Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • edit RGID in header

    I assigned RGID's to 4 different sets of files. I labeled them L1, L2, L3, L4 to indicate which lane they were from. I was having issues after samtools merge and I think the problem is that the first in.bam header overwrote the other headers (this is in the samtools manual). Basically I have orphan reads now because they have a RGID that isn't in the header. All the other RG tags are identical in the bam files. I was told that I needed to add the other ID's to my header in the merged file. So I guess the header needs to say something like RGID: L1, L2, L3, L4 for it to work properly but I don't think you can put comma's. I don't really know how to reformat text files and on a scale of 1-10 in programming knowledge, I would put myself at a 2. Can someone please give me an example code for how to edit this header? I will attach the header of my existing file below if that helps.
    Attached Files

  • #2
    I think various RGs need to be on separate lines.
    You can use text editor to get the header you want, no "programming" involved using gedit/vim/emacs.
    It you did want to program, using the Unix tools sed,grep,cat and so in a script could solve the problem.
    When you get the header you want, try the samtools "reheader" option.

    Comment


    • #3
      In the future you might want to use Picard Tools MergeSamFiles. It merges header information in addition to the alignment portions of the BAM files.

      Comment


      • #4
        Originally posted by Richard Finney View Post
        I think various RGs need to be on separate lines.
        You can use text editor to get the header you want, no "programming" involved using gedit/vim/emacs.
        It you did want to program, using the Unix tools sed,grep,cat and so in a script could solve the problem.
        When you get the header you want, try the samtools "reheader" option.
        I think I wasn't clear when I said I couldn't program very well. I actually meant I couldn't program as well as do what you are describing.

        Comment


        • #5
          Originally posted by shawpa View Post
          I think I wasn't clear when I said I couldn't program very well. I actually meant I couldn't program as well as do what you are describing.
          There's no programming involved. You need to edit the header to add lines for samples L2, L3, and L4.

          Right now your header has only L1:
          Code:
          @RG     ID:L1   PL:ILLUMINA     PU:D0DHVACXX    LB:ryan SM:ryan
          You need all four in the header, and they need to have different sample names (SM):

          Code:
          @RG     ID:L1   PL:ILLUMINA     PU:D0DHVACXX    LB:ryan SM:ryan1
          @RG     ID:L2   PL:ILLUMINA     PU:D0DHVACXX    LB:ryan SM:ryan2
          @RG     ID:L3   PL:ILLUMINA     PU:D0DHVACXX    LB:ryan SM:ryan3
          @RG     ID:L4   PL:ILLUMINA     PU:D0DHVACXX    LB:ryan SM:ryan4
          You could use samtools view -h to make a sam file from the merged bam and then edit that file directly, but that's probably a bad idea since the file might be huge.

          The method Richard Finney suggests is to use samtools reheader:
          Code:
          samtools view -H file.bam > header.txt
          ...edit header.txt using any text editor...
          samtools reheader header.txt file.bam > file.fixedheader.bam

          Comment


          • #6
            Thanks so much. This is exactly what I needed.

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Current Approaches to Protein Sequencing
              by seqadmin


              Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
              04-04-2024, 04:25 PM
            • seqadmin
              Strategies for Sequencing Challenging Samples
              by seqadmin


              Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
              03-22-2024, 06:39 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 04-11-2024, 12:08 PM
            0 responses
            25 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 10:19 PM
            0 responses
            28 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 09:21 AM
            0 responses
            24 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-04-2024, 09:00 AM
            0 responses
            52 views
            0 likes
            Last Post seqadmin  
            Working...
            X