866 PL:Illumina
        .
        .
        .

        Comment

        • kmcarr
          Senior Member
          • May 2008
          • 1181

          #5
          Originally posted by weeseda View Post
          I've checked out the samtools man and other documents, but I'm still confussed on the read group line.

          I am looking at 3 populations each of 8 individuals and want to do some SNP calling and downstream analysis. All 24 individuls were barcoded and run in one illumina lane.

          To keep track of individuals and populations how would I set up the readgroup line? RG= population name and SM= individual (as below)? or is it even possible to keep track of both?

          Thanks in advance for any insight!

          rg.txt file for use with following command: samtools merge -rh rg.txt merged.bam *.bam

          Code:
          @RG	ID:Pop1	SM:27861	PL:Illumina
          @RG	ID:Pop1	SM:27862	PL:Illumina
          @RG	ID:Pop2	SM:27863	PL:Illumina
          @RG	ID:Pop2	SM:27864	PL:Illumina
          @RG	ID:Pop3	SM:27865	PL:Illumina
          @RG	ID:Pop3	SM:27866	PL:Illumina
          .
          .
          .
          Each read group you define must have a unique ID. Your example does not, it uses each ID (Pop1, Pop2, Pop3) twice. Try something like this:

          Code:
          @RG	ID:1	SM:Pop1-27861	PL:Illumina
          @RG	ID:2	SM:Pop1-27862	PL:Illumina
          @RG	ID:3	SM:Pop2-27863	PL:Illumina
          @RG	ID:4	SM:Pop2-27864	PL:Illumina
          @RG	ID:5	SM:Pop3-27865	PL:Illumina
          @RG	ID:6	SM:Pop3-27866	PL:Illumina

          Comment

          • fhtyert
            Junior Member
            • Jun 2022
            • 1

            #6
            Great work!



            basket random

            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
            23 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
            42 views
            0 reactions
            Last Post SEQadmin2  
            Working...